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| 3. |
- Valdes, A., et al.
(författare)
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Solar hydrogen production with semiconductor metal oxides: new directions in experiment and theory
- 2012
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Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9084 .- 1463-9076. ; 14:1, s. 49-70
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Forskningsöversikt (refereegranskat)abstract
- An overview of a collaborative experimental and theoretical effort toward efficient hydrogen production via photoelectrochemical splitting of water into di-hydrogen and di-oxygen is presented here. We present state-of-the-art experimental studies using hematite and TiO(2) functionalized with gold nanoparticles as photoanode materials, and theoretical studies on electro and photo-catalysis of water on a range of metal oxide semiconductor materials, including recently developed implementation of self-interaction corrected energy functionals.
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| 4. |
- Zhu, Jiefang, 1973, et al.
(författare)
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Nanostructured materials for photocatalytic hydrogen production
- 2009
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Ingår i: Current Opinion in Colloid and Interface Science. - : Elsevier BV. - 1359-0294 .- 1879-0399. ; 14:4, s. 260-269
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Tidskriftsartikel (refereegranskat)abstract
- Photocatalytic hydrogen (H-2) production represents a very promising but challenging contribution to a clean, sustainable and renewable energy system. The photocatalyst material plays a key role in photocatalytic H-2 production, and it has proven difficult to obtain corrosion resistant, chemically stable, visible light harvesting and highly efficient photocatalysts, which have their band edges matching the O-2 and H-2 production levels. Nanoscience and nanotechnology are opening a new vista in the development of highly active, nanostructured photocatalysts with large surface areas for optimized light absorption, minimized distances (or times) for charge-carrier transport, and further favorable properties. Our focus here is on recently developed nanostructured photocatalysts. In particular. the particle size, chemical composition (including dopants), microstructure, crystal phase. morphology, surface modification, bandgap and flat-band potential of the nanophotocatalysts have shown a visible effect on photocatalytic H-2 production rates, which may be further increased by adding sensitizers, cocatalysts or scavengers. Finally, potential directions required to push this research field a step further are highlighted. (
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| 6. |
- Antosiewicz, Tomasz, 1981, et al.
(författare)
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Oscillatory Optical Response of an Amorphous Two-Dimensional Array of Gold Nanoparticles
- 2012
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Ingår i: Physical Review Letters. - 1079-7114 .- 0031-9007. ; 109:24
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Tidskriftsartikel (refereegranskat)abstract
- The optical response of metallic nanoparticle arrays is dominated by localized surface plasmon excitations and is the sum of individual particle contributions modified by interparticle coupling that depends on specific array geometry. We demonstrate a so far unexplored distinct oscillatory behavior of the plasmon peak position, full width at half maximum, and extinction efficiency in large area amorphous arrays of Au nanodisks, which depend on the minimum particle center-to-center distance in the array. Amorphous arrays exhibit short-range order and are completely random at long distances. In our theoretical analysis we introduce a film of dipoles approach, within the framework of the coupled dipole approximation, which describes the array as an average particle surrounded by a continuum of dipoles with surface densities determined by the pair correlation function of the array.
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| 7. |
- Briand, Elisabeth, 1979, et al.
(författare)
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Combined QCM-D and EIS study of supported lipid bilayer formation and interaction with pore-forming peptides
- 2010
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Ingår i: The Analyst. - : Royal Society of Chemistry (RSC). - 0003-2654 .- 1364-5528. ; 135:2, s. 343-350
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Tidskriftsartikel (refereegranskat)abstract
- A novel set-up combining the quartz crystal microbalance with dissipation monitoring technique (QCM-D) and electrochemical impedance spectroscopy (EIS) under flow conditions was successfully used to follow supported lipid bilayer (SLB) formation on SiO(2). This study demonstrates the simultaneous detection, in real time, of both the electrical and the structural properties of the SLB. The combination of the two techniques provided novel insights regarding the mechanism of SLB formation: we found indications for an annealing process of the lipid alkyl chains after the mass corresponding to complete bilayer coverage had been deposited. Moreover, the interaction of the SLB with the pore-forming toxin, gramicidin D (grD) was studied for grD concentrations ranging from 0.05 to 40 mg L(-1). Membrane properties were altered depending on the toxin concentration. For low grD concentrations, the electrical properties of the SLB changed upon insertion of active ion channels. For higher concentrations, the QCM-D data showed dramatic changes in the viscoelastic properties of the membrane while the EIS spectra did not change. AFM confirmed significant structural changes of the membrane at higher grD concentrations. Thus, the application of combined QCM-D and EIS detection provides complementary information about the system under study. This information will be particularly important for the continued detailed investigation of interactions at model membrane surfaces
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| 8. |
- Chakraborty, S., et al.
(författare)
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Mechanistic Insight into the Structure and Dynamics of Entangled and Hydrated lambda-Phage DNA
- 2012
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Ingår i: Journal of Physical Chemistry A. - : American Chemical Society (ACS). - 1089-5639 .- 1520-5215. ; 116:17, s. 4274-4284
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Tidskriftsartikel (refereegranskat)abstract
- Intrinsic dynamics of DNA plays a crucial role in DNA protein interactions and has been emphasized as a possible key component for in vivo chromatin organization. We have prepared an entangled DNA microtube above the overlap concentration by exploiting the complementary cohesive ends of lambda-phage DNA, which is confirmed by atomic force microscopy and agarose gel electrophoresis. Photon correlation spectroscopy further confirmed that the entangled solutions are found to exhibit the classical hydrodynamics of a single chain segment on length scales smaller than the hydrodynamic length scale of single lambda-phage DNA molecule. We also observed that in 41.6% (gm water/gm DNA) hydrated state, lambda-phage DNA exhibits a dynamic transition temperature (T-dt) at 187 K and a crossover temperature (T-c) at 246 K. Computational insight reveals that the observed structure and dynamics of entangled lambda-phage DNA are distinctively different from the behavior of the corresponding unentangled DNA with open cohesive ends, which is reminiscent with our experimental observation.
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| 9. |
- Churchard, A. J., et al.
(författare)
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A multifaceted approach to hydrogen storage
- 2011
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Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9084 .- 1463-9076. ; 13:38, s. 16955-16972
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Tidskriftsartikel (refereegranskat)abstract
- The widespread adoption of hydrogen as an energy carrier could bring significant benefits, but only if a number of currently intractable problems can be overcome. Not the least of these is the problem of storage, particularly when aimed at use onboard light-vehicles. The aim of this overview is to look in depth at a number of areas linked by the recently concluded HYDROGEN research network, representing an intentionally multi-faceted selection with the goal of advancing the field on a number of fronts simultaneously. For the general reader we provide a concise outline of the main approaches to storing hydrogen before moving on to detailed reviews of recent research in the solid chemical storage of hydrogen, and so provide an entry point for the interested reader on these diverse topics. The subjects covered include: the mechanisms of Ti catalysis in alanates; the kinetics of the borohydrides and the resulting limitations; novel transition metal catalysts for use with complex hydrides; less common borohydrides; protic-hydridic stores; metal ammines and novel approaches to nano-confined metal hydrides.
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| 10. |
- Dahlin, Andreas, 1980, et al.
(författare)
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Localized surface plasmon sensing of lipid-membrane-mediated biorecognition events
- 2005
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 127:14, s. 5043-5048
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Tidskriftsartikel (refereegranskat)abstract
- Supported phospholipid bilayers (SPBs) have emerged as important model systems for studies of the natural cell membrane and its components, which are essential for the integrity and function of cells in all living organisms, and also constitute common targets for therapeutic drugs and in disease diagnosis. However, the preferential occurrence of spontaneous SPB formation on silicon-based substrates, but not on bare noble-metal surfaces, has so far excluded the use of the localized surface plasmon resonance (LSPR) sensing principle for studies of lipid-membrane-mediated biorecognition reactions. This is because the LSPR phenomenon is associated with, and strongly confined to, the interfacial region of nanometric noble-metal particles. This problem has been overcome in this study by a self-assembly process utilizing localized rupture of phospholipid vesicles on silicon dioxide in the bottom of nanometric holes in a thin gold film. The hole-induced localization of the LSPR field to the voids of the holes is demonstrated to provide an extension of the LSPR sensing concept to studies of reactions confined exclusively to SPB-patches supported on SiO2. In particular, we emphasize the possibility of performing label-free studies of lipid-membrane-mediated reaction kinetics, including the compatibility of the assay with array-based reading (similar to 7 x 7 mu m(2)) and detection of signals originating from bound protein in the zeptomole regime.
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