Endre søk
Begrens søket
12 1 - 50 of 93
RefereraExporteraLink til resultatlisten
Permanent link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Treff pr side
  • 5
  • 10
  • 20
  • 50
  • 100
  • 250
Sortering
  • Standard (Relevans)
  • Forfatter A-Ø
  • Forfatter Ø-A
  • Tittel A-Ø
  • Tittel Ø-A
  • Type publikasjon A-Ø
  • Type publikasjon Ø-A
  • Eldste først
  • Nyeste først
  • Skapad (Eldste først)
  • Skapad (Nyeste først)
  • Senast uppdaterad (Eldste først)
  • Senast uppdaterad (Nyeste først)
  • Disputationsdatum (tidligste først)
  • Disputationsdatum (siste først)
  • Standard (Relevans)
  • Forfatter A-Ø
  • Forfatter Ø-A
  • Tittel A-Ø
  • Tittel Ø-A
  • Type publikasjon A-Ø
  • Type publikasjon Ø-A
  • Eldste først
  • Nyeste først
  • Skapad (Eldste først)
  • Skapad (Nyeste først)
  • Senast uppdaterad (Eldste først)
  • Senast uppdaterad (Nyeste først)
  • Disputationsdatum (tidligste først)
  • Disputationsdatum (siste først)
Merk
Maxantalet träffar du kan exportera från sökgränssnittet är 250. Vid större uttag använd dig av utsökningar.
  • 1. Afewerki, Samson
    et al.
    Alimohammadzadeh, Rana
    Osong, Sinke H.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Engstrand, Per
    Córdova, Armando
    Sustainable Design for the Direct Fabrication and Highly Versatile Functionalization of Nanocelluloses2017Inngår i: Global Challenges, ISSN 2056-6646, Vol. 1, nr 7, artikkel-id 1700045Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This study describes a novel sustainable concept for the scalable direct fabrication and functionalization of nanocellulose from wood pulp with reduced energy consumption. A central concept is the use of metal-free small organic molecules as mediators and catalysts for the production and subsequent versatile surface engineering of the cellulosic nanomaterials via organocatalysis and click chemistry. Here, organoclick chemistry enables the selective functionalization of nanocelluloses with different organic molecules as well as the binding of palladium ions or nanoparticles. The nanocellulosic material is also shown to function as a sustainable support for heterogeneous catalysis in modern organic synthesis (e.g., Suzuki cross-coupling transformations in water). The reported strategy not only addresses obstacles and challenges for the future utilization of nanocellulose (e.g., low moisture resistance, the need for green chemistry, and energy-intensive production) but also enables new applications for nanocellulosic materials in different areas.

  • 2. Akansel, Serkan
    et al.
    Venugopal, Vijayaharan A.
    Kumar, Ankit
    Gupta, Rahul
    Brucas, Rimantas
    George, Sebastian
    Neagu, Alexandra
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Gubbins, Mark
    Andersson, Gabriella
    Svedlindh, Peter
    Effect of seed layers on dynamic and static magnetic properties of Fe65Co35 thin films2018Inngår i: Journal of Physics D: Applied Physics, ISSN 0022-3727, E-ISSN 1361-6463, Vol. 51, nr 30, artikkel-id 305001Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Fe65Co35 thin films have been deposited on SiO2 substrates using sputtering technique with different choices of seed layer; Ru, Ni82.5Fe17.5, Rh, Y and Zr. Best soft magnetic properties were observed with seed layers of Ru, Ni82.5Fe17.5 and Rh. Adding these seed layers, the coercivity of the Fe65Co35 films decreased to values of around 1.5 mT, which can be compared to the value of 12.5 mT obtained for films deposited without seed layer. Further investigations were performed on samples with these three seed layers in terms of dynamic magnetic properties, both on as prepared and annealed samples, using constant frequency cavity and broadband ferromagnetic resonance measurements. Damping parameters of around 8.0 x 10(-3) and 4.5 x 10(-3) were obtained from in-plane and out-of-plane measurements, respectively, for the as prepared samples, values that were reduced to about 6.5 x 10(-3) and 4.0 x 10(-3) for annealed samples.

  • 3. Asfaw, Habtom D.
    et al.
    Roberts, Matthew R.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Younesi, Reza
    Valvo, Mario
    Nyholm, Leif
    Edstrom, Kristina
    Nanosized LiFePO4-decorated emulsion-templated carbon foam for 3D micro batteries: a study of structure and electrochemical performance2014Inngår i: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 6, nr 15, s. 8804-8813Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In this article, we report a novel 3D composite cathode fabricated from LiFePO4 nanoparticles deposited conformally on emulsion-templated carbon foam by a sot-gel method. The carbon foam is synthesized via a facile and scalable method which involves the carbonization of a high internal phase emulsion (polyHIPE) polymer template. Various techniques (XRD, SEM, TEM and electrochemical methods) are used to fully characterize the porous electrode and confirm the distribution and morphology of the cathode active material. The major benefits of the carbon foam used in our work are closely connected with its high surface area and the plenty of space suitable for sequential coating with battery components. After coating with a cathode material (LiFePO4 nanoparticles), the 3D electrode presents a hierarchically structured electrode in which a porous layer of the cathode material is deposited on the rigid and bicontinuous carbon foam. The composite electrodes exhibit impressive cyclability and rate performance at different current densities affirming their importance as viable power sources in miniature devices. Footprint area capacities of 1.72 mA h cm(-2) at 0.1 mA cm(-2) (lowest rate) and 1.1 mA h cm(-2) at 6 mA cm(-2) (highest rate) are obtained when the cells are cycled in the range 2.8 to 4.0 V vs. lithium.

  • 4. Asfaw, Habtom D.
    et al.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Nyholm, Leif
    Edström, Kristina
    Over-Stoichiometric NbO2 Nanoparticles for a High Energy and Power Density Lithium Microbattery2017Inngår i: chemnanomat, ISSN 2199-692X, Vol. 3, nr 9, s. 646-655Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Effective utilization of active materials in microbatteries can be enhanced by rational design of the electrodes. There is an increasing trend of using 3D electrodes that are coated in nanosized active materials to boost both energy and power densities. This article focuses on the fabrication of 3D electrodes based on monolithic carbon foams coated in over-stoichiometric NbO2 nanoparticles. The electrodes exhibit remarkable energy and power densities at various current densities when tested in lithium microbatteries. An areal capacity of around 0.7mAhcm(-2) and energy density up to 45mWhcm(-3) have been achieved. More than half of the areal capacity can be accessed at a current density of about 11mAcm(-2), with the corresponding energy and power densities being 21mWhcm(-3) and 1349mWcm(-3). These values are comparable to those of microsupercapacitors containing carbon and MnO2 nanomaterials. Furthermore, the electrochemical reversibility improves progressively upon cycling along with substantial increase in the charge transfer kinetics of the electrode. Based on impedance analyses almost a fourfold decrease in the charge transfer resistance has been observed over 25 cycles. Such enhancement of the electronic properties of NbO2 can account for the high electrochemical rate performance of the 3D electrodes.

  • 5. Barzegar, Hamid R.
    et al.
    Nitze, Florian
    Sharifi, Tiva
    Ramstedt, Madeleine
    Tai, Cheuk W.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Malolepszy, Artur
    Stobinski, Leszek
    Wagberg, Thomas
    Simple Dip-Coating Process for the Synthesis of Small Diameter Single-Walled Carbon Nanotubes-Effect of Catalyst Composition and Catalyst Particle Size on Chirality and Diameter2012Inngår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 116, nr 22, s. 12232-12239Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on a dip-coating method to prepare catalyst particles (mixture of iron and cobalt) with a controlled diameter distribution on silicon wafer substrates by changing the solution's concentration and withdrawal velocity. The size and distribution of the prepared catalyst particles were analyzed by atomic force microscopy. Carbon nanotubes were grown by chemical vapor deposition on the substrates with the prepared catalyst particles. By decreasing the catalyst particle size to below 10 nm, the growth of carbon nanotubes can be tuned from few-walled carbon nanotubes, with homogeneous diameter, to highly pure single-walled carbon nanotubes. Analysis of the Raman radial breathing modes, using three different Raman excitation wavelengths (488, 633, and 785 nm), showed a relatively broad diameter distribution (0.8-1.4 nm) of single-walled carbon nanotubes with different chiralities. However, by changing the composition of the catalyst particles while maintaining the growth parameters, the chiralities of single-walled carbon nanotubes were reduced to mainly four different types, (12, 1), (12, 0), (8, 5), and (7, 5), accounting for about 70% of all nanotubes.

  • 6. Barzegar, Hamid Reza
    et al.
    Nitze, Florian
    Malolepszy, Artur
    Stobinski, Leszek
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Wagberg, Thomas
    Water Assisted Growth of C-60 Rods and Tubes by Liquid-Liquid Interfacial Precipitation Method2012Inngår i: Molecules, ISSN 1420-3049, E-ISSN 1420-3049, Vol. 17, nr 6, s. 6840-6853Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    C-60 nanorods with hexagonal cross sections are grown using a static liquid-liquid interfacial precipitation method in a system of C-60/m-dichlorobenzene solution and ethanol. Adding water to the ethanol phase leads instead to C-60 tubes where both length and diameter of the C-60 tubes can be controlled by the water content in the ethanol. Based on our observations we find that the diameter of the rods/tubes strongly depends on the nucleation step. We propose a liquid-liquid interface growth model of C-60 rods and tubes based on the diffusion rate of the good C-60 containing solvent into the poor solvent as well as on the size of the crystal seeds formed at the interface between the two solvents. The grown rods and tubes exhibit a hexagonal solvate crystal structure with m-dichlorobenzene solvent molecules incorporated into the crystal structure, independent of the water content. An annealing step at 200 degrees C at a pressure <1 kPa transforms the grown structures into a solvent-free face centered cubic structure. Both the hexagonal and the face centered cubic structures are very stable and neither morphology nor structure shows any signs of degradation after three months of storage.

  • 7. Bhatt, Aarti Sripathi
    et al.
    Bhat, Denthaje Krishna
    Santosh, Mysore Sridhar
    Tai, Cheuk-wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för oorganisk kemi och strukturkemi.
    Chitosan/NiO nanocomposites: a potential new dielectric material2011Inngår i: Journal of Materials Chemistry, ISSN 0959-9428, E-ISSN 1364-5501, Vol. 21, nr 35, s. 13490-13497Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The study of electrochemical behavior of organic-inorganic nanocomposite materials remains a major challenge for application in energy storage devices. Here, new composite materials of chitosan and NiO nanoparticles have been fabricated. The NiO nanoparticles are well characterized by infrared spectroscopy, X-ray diffraction and transmission electron microscopy. The electrical properties of the films are studied by impedance spectroscopy at different temperatures; and thereby permittivity, electric modulus and conductivity data are obtained. By studying the variations in permittivity and electric modulus spectra with respect to applied frequency signal and temperature, the ionic conductivity of the material is investigated. The Correlated Barrier Hopping model is employed to understand the conduction mechanism. An admirable conductivity of 1.4 x 10(-2) S cm(-1) is obtained for a nanocomposite with 4 wt% NiO content. The activation energies of the composite films decrease with increase in NiO content, from 16.5 to 4.8 kJ mol(-1).

  • 8.
    Bruneau, Alexandre
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Gustafson, Karl P. J.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Yuan, Ning
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK). Swedish University of Agricultural Sciences, Sweden.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Persson, Ingmar
    Zou, Xiaodong
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bäckvall, Jan-E.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Synthesis of Benzofurans and Indoles from Terminal Alkynes and Iodoaromatics Catalyzed by Recyclable Palladium Nanoparticles Immobilized on Siliceous Mesocellular Foam2017Inngår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 23, nr 52, s. 12886-12891Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Herein, we report on the utilization of a heterogeneous catalyst, consisting of Pd nanoparticles supported on a siliceous mesocellular foam (Pd-0-AmP-MCF), for the synthesis of heterocycles. Reaction of o-iodophenols and protected o-iodoanilines with acetylenes in the presence of a Pd nanocatalyst produced 2-substituted benzofurans and indoles, respectively. In general, the catalytic protocol afforded the desired products in good to excellent yields under mild reaction conditions without the addition of ligands. Moreover, the structure of the reported Pd nanocatalyst was further elucidated with extended X-ray absorption fine-structure spectroscopy, and it was proven that the catalyst could be recycled multiple times without significant loss of activity.

  • 9.
    Chamoun, Mylad
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Brant, William R.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Karlsson, Gunder
    Noréus, Dag
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Rechargeability of aqueous sulfate Zn/MnO2 batteries enhanced by accessible Mn2+ ions2018Inngår i: Energy storage materials, ISSN 2405-8289, Vol. 15, s. 351-360Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The Zn/MnO2 battery is safe, low cost and comes with a high energy density comparable to Li-ion batteries. However, irreversible spinel phases formed at the MnO2 electrode limits its cyclability. A viable solution to overcome this inactive phase is to use an aqueous ZnSO4-based electrolyte, where pH is mildly acidic leading to a different reaction mechanism. Most importantly, the addition of MnSO4 achieves excellent cyclability. How accessible Mn2+ ions in the electrolyte enhances the reversibility is presented. With added Mn2+, the capacity retention is significantly improved over 100 cycles. Zn2+ insertion plays an important role on the reversibility and a hydrated layered Zn-buserite structure formed during charge is reported. Furthermore, Zn4SO4(OH)(6) center dot 5H(2)O precipitates during discharge but is not involved in the electrochemical reaction. This precipitate both buffers the pH and partly insulates the surface. Described in operando study show how the phase transformations and the failure mechanisms depend on the presence of Mn2+-ions in the electrolyte. These results give insight necessary to improve this battery further to make it a worthy contender to the Li-ion battery in large scale energy storage solutions.

  • 10.
    Deiana, Luca
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Jiang, Yan
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Palo-Nieto, Carlos
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Afewerki, Samson
    Incerti-Pradillos, Celia A.
    Verho, Oscar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Johnston, Eric V.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Córdova, Armando
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi. Mid Sweden University, Sweden.
    Combined Heterogeneous Metal/Chiral Amine: Multiple Relay Catalysis for Versatile Eco-Friendly Synthesis2014Inngår i: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 53, nr 13, s. 3447-3451Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Herein is described a versatile and broad synergistic strategy for expansion of chemical space and the synthesis of valuable molecules (e.g. carbocycles and heterocycles), with up to three quaternary stereocenters, in a highly enantioselective fashion from simple alcohols (31examples, 95:5 to >99.5:0.5 e.r.) using integrated heterogeneous metal/chiral amine multiple relay catalysis and air/O-2 as the terminal oxidant. A novel highly 1,4-selective heterogeneous metal/amine co-catalyzed hydrogenation of enals was also added to the relay catalysis sequences.

  • 11.
    Engström, Karin
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Johnston, Eric V.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Verho, Oscar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Gustafson, Karl P. J.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Shakeri, Mozaffar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bäckvall, Jan-E.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Co-immobilization of an Enzyme and a Metal into the Compartments of Mesoporous Silica for Cooperative Tandem Catalysis: An Artificial Metalloenzyme2013Inngår i: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 52, nr 52, s. 14006-14010Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Surpassing nature: A hybrid catalyst in which Candida antarctica lipase B and a nanopalladium species are co-immobilized into the compartments of mesoporous silica is presented. The metal nanoparticles and the enzyme are in close proximity to one another in the cavities of the support. The catalyst mimics a metalloenzyme and was used for dynamic kinetic resolution of a primary amine in high yield and excellent enantioselectivity.

  • 12.
    Gebauer, Denis
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för materialkemi.
    Gunawidjaja, Philips N.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för fysikalisk kemi.
    Ko, J. Y. Peter
    Bacsik, Zoltan
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för materialkemi.
    Aziz, Baroz
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för materialkemi.
    Liu, Lijia
    Hu, Yongfeng
    Bergström, Lennart
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för materialkemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för oorganisk kemi och strukturkemi.
    Sham, Tsun-Kong
    Edén, Mattias
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för fysikalisk kemi.
    Hedin, Niklas
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för materialkemi.
    Proto-Calcite and Proto-Vaterite in Amorphous Calcium Carbonates2010Inngår i: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 49, nr 47, s. 8889-8891Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Amorphous order: Amorphous calcium carbonates (ACC) have an intrinsic structure relating to the crystalline polymorphs of calcite and vaterite. The proto-crystalline structures of calcite and vaterite (pc-ACC and pv-ACC) are analyzed by NMR (see picture), IR, and EXAFS spectroscopy, which shows that the structuring of ACC relates to the underlying pH-dependent equilibria.

  • 13.
    Gustafson, Karl P. J.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Görbe, Tamás
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    de Gonzalo Calvo, Gonzalo
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Yuan, Ning
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Schreiber, Cynthia
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Shchukarev, Andrey
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Persson, Ingmar
    Bäckvall, Jan-Erling
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Application and further structure elucidation of Pd(0)-CalB CLEA biohybrid catalyst- Chemoenzymatic dynamic kinetic resolution of primary benzylic aminesManuskript (preprint) (Annet vitenskapelig)
  • 14.
    Gustafson, Karl P. J.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Shatskiy, Andrey
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Verho, Oscar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Kärkäs, Markus D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Schluschass, Bastian
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Åkermark, Björn
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Bäckvall, Jan-Erling
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Johnston, Eric V.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Water oxidation mediated by ruthenium oxide nanoparticles supported on siliceous mesocellular foam2017Inngår i: Catalysis Science & Technology, ISSN 2044-4753, E-ISSN 2044-4761, Vol. 7, nr 1, s. 293-299Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Artificial photosynthesis is an attractive strategy for converting solar energy into fuel. In this context, development of catalysts for oxidation of water to molecular oxygen remains a critical bottleneck. Herein, we describe the preparation of a well-defined nanostructured RuO2 catalyst, which is able to carry out the oxidation of water both chemically and photochemically. The developed heterogeneous RuO2 nanocatalyst was found to be highly active, exceeding the performance of most known heterogeneous water oxidation catalysts when driven by chemical or photogenerated oxidants.

  • 15.
    Hallberg, Rolf
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för geologiska vetenskaper.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Multiwall Carbon Nanotubes and Nanofibers in Gallionella2014Inngår i: Geomicrobiology Journal, ISSN 0149-0451, E-ISSN 1521-0529, Vol. 31, nr 9, s. 764-768Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This is a report of microbial formation of multiwall carbon nanotubes (MWCNT) and nanofibers at normal pressure and temperature. Our results demonstrate a single cell organism's ability to form complicated material of high industrial interest. The microorganism, Gallionella, is classified as autotrophic and dysoxic. It uses CO2 for its carbon source and grows in environments with low concentrations of free oxygen. The organisms were taken from a deep bedrock tunnel where water leaking from cracks in the rock formed a precipitate of iron as a bacterial slime on the rock wall. Detailed investigations of the samples by transmission electron microscopy (TEM) revealed several types of MWCNT. The stalk single MWCNT was observed with a diameter of about 10nm and with an inner diameter of 1.35nm. The wall of the nanotube is built by graphite layers. The 10 to 20 sheets are used to form the tubes. The measured spacing between the lines is 0.34nm, which is an average value of interlayer spacing, close to the graphitic distance (0.335nm). HRTEM images reveal a two-dimensional lattice with a spacing of 0.24nm, indicating the presence of graphene.

  • 16. Hu, Guangzhi
    et al.
    Nitze, Florian
    Barzegar, Hamid Reza
    Sharifi, Tiva
    Mikolajczuk, Ania
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Borodzinski, Andrzej
    Wagberg, Thomas
    Palladium nanocrystals supported on helical carbon nanofibers for highly efficient electro-oxidation of formic acid, methanol and ethanol in alkaline electrolytes2012Inngår i: Journal of Power Sources, ISSN 0378-7753, E-ISSN 1873-2755, Vol. 209, s. 236-242Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We present the synthesis of palladium nanocrystals self-assembled on helical carbon nanofibers functionalized with benzyl mercaptan (Pd-S-HCNFs) and their electrocatalytic activity toward the oxidation of formic acid, methanol and ethanol. Helical carbon nanofibers (HCNFs) were first functionalized with benzyl mercaptan based on the pi-pi interactions between phenyl rings and the graphitic surface of HCNFs. Palladium nano crystals (PdNC) were fixed on the surface of functionalized HCNF by Pd-S bonds in a simple self-assembly method. The as-prepared materials were characterized by high resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), cyclic voltammetry (CV), and fuel cell tests. CV characterization of the as-prepared materials shows a very high electrocatalytic activity for oxidation of formic acid, ethanol and methanol in strong alkaline electrolyte. In comparison to commercial catalyst Vulcan XC-72 decorated with Pd nanoparticles, the proposed Pd-S-HCNFs nano composite material shows oxidation currents for formic acid, ethanol and methanol at the Pd-S-HCNF-modified electrode that are higher than that at the Pd/XC-72 modified electrode with a factor of 2.0, 1.5, and 2.3, respectively. In a formic acid fuel cell the Pd-S-HCNF modified electrode yields equal power density as commercial Pd/XC-72 catalyst. Our results show that Pd-decorated helical carbon nanofibers with diameters around 40-60 nm have very high potential as active material in fuel cells, electrocatalysts and sensors.

  • 17. Hu, Guangzhi
    et al.
    Sharifi, Tiva
    Nitze, Florian
    Barzegar, Hamid Reza
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Wagberg, Thomas
    Phase-transfer synthesis of amorphous palladium nanoparticle-functionalized 3D helical carbon nanofibers and its highly catalytic performance towards hydrazine oxidation2012Inngår i: Chemical Physics Letters, ISSN 0009-2614, E-ISSN 1873-4448, Vol. 543, s. 96-100Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Amorphous palladium nanoparticles functionalized helical carbon nanofibers (ApPd-HCNFs) were synthesized using a phase-transfer method. Palladium nanoparticles (Pd-NP) were first prepared using n-dodecyl sulfide as reducing agent and stabilizing ligands in ethanol. The Pd-NPs were then modified with benzyl mercaptan and transferred into a toluene solution with HCNFs which were decorated with amorphous palladium. The materials were characterized with high-resolution transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy and cyclic voltammetry showing that amorphous palladium nanoparticles were uniformly anchored at the HCNFs surface and that the ApPd-HCNFs exhibit high electrocatalytic activity towards hydrazine oxidation.

  • 18. Ibrahem, Ismail
    et al.
    Iqbal, Muhammad Naeem
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi. Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Verho, Oscar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Eivazihollagh, Alireza
    Olsén, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Edlund, Håkan
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Norgren, Magnus
    Johnston, Eric V.
    Copper Nanoparticles on Controlled Pore Glass and TEMPO for the Aerobic Oxidation of Alcohols2018Inngår i: ChemNanoMat, ISSN 2199-692X, Vol. 4, nr 1, s. 71-75Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Herein, we report on the facile synthesis of a heterogeneous copper nanocatalyst and its combination with 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) for the aerobic oxidation of alcohols to their corresponding carbonyl compounds. This low cost copper nanocatalyst was found to exhibit excellent recyclability, making it a highly attractive catalytic system from an economical and environmental point of view. Extensive characterization of the catalyst by a number of techniques revealed that it was comprised of well-dispersed Cu(I/II) nanoparticles with an average size of around 6nm.

  • 19. Jia, Xueen
    et al.
    Hu, Guangzhi
    Nitze, Florian
    Barzegar, Hamid Reza
    Sharifi, Tiva
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Wågberg, Thomas
    Synthesis of Palladium/Helical Carbon Nanofiber Hybrid Nanostructures and Their Application for Hydrogen Peroxide and Glucose Detection2013Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 5, nr 22, s. 12017-12022Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on a novel sensing platform for H2O2 and glucose based on immobilization of palladium-helical carbon nanofiber (Pd-HCNF) hybrid nanostnictures and glucose oxidase (GOx) with Nafion on a glassy carbon electrode (GCE). HCNFs were synthesized by a chemical vapor deposition process on a C-60-supported Pd catalyst. Pd-HCNF nanocomposites were prepared by a one-step reduction free method in dimethylformamide (DMF). The prepared materials were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Raman spectroscopy. The Nafion/Pd-HCNF/GCE sensor exhibits excellent electrocatalytic sensitivity toward H2O2 (315 mA M-1 cm(-2)) as probed by cyclic voltammetry (CV) and chronoamperometry. We show that Pd-HCNF-modified electrodes significantly reduce the overpotential and enhance the electron transfer rate. A linear range from 5.0 mu M to 2.1 mM with a detection limit of 3.0 mu M (based on the S/N = 3) and good reproducibility were obtained. Furthermore, a sensing platform for glucose was prepared by immobilizing the Pd-HCNFs and glucose oxidase (GOx) with Nafion on a glassy carbon electrode. The resulting biosensor exhibits a good response to glucose with a wide linear range (0.06-6.0 mM) with a detection limit of 0.03 mM and a sensitivity of 13 mA M-1 cm(-2). We show that small size and homogeneous distribution of the Pd nanoparticles in combination with good conductivity and large surface area of the HCNFs lead to a H2O2 and glucose sensing platform that performs in the top range of the herein reported sensor platforms.

  • 20.
    Johnston, Eric V.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Verho, Oscar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Kärkäs, Markus
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Shakeri, Mozaffar
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Palmgren, Pål
    Eriksson, Kristofer
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Oscarsson, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Bäckvall, Jan-E.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Highly dispersed palladium nanoparticles on mesocellular foam: an efficient and recyclable heterogeneous catalyst for alcohol oxidation2012Inngår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 18, nr 39, s. 12202-12206Artikkel i tidsskrift (Fagfellevurdert)
  • 21. Kumar, Ankit
    et al.
    Wetterskog, Erik
    Lewin, Erik
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Akansel, Serkan
    Husain, Sajid
    Edvinsson, Tomas
    Brucas, Rimantas
    Chaudhary, Sujeet
    Svedlindh, Peter
    Effect of in situ electric-field-assisted growth on antiphase boundaries in epitaxial Fe3O4 thin films on MgO2018Inngår i: Physical review materials, ISSN 2475-9953, Vol. 2, nr 5, artikkel-id 054407Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Antiphase boundaries (APBs) normally form as a consequence of the initial growth conditions in all spinel ferrite thin films. These boundaries result from the intrinsic nucleation and growth mechanism, and are observed as regions where the periodicity of the crystalline lattice is disrupted. The presence of APBs in epitaxial films of the inverse spinel Fe3O4 alters their electronic and magnetic properties due to strong antiferromagnetic (AF) interactions across these boundaries. We explore the effect of using in-plane in situ electric-field-assisted growth on the formation of APBs in heteroepitaxial Fe3O4(100)/MgO(100) thin films. The electric-field-assisted growth is found to reduce the AF interactions across APBs and, as a consequence, APB-free thin-film-like properties are obtained, which have been probed by electronic, magnetic, and structural characterization. The electric field plays a critical role in controlling the density of APBs during the nucleation process by providing an electrostatic force acting on adatoms and therefore changing their kinetics. This innovative technique can be employed to grow epitaxial spinel thin films with controlled AF interactions across APBs.

  • 22.
    Lee, Kian Keat
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Hao, Wenming
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Gustafsson, Mikaela
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Morin, Daniel
    Björkman, Eva
    Lilliestråle, Malte
    Björefors, Fredrik
    Andersson, Anna M.
    Hedin, Niklas
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tailored activated carbons for supercapacitors derived from hydrothermally carbonized sugars by chemical activation2016Inngår i: RSC Advances, ISSN 2046-2069, E-ISSN 2046-2069, Vol. 6, nr 112, s. 110629-110641Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Activated carbons (ACs) are actively researched as electrode materials for supercapacitors and there is a significant interest to produce ACs from sustainable and low cost precursors. In this study, various ACs were prepared from hydrothermally carbonized sugars by KOH activation. Both the hydrothermal carbonization and activation processes were optimized to tailor the properties (e.g. textural properties, chemical composition, N-doping, electrical conductivity) of the ACs. For instance, the Brunauer-Emmett-Teller (BET) surface areas (S-BET) were tuned in the range of 800-3000 m(2) g(-1) with associated variation in the extent of microporosity and pore size distributions (PSDs). The ACs were evaluated electrochemically as materials for supercapacitor electrodes in a symmetrical two-electrode cell using an aqueous electrolyte. The relationship between the electrochemical, textural, electrical, and physicochemical properties were analyzed systematically to understand the key factors determining the electrochemical performance. A high specific capacitance (C-m) of similar to 260 F g(-1) was achieved at a moderately high S-BET of similar to 1300 m(2) g(-1), which was equivalent to a C-m/S-BET of 20 mu F cm(-2), for an optimal AC prepared from hydrothermally carbonized glucose. The very high surface-specific capacitance highlights that the specific surface area is certainly not the sole limiting parameter for effective electrode materials.

  • 23. Liu, Chenjuan
    et al.
    Younesi, Reza
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Valvo, Mario
    Edström, Kristina
    Gustafsson, Torbjörn
    Zhu, Jiefang
    3-D binder-free graphene foam as a cathode for high capacity Li-O-2 batteries2016Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 4, nr 25, s. 9767-9773Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    To provide energy densities higher than those of conventional Li-ion batteries, a Li-O-2 battery requires a cathode with high surface area to host large amounts of discharge product Li2O2. Therefore, reversible formation of discharge products needs to be investigated in Li-O-2 cells containing high surface area cathodes. In this study, a binder-free oxygen electrode consisting of a 3-D graphene structure on aluminum foam, with a high defect level (I-D/I-G = 1.38), was directly used as the oxygen electrode in LiO2 batteries, delivering a high capacity of about 9 x 10(4) mA h g(-1) (based on the weight of graphene) at the first full discharge using a current density of 100 mA g(graphene)(-1). This performance is attributed to the 3-D porous structure of graphene foam providing both an abundance of available space for the deposition of discharge products and a high density of reactive sites for Li-O-2 reactions. Furthermore, the formation of discharge products with different morphologies and their decomposition upon charge were observed by SEM. Some nanoscaled LiOH particles embedded in the toroidal Li2O2 were detected by XRD and visualized by TEM. The amount of Li2O2 formed at the end of discharge was revealed by a titration method combined with UV-Vis spectroscopy analysis.

  • 24. Ma, Yue
    et al.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Gustafsson, Torbjörn
    Edström, Kristina
    Recycled Poly(vinyl alcohol) Sponge for Carbon Encapsulation of Size-Tunable Tin Dioxide Nanocrystalline Composites2015Inngår i: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 8, nr 12, s. 2084-2092Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The recycling of industrial materials could reduce their environmental impact and waste haulage fees and result in sustainable manufacturing. In this work, commercial poly(vinyl alcohol) (PVA) sponges are recycled into a macroporous carbon matrix to encapsulate size-tunable SnO2 nanocrystals as anode materials for lithium-ion batteries (LIBs) through a scalable, flash-combustion method. The hydroxyl groups present copiously in the recycled PVA sponges guarantee a uniform chemical coupling with a tin(IV) citrate complex through intermolecular hydrogen bonds. Then, a scalable, ultrafast combustion process (30s) carbonizes the PVA sponge into a 3D carbon matrix. This PVA-sponge-derived carbon could not only buffer the volume fluctuations upon the Li-Sn alloying and dealloying processes but also afford a mixed conductive network, that is, a continuous carbon framework for electrical transport and macropores for facile electrolyte percolation. The best-performing electrode based on this composite delivers a rate performance up to 9.72C (4Ag(-1)) and long-term cyclability (500cycles) for Li+ ion storage. Moreover, cyclic voltammograms demonstrate the coexistence of alloying and dealloying processes and non-diffusion-controlled pseudocapacitive behavior, which collectively contribute to the high-rate Li+ ion storage.

  • 25. Ma, Yue
    et al.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Li, Shaowen
    Edström, Kristina
    Wei, Bingqing
    Multiscale Interfacial Strategy to Engineer Mixed Metal-Oxide Anodes toward Enhanced Cycling Efficiency2018Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 10, nr 23, s. 20095-20105Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Interconnected macro/mesoporous structures of mixed metal oxide (MMO) are developed on nickel foam as freestanding anodes for Li-ion batteries. The sustainable production is realized via a wet chemical etching process with bio-friendly chemicals. By means of divalent iron doping during an in situ recrystallization process, the as-developed MMO anodes exhibit enhanced levels of cycling efficiency. Furthermore, this atomic-scale modification coherently synergizes with the encapsulation layer across a micrometer scale. During this step, we develop a quasi-gel-state tri-copolymer, i.e., F127-resorcinol-melamine, as the N-doped carbon source to regulate the interfacial chemistry of the MMO electrodes. Electrochemical tests of the modified FexN1-xO@NC-NiF anode in both half-cell and full-cell configurations unravel the favorable suppression of the irreversible capacity loss and satisfactory cyclability at the high rates. This study highlights a proof-of-concept modification strategy across multiple scales to govern the interfacial chemical process of the electrodes toward better reversibility.

  • 26. Ma, Yue
    et al.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Younesi, Reza
    Gustafsson, Torbjörn
    Lee, Jim Yang
    Edström, Kristina
    Iron Doping in Spinel NiMn2O4: Stabilization of the Mesoporous Cubic Phase and Kinetics Activation toward Highly Reversible Li+ Storage2015Inngår i: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 27, nr 22, s. 7698-7709Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Quaternary oxide structures with a three-dimensional macro/mesoporous network are synthesized via a facile nanocasting method followed by a calcination process. Structural engineering integrates multiscale pores by using a hydrophilic membrane with tunable-porosity as the sacrificial template. Through tailoring the metal precursor ratio, the tetragonal sites of spinel oxide are preferentially occupied by iron, resulting in a stabilized mesoporous cubic phase. Crystal field theory together with compositional characterizations from energy-dispersive spectrometry (EDS), X-ray photoelectron spectroscopy (XPS), Mossbauer, and electron energy loss spectroscopy (EELS) direct our detailed analysis of the cation distribution in the spinel structures. Galvanostatic tests based on the best performing electrode exhibits a robust cycle life stable for 1200 cycles at a high current density of 1500 mA g(-1). This good Li+ storage performance could be attributed to the mutually beneficial synergy of the optimal level of iron doping which improves the electrical conductivity and structural robustness, as well as the presence of extended, hierarchical macro/mesoporous network. Finally, we demonstrate three feasible surface modification strategies for the oxide anodes toward better reversibility of Li+ storage.

  • 27.
    Malmgren, Joel
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Nagendiran, Anuja
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bäckvall, Jan-Erling
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Olofsson, Berit
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    C-2 Selective Arylation of Indoles with Heterogeneous Nanopalladium and Diaryliodonium Salts2014Inngår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 20, nr 42, s. 13531-13535Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A simple and efficient method to prepare synthetically useful 2-arylindoles is presented, using a heterogeneous Pd catalyst and diaryliodonium salts in water under mild conditions. A remarkably low leaching of metal catalyst was observed under the applied conditions. The developed protocol is highly C-2 selective and tolerates structural variations both in the indole and in the diaryliodonium salt. Arylations of both NH indoles and N-protected indoles with ortho-substituted, electron-rich, electron-deficient, or halogenated diaryliodonium salts were achieved to give the desired products in high to excellent isolated yields within 6 to 15 h at room temperature or 40 °C.

  • 28.
    Mayence, Arnaud
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Wery, Madeleine
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Wetterskog, Erik
    Svedlindh, Peter
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bergström, Lennart
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Interfacial strain and defects in asymmetric Fe-Mn oxide hybrid nanoparticles2016Inngår i: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 8, nr 29, s. 14171-14177Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Asymmetric Fe-Mn oxide hybrid nanoparticles have been obtained by a seed-mediated thermal decomposition-based synthesis route. The use of benzyl ether as the solvent was found to promote the orientational growth of Mn1-xO onto the iron oxide nanocube seeds yielding mainly dimers and trimers whereas 1-octadecene yields large nanoparticles. HRTEM imaging and HAADF-STEM tomography performed on dimers show that the growth of Mn1-xO occurs preferentially along the edges of iron oxide nanocubes where both oxides share a common crystallographic orientation. Fourier filtering and geometric phase analysis of dimers reveal a lattice mismatch of 5% and a large interfacial strain together with a significant concentration of defects. The saturation magnetization is lower and the coercivity is higher for the Fe-Mn oxide hybrid nanoparticles compared to the iron oxide nanocube seeds.

  • 29.
    Nagendiran, Anuja
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Sörensen, Henrik
    Johansson, Magnus J.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bäckvall, Jan-E.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
    Nanopalladium-catalyzed conjugate reduction of Michael acceptors - application in flow2016Inngår i: Green Chemistry, ISSN 1463-9262, E-ISSN 1463-9270, Vol. 18, nr 9, s. 2632-2637Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A continuous-flow approach towards the selective nanopalladium-catalyzed hydrogenation of the olefinic bond in various Michael acceptors, which could lead to a greener and more sustainable process, has been developed. The nanopalladium is supported on aminofunctionalized mesocellular foam. Both aromatic and aliphatic substrates, covering a variation of functional groups such as acids, aldehydes, esters, ketones, and nitriles were selectively hydrogenated in high to excellent yields using two different flow-devices (H-Cube (R) and Vapourtec). The catalyst was able to hydrogenate cinnamaldehyde continuously for 24 h (in total hydrogenating 19 g cinnanmaldehyde using 70 mg of catalyst in the H-cube (R)) without showing any significant decrease in activity or selectivity. Furthermore, the metal leaching of the catalyst was found to be very low (ppb amounts) in the two flow devices.

  • 30.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    A TEM study of Bi0.5Na0.5TiO3-based ceramics2014Inngår i: 18th International Microscopy Congress, 2014Konferansepaper (Annet vitenskapelig)
  • 31.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Diffuse electron scattering in Bi0.5Na0.5TiO3-based ceramics2014Inngår i: Electroceramics XIV, 2014Konferansepaper (Annet vitenskapelig)
  • 32.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Investigation of local structural phase transitions in 95Na0.5Bi0.5TiO3-5BaTiO3 piezoceramics by mean of in-situ transmission electron microscopyManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The temperature-dependence of superstructure reflections, diffuse scattering intensity and ferroelectric domains morphology for 95Na0.5Bi0.5TiO3-5BaTiO3 ceramic was investigated by in-situ transmission electron microscopy. A subtle local structural phase transition was observed around 110°C. This local phase transition is characterized by a transformation in the dominant octahedral-tilt system from antiphase to in-phase tilting and was correlated with the depolarization mechanism common in this type of materials. Simulations of octahedral-tilt disorder were developed at different temperatures which enabled us to provide a comprehensive structural model that explains the temperature-dependence of superstructure reflections and electron diffuse scattering intensity. This model revealed that plate-like in-phase nanodomains tilted about three orthogonal axes coexist with an antiphase tilted matrix, even at room temperature. With increasing temperature, the concentration of in-phase nanodomains is increased till a critical volume fraction is reached. We propose that these plate-like in-phase nanodomains are an inherent characteristic of NBT-based compounds and that the local phase transition observed around 110°C leads to a disruption in the long-range ferroelectric order and is responsible for the depolarization mechanism.

  • 33.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Investigation of local structural phase transitions in 95Na(0.5)Bi(0.5)TiO(3)-5BaTiO(3) piezoceramics by means of in-situ transmission electron microscopy2018Inngår i: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 123, nr 24, artikkel-id 244105Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The temperature-dependence of superstructure reflections, diffuse scattering intensity, and ferroelectric domain morphology for 95Na(0.5)Bi(0.5)TiO(3)-5BaTiO(3) ceramics was investigated by in-situ transmission electron microscopy. A subtle local structural phase transition was observed around 110 degrees C. This local phase transition is characterized by a transformation in the dominant octahedral-tilt system from antiphase to in-phase tilting and was correlated with the depolarization mechanism common in this type of materials. Simulations of the octahedral-tilt disorder were developed at different temperatures which enabled us to provide a comprehensive structural model that explains the temperature-dependence of superstructure reflections and electron diffuse scattering intensity. This model revealed that plate-like in-phase nanodomains tilted about three orthogonal axes coexist with an antiphase tilted matrix, even at room temperature. With increasing temperature, the concentration of in-phase nanodomains is increased till a critical volume fraction is reached. We propose that these plate-like in-phase nanodomains are an inherent characteristic of NBT-based compounds and that the local phase transition observed around 110 degrees C leads to a disruption in the long-range ferroelectric order and is responsible for the depolarization mechanism.

  • 34.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Local disorder in Na0.5Bi0.5TiO3-piezoceramic determined by 3D electron diffuse scattering2017Inngår i: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 7, artikkel-id 12519Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Local structural distortions in Na0.5Bi0.5TiO3-based solid solutions have been proved to play a crucial role in understanding and tuning their enhanced piezoelectric properties near the morphotropic phase boundary. In this work all local structural disorders in a lead-free ternary system, namely 85% Na0.5Bi0.5TiO3-10% Bi0.5K0.5TiO3-5% BaTiO3, were mapped in reciprocal space by 3D electron diffraction. Furthermore, a comprehensive model of the local disorder was developed by analysing the intensity and morphology of the observed weak diffuse scattering. We found that the studied ceramics consists of plate-like in-phase oxygen octahedral nanoscale domains randomly distributed in an antiphase tilted matrix. In addition, A-site chemical short-range order of Na/Bi and polar displacements contribute to different kinds of diffuse scattering. The proposed model explains all the observed diffraction features and offers insight into the ongoing controversy over the nature of local structural distortions in Na0.5Bi0.5TiO3-based solid solutions.

  • 35.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Study of local ordering in lead-free ferroelectrics2014Konferansepaper (Annet vitenskapelig)
  • 36.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Study of local structural disorder in 0.6PbIn½Nb½O3-0.4PbMgNbO3 ceramics as revealed by 3D electron diffuse scatteringManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    The local structural disorder in 0.6PbIn½Nb½O3-0.4PbMgNbO3 ceramic was revealed by 3D electron diffraction. Rotation electron diffraction method was applied to reconstruct the 3D reciprocal space volume containing both diffuse scattering and Bragg reflections. The butterfly-shaped diffuse scattering in the vicinity of h00 type reflections and the ellipsoidal-shaped diffuse scattering in the vicinity of hk0 type reflections were detected. Moreover, sharp superstructure reflections and strong diffuse scattering sheets along <110>* directions were observed in thin-volume sections centered along several zone axes cut from the 3D reciprocal space volume. This indicates that the local structure deviates significantly from the average one. By analyzing the intensity and morphology of diffraction features in 3D a model of structural disorder was developed comprising of 1:1 chemical short-range order of B-site cations and local displacements of Pb atoms. The final local structure is more akin to a spin glass state and no polar nanoregions were observed. This model was able to explain all significant diffraction features observed in volume-sections centered along three different zone axes.

  • 37.
    Neagu, Alexandra
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    The influence of potassium content on octahedral-tilt disorder in Na0.5Bi0.5TiO3-solid solutions near morphotropic phase boundary2018Inngår i: Scripta Materialia, ISSN 1359-6462, E-ISSN 1872-8456, Vol. 152, s. 49-54Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A semi-quantitative comparison of 3D electron diffraction data revealed structural differences at the nanoscale for three (95-x)Na0.5Bi0.5TiO3-xK0.5Bi0.5TiO3-5BaTiO3 solid solutions close to the morphotropic phase boundary, with x = 0, 5, 10. Using a novel rotation electron diffraction technique, diffuse scattering intensity was recorded in 3D as continuous rods along hk0.5 reciprocal-planes. By analyzing the different superstructure reflections and the intensity/morphology of diffuse scattering, a structural model of the local octahedral-tilt disorder for the different ceramics was developed. A good agreement was obtained between the experimental and simulated data with a model comprising of antiphase (aaa) and plate-like in-phase (a0a0c+) nanodomains.

  • 38.
    Nedumkandathil, Reji
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Jaworski, Aleksander
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Grins, Jekabs
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bernin, Diana
    Karlsson, Maths
    Eklof-Österberg, Carin
    Neagu, Alexandra
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Pell, Andrew J.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Häussermann, Ulrich
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Hydride Reduction of BaTiO3 - Oxyhydride Versus O Vacancy Formation2018Inngår i: Acs Omega, ISSN 2470-1343, Vol. 3, nr 9, s. 11426-11438Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We investigated the hydride reduction of tetragonal BaTiO3 using the metal hydrides CaH2, NaH, MgH2, NaBH4, and NaAlH4. The reactions employed molar BaTiO3/H ratios of up to 1.8 and temperatures near 600 degrees C. The air-stable reduced products were characterized by powder X-ray diffraction (PXRD), transmission electron microscopy, thermogravimetric analysis (TGA), and H-1 magic angle spinning (MAS) NMR spectroscopy. PXRD showed the formation of cubic products-indicative of the formation of BaTiO3-xHx. except for NaH. Lattice parameters were in a range between 4.005 angstrom (for NaBH4-reduced samples) and 4.033 A (for MgH2-reduced samples). With increasing H/BaTiO3 ratio, CaH2-, NaAlH4-, and MgH2-reduced samples were afforded as two-phase mixtures. TGA in air flow showed significant weight increases of up to 3.5% for reduced BaTiO3, suggesting that metal hydride reduction yielded oxyhydrides BaTiO3-xHx with x values larger than 0.5. H-1 MAS NMR spectroscopy, however, revealed rather low concentrations of H and thus a simultaneous presence of O vacancies in reduced BaTiO3. It has to be concluded that hydride reduction of BaTiO3 yields complex disordered materials BaTiO3-xHy square((x-y)) with x up to 0.6 and y in a range 0.04-0.25, rather than homogeneous solid solutions BaTiO3-xHx. Resonances of (hydridic) H substituting O in the cubic perovskite structure appear in the -2 to -60 ppm spectral region. The large range of negative chemical shifts and breadth of the signals signifies metallic conductivity and structural disorder in BaTiO3-xHy square((x-y)). Sintering of BaTiO3-xHy square((x-y)) in a gaseous H-2 atmosphere resulted in more ordered materials, as indicated by considerably sharper H-1 resonances.

  • 39.
    Nedumkandathil, Reji
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Jaworski, Aleksander
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Grins, Jekabs
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Bernin, Diana
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Karlsson, Maths
    Österberg, Carin
    Neagu, Alexandra
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Pell, Andrew J.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Häussermann, Ulrich
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Hydride Reduction of BaTiO3 – Oxyhydride vs O-Vacancy FormationManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    We investigated the hydride reduction of tetragonal BaTiO3 using the metal hydrides CaH2, NaH, MgH2, NaBH4 and NaAlH4. The reactions employed molar BaTiO3:H ratios of up to 1.8 and temperatures near 600 °C. The air stable reduced products were characterized by powder X-ray diffraction (PXRD), transmission electron microscopy, thermogravimetric analysis (TGA) and solid-state 1H NMR spectroscopy. PXRD showed the formation of cubic products - indicative of the formation of BaTiO3-xHx - except for NaH. Lattice parameters were in a range between 4.005 Å (for NaBH4 reduces samples) and 4.033 Å (for MgH2 reduced samples). With increasing BaTiO3:H ratio, CaH2, NaAlH4 and MgH2 reduced samples were afforded as two-phase mixtures. TGA in air flow showed significant weight increase of up to 3.5 % for reduced BaTiO3, suggesting that metal hydride reduction yielded oxyhydrides BaTiO3-xHx with x values larger 0.5. 1H NMR, however, revealed rather low concentrations of H, and, thus a simultaneous presence of O vacancies in reduced BaTiO3. It has to be concluded that hydride reduction of BaTiO3 yields complex disordered materials BaTiO3-xHy(x-y) with x up to 0.6, y in a range 0.05 – 0.2 and (x-y) > y, rather than homogeneous solid solutions BaTiO3Hx. Resonances of (hydridic) H substituting O in the cubic perovskite structure appear in the -2 to -60 ppm spectral region. The large range of chemical shifts and breadth of the signals signifies the structural disorder in BaTiO3-xHy(x-y). Sintering of BaTiO3-xHy(x-y) in a gaseous H2 atmosphere resulted in more ordered materials as indicated by considerably sharper 1H resonances.

  • 40.
    Nitze, Florian
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för oorganisk kemi och strukturkemi.
    Hu, Guangzhi
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för oorganisk kemi och strukturkemi.
    Wågberg, Thomas
    Synthesis and characterization of palladium carbon nanostructure composites2011Konferansepaper (Annet vitenskapelig)
    Abstract [en]

    We present a synthesis approach to produce carbon nanostructures decorated with Pd nanoparticles. Helical carbon nanofibers were synthesized by CVD on Pd supported C 60 catalyst. Their structure has a high and unique surface area. They are an ideal candidate to be decorated with metallic nanoparticles. Nanostructures were functionalized by H 2O2, HNO3 or benzyl mercaptan. The attached functional groups improved the hydrophilicity of the surface and created attachment sites for Pd. Carbon nanotubes and helical carbon nanofibers were successfully decorated with Pd nanoparticles. Transmission electron micrographs clearly show the successful decoration of the carbon support. The influence of the support was investigated. The material was also characterized by a variety of methods such as selected area electron diffraction and thermo gravimetric analysis. The composites show highcatalytic activity towards formic acid, methanol and ethanol oxidation investigated by cyclic voltammetry.

  • 41. Nitze, Florian
    et al.
    Mazurkiewicz, Marta
    Malolepszy, Artur
    Mikolajczuk, Anna
    Kedzierzawski, Piotr
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Hu, Guangzhi
    Kurzydlowski, Krzysztof Jan
    Stobinski, Leszek
    Borodzinski, Andrzej
    Wagberg, Thomas
    Synthesis of palladium nanoparticles decorated helical carbon nanofiber as highly active anodic catalyst for direct formic acid fuel cells2012Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 63, s. 323-328Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We present a single metal approach to produce highly active catalyst materials based on Pd-decorated helical carbon nanofibers. Helical carbon fibers are synthesized by a chemical vapor deposition process on a C-60 supported Pd catalyst and the obtained fibers are functionalized by H2O2 followed by a decoration with Pd nanoparticles. Although transmission electron microscopy images show that the decoration is relatively inhomogeneous the electrocatalytic activity for formic acid oxidation is very high. Cyclic voltammetry measurements (CV) show that the generated current peak value for Pd-decorated helical carbon nanofibers is 300 mA/mg(Pd) for a scan rate of 10 mV/s. This is significantly higher than the corresponding value of a reference sample of multiwalled carbon nanotubes decorated with Pd nanoparticles by the same process. Fuel cell tests for our Pd-decorated helical carbon nanofibers also displayed a high power density, although not as superior to Pd-decorated multiwalled nanotubes as measured by CV. Our results show that helical carbon nanofibers have several good properties, such as a rigid anchoring of catalyst nanoparticles and a suitable structure for creating functionalization defects which make them an interesting candidate for electrochemical applications. 

  • 42. Oltean, Gabriel
    et al.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Edström, Kristina
    Nyholm, Leif
    On the origin of the capacity fading for aluminium negative electrodes in Li-ion batteries2014Inngår i: Journal of Power Sources, ISSN 0378-7753, E-ISSN 1873-2755, Vol. 269, s. 266-273Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The origin of the capacity loss for aluminium negative electrodes in Li-ion batteries has been studied for electrodeposited aluminium nanorod electrodes coated with Al2O3 layers of different thicknesses (i.e. a native oxide layer, 30 and 60 nm) mainly employing pouch cell voltammetric cycling versus metallic lithium. Whereas the capacity decreased continuously during cycling between 0.1 and 3 V vs. Li+/Li, good cycling stability was obtained when the cycling was carried out between 0.1 and 1 V vs. Li+/Li. Since no significant dependence of the cycling stability on the thickness of the alumina layer was found in any of the experiments, the observed loss of capacity is unlikely to have been caused by volume expansion effects. The latter is further supported by the finding that the capacity (obtained when cycling between 0.1 and 3 V vs. Li+/Li) decreased linearly with the inverse of the square root of the cycling time, indicating that the capacity loss was due to the loss of lithium as a result of lithium diffusion into the bulk of the aluminium electrodes. The latter is explained based on a lithium-aluminium alloying and dealloying model which complements previously published models.

  • 43. Palo-Nieto, Carlos
    et al.
    Afewerki, Samson
    Anderson, Mattias
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Berglund, Per
    Córdova, Armando
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK). Mid Sweden University, Sweden.
    Integrated Heterogeneous Metal/Enzymatic Multiple Relay Catalysis for Eco-Friendly and Asymmetric Synthesis2016Inngår i: ACS Catalysis, ISSN 2155-5435, E-ISSN 2155-5435, Vol. 6, nr 6, s. 3932-3940Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Organic synthesis is in general performed using stepwise transformations where isolation and purification of key intermediates is often required prior to further reactions. Herein we disclose the concept of integrated heterogeneous metal/enzymatic multiple relay catalysis for eco-friendly and asymmetric synthesis of valuable molecules (e.g., amines and amides) in one-pot using a combination of heterogeneous metal and enzyme catalysts. Here reagents, catalysts, and different conditions can be introduced throughout the one-pot procedure involving multistep catalytic tandem operations. Several novel cocatalytic relay sequences (reductive amination/amidation, aerobic oxidation/reductive amination/amidation, reductive amination/kinetic resolution and reductive amination/ dynamic kinetic resolution) were developed. They were next applied to the direct synthesis of various biologically and optically active amines or amides in one-pot from simple aldehydes, ketones, or alcohols, respectively.

  • 44. Polido Legaria, Elizabeth
    et al.
    Rocha, Joao
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Kessler, Vadim G.
    Seisenbaeva, Gulaim A.
    Unusual seeding mechanism for enhanced performance in solid-phase magnetic extraction of Rare Earth Elements2017Inngår i: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 7, artikkel-id 43740Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Due to the increasing demand of Rare Earth Elements (REE or RE), new and more efficient techniques for their extraction are necessary, suitable for both mining and recycling processes. Current techniques such as solvent extraction or solid adsorbents entail drawbacks such as using big volumes of harmful solvents or limited capacity. Hybrid nanoadsorbents based on SiO2 and highly stable gamma-Fe2O3-SiO2 nanoparticles, proved recently to be very attractive for adsorption of REE, yet not being the absolute key to solve the problem. In the present work, we introduce a highly appealing new approach in which the nanoparticles, rather than behaving as adsorbent materials, perform as inducers of crystallization for the REE in the form of hydroxides, allowing their facile and practically total removal from solution. This induced crystallization is achieved by tuning the pH, offering an uptake efficiency more than 20 times higher than previously reported (up to 900 mg RE3+/g vs. 40 mg RE3+/g). The obtained phases were characterized by SEM-EDS, TEM, STEM and EFTEM and C-13 and Si-29 solid state NMR. Magnetic studies showed that the materials possessed enough magnetic properties to be easily removed by a magnet, opening ways for an efficient and industrially applicable separation technique.

  • 45. Qi, Kezhen
    et al.
    Selvaraj, Rengaraj
    Al Fahdi, Tharaya
    Al-Kindy, Salma
    Kim, Younghun
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Sillanpää, Mika
    Hierarchical alpha-MnS microspheres: Solvothermal synthesis and growth mechanism2016Inngår i: Materials letters (General ed.), ISSN 0167-577X, E-ISSN 1873-4979, Vol. 166, s. 116-120Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Hierarchical-like alpha-MnS microspheres have been successfully synthesized via a simple solvothermal route using L-Cystein as both sulfur source and capping agent. X-ray diffraction (XRD) analysis confirmed that these hierarchical microspheres were made of alpha-phase MnS. Morphological studies performed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) methods showed that the alpha-MnS hierarchical microspheres are obtained from the nanocubes by self-assembly due to the main driving force of the minimization of overall surface energy. It is highly expected this research can provide a useful fundamental understanding of shape-controlled synthesis of the semiconductor material with hierarchical microstructures.

  • 46. Qi, Kezhen
    et al.
    Selvaraj, Rengaraj
    Al Fahdi, Tharaya
    Al-Kindy, Salma
    Kim, Younghun
    Wang, Gui-Chang
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Sillanpää, Mika
    Enhanced photocatalytic activity of anatase-TiO2 nanoparticles by fullerene modification: A theoretical and experimental study2016Inngår i: Applied Surface Science, ISSN 0169-4332, E-ISSN 1873-5584, Vol. 387, s. 750-758Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A series of fullerene (C-60)-modified anatase TiO2 (a-TiO2) nanocomposites with different weight loadings of C-60 were successfully synthesized by a simple solution phase method. The as-prepared C-60@a-TiO2 nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, Brunauer-Emmett-Teller (BET), UV-vis diffuse reflectance absorption spectra (DRS), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and electron energy loss spectroscopy (EELS). The photocatalytic degradation of methylene blue (MB) by the neat a-TiO2 and C-60@a-TiO2 nanocomposites was investigated under UV-A light irradiation, demonstrating that C-60 effectively enhances the photocatalytic activity of a-TiO2 nanoparticles with an optimal amount of 2.0 wt%. By combining with the density functional theory (DFT) calculations, we investigated the electronic structures of C-60@a-TiO2 hetero-interfaces to reveal the underlying principle of the C-60 loading on the photocatalytic activity. It was found that the incorporation of C-60 on the a-TiO2 surface not only narrowed the band gap, but also introduced an additional doping state between the valance and conduction band. Therefore, the presence of intermediate electronic state will in turn contribute to the efficient charge separation and enhanced light adsorption for the C-60@a-TiO2 nanocomposites, resulting in an improved photocatalytic performance.

  • 47.
    Qi, Kezhen
    et al.
    Shenyang Normal University, Shenyang, China.
    Selvaraj, Rengaraj
    Sultan Qaboos University, Muscat, Sultanate of Oman.
    Jeong, Uiseok
    Kwangwoon University, Korea .
    Al-Kindy, Salma M. Z.
    Sultan Qaboos University, Muscat, Sultanate of Oman.
    Sillanpää, Mika
    Lappeenranta University of Technology, FInland.
    Kim, Younghun
    Kwangwoon University, Korea.
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Hierarchical-like multipod γ-MnS microcrystals: solvothermal synthesis, characterization and growth mechanism2015Inngår i: RSC Advances, ISSN 2046-2069, E-ISSN 2046-2069, Vol. 5, nr 13, s. 9618-9620Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Novel hierarchical multipod gamma-MnS microcrystals have been successfully synthesized by a simple solvothermal method, in which manganese acetate was used as a manganese source and thiosemicarbazide was used as both sulfur source and capping agent.

  • 48. Raudonyte-Svirbutaviciene, Eva
    et al.
    Neagu, Alexandra
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Vickackaite, Vida
    Jasulaitiene, Vitalija
    Zarkov, Aleksej
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Katelnikovas, Arturas
    Two-step photochemical inorganic approach to the synthesis of Ag-CeO2 nanoheterostructures and their photocatalytic activity on tributyltin degradation2018Inngår i: Journal of Photochemistry and Photobiology A: Chemistry, ISSN 1010-6030, E-ISSN 1873-2666, Vol. 351, s. 29-41Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Herein, we report a simple, sustainable and low-cost approach to design Ag-CeO2 nanoheterostructures in pure aqueous and ethanol containing aqueous solutions via photochemical UV-light driven process with no capping agents nor stabilizers required. To this end, photochemically synthesized CeO2 nanoparticles were applied as photoactive compounds in order to generate formation of metallic silver nanoparticles. Irradiation of deaerated CeO2 suspensions in the presence of Ag+ resulted in the rise of a strong surface plasmon resonance band with a maximum at 393-422 nm in the absorption spectra of the solutions, indicating formation of small metallic silver particles. Faster formation of Ag nanoparticles with the lower amount of silver precursor being required was observed when ethanol was introduced to the reaction solution before the irradiation. This implies that oxidative reactions can be strongly suppressed in deaerated ethanol containing solutions with respect to the pure aqueous media. Not only was the overall efficiency of the process remarkably increased by the use of alcohol, but also smaller and more uniform silver nanoparticles with a size comparable to that of ceria nanoparticles (around 15 nm) were formed when compared to those synthesized without radical scavengers as revealed by TEM analysis. The proposed photochemical approach enables the production of silver-semiconductor system without employing organic stabilizers, thus resulting in formation of nanoparticles with clean, highly reactive metal surface. The as-synthesized silver-ceria nanoheterostructures demonstrated enhanced visible light driven photocatalytic activity on tributyltin (TBT) degradation if compared to pure ceria nanoparticles.

  • 49. Rehnlund, David
    et al.
    Valvo, Mario
    Tai, Cheuk-Wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Ångström, Jonas
    Sahlberg, Martin
    Edström, Kristina
    Nyholm, Leif
    Electrochemical fabrication and characterization of Cu/Cu2O multi-layered micro and nanorods in Li-ion batteries2015Inngår i: Nanoscale, ISSN 2040-3364, E-ISSN 2040-3372, Vol. 7, nr 32, s. 13591-13604Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Electrodes composed of freestanding nano- and microrods composed of stacked layers of copper and cuprous oxide have been fabricated using a straightforward one-step template-assisted pulsed galvanostatic electrodeposition approach. The approach provided precise control of the thickness of each individual layer of the high-aspect-ratio rods as was verified by SEM, EDS, XRD, TEM and EELS measurements. Rods with diameters of 80, 200 and 1000 nm were deposited and the influence of the template pore size on the structure and electrochemical performance of the conversion reaction based electrodes in lithium-ion batteries was investigated. The multi-layered Cu2O/Cu nano-and microrod electrodes exhibited a potential window of more than 2 V, which was ascribed to the presence of a distribution of Cu2O (and Cu, respectively) nanoparticles with different sizes and redox potentials. As approximately the same areal capacity was obtained independent of the diameter of the multi-layered rods the results demonstrate the presence of an electroactive Cu2O layer with a thickness defined by the time domain of the measurements. It is also demonstrated that while the areal capacity of the electrodes decreased dramatically when the scan rate was increased from 0.1 to 2 mV s(-1), the capacity remained practically constant when the scan rate was further increased to 100 mV s(-1). This behaviour can be explained by assuming that the capacity is limited by the lithium ion diffusion rate though the Cu2O layer generated during the oxidation step. The electrochemical performance of present type of 3-D multi-layered rods provides new insights into the lithiation and delithiation reactions taking place for conversion reaction materials such as Cu2O.

  • 50. Rengaraj, Selvaraj
    et al.
    Venkataraj, Selvaraj
    Jee, Sun Hee
    Kim, Younghun
    Tai, Cheuk-wai
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK), Avdelningen för oorganisk kemi och strukturkemi.
    Repo, Eveliina
    Koistinen, Arto
    Ferancova, Adriana
    Sillanpaa, Mika
    Cauliflower-like CdS Microspheres Composed of Nanocrystals and Their Physicochemical Properties2011Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 27, nr 1, s. 352-358Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cauliflower-like cadmium sulfide (CdS) microspheres composed of nanocrystals have been successfully synthesized by a hydrothermal method using poly(ethylene glycol) (PEG) as the template coordination agent and characterized by a variety of methods. Our experiments confirmed that the size of the CdS microspheres could be easily modified by controlling the chain length of PEG. Powder X-ray diffraction and Raman spectroscopy measurements revealed the cubic structure of the CdS microspheres; morphological studies performed by HR-SEM and HR-TEM methods showed the cauliflower-like structure of the synthesized CdS microspheres. Each microsphere was identified to be created by the self-assembly of CdS nanocrystals and is attributed to the oriented aggregation of the CdS nanocrystals around a polymer-Cd(2+) complex spherical framework structure. X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray (EDX) analysis confirmed the stoichiometries of the CdS microspheres. Diffuse reflectance spectrum (DRS) measurements showed that increasing the PEG chain length increased the band gap value of the CdS microspheres slightly, from 1.99 to 2.06 eV. The cauliflower-like CdS microspheres could be applied to photocatalytic degradation studies.

12 1 - 50 of 93
RefereraExporteraLink til resultatlisten
Permanent link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf