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Metal dichalcogenides are promising electrocatalysts for hydrogen evolution, but more active and stable materials are desired. Here the authors demonstrate that H-TaS2 and H-NbS2 possess high basal-plane activity that increases with cycling through changes in the morphology of the catalysts.
Regulating guest access and release in porous materials remains an important goal. Here, May and colleagues elucidate the mechanism by which guest admission can be temperature-regulated in typical microporous materials, and experimentally exploit this process to achieve appreciable and reversible hydrogen storage.
Transition-metal dichalcogenides are appealing catalysts for H2 generation from water. They tend to rely on scarce edge sites, rather than the more abundant basal-plane sites, to drive catalysis. Now, guided by computation, H-TaS2 and H-NbS2 are proposed as highly basal-plane-active catalysts that improve with electrochemical cycling.
Multiple exciton generation, in which two electron–hole pairs are generated from the absorption of one high-energy photon, has been demonstrated to improve efficiency in quantum-dot-based solar cells. Now, a photoelectrochemical system using PbS quantum dots is shown to drive hydrogen evolution with external quantum efficiency over 100%.
Organolead halide perovskite solar absorbers demonstrate high photovoltaic efficiencies but they are notorious for their intolerance to water. Now, methylammonium lead iodide perovskites are used to harvest solar energy — in water — via photocatalytic generation of hydrogen from solutions of hydriodic acid.