Ligand-Tuned AgBiS Planar Heterojunctions Enable Efficient Ultrathin Solar Cells.

AgBiS quantum dots (ABS QDs) have emerged as highly promising candidates for photovoltaic applications due to their strong sunlight absorption, nontoxicity, and elemental availability. Nevertheless, the efficiencies of ABS solar cells currently fall far short of their thermodynamic limits due in large part to sluggish charge transport characteristics in nanocrystal-derived films. In this study, we overcome this limitation by tuning the surfaces of ABS semiconductor QDs via a solvent-induced ligand exchange (SILE) strategy and provide key insights into the role of surface composition on both - and -type charge transfer doping, as well as long-range charge transport.

Electrochemical versus Photoelectrochemical Water Oxidation Kinetics on Bismuth Vanadate (Photo)anodes.

This study reports a comparison of the kinetics of electrochemical (EC) versus photoelectrochemical (PEC) water oxidation on bismuth vanadate (BiVO) photoanodes. Plots of current density versus surface hole density, determined from operando optical absorption analyses under EC and PEC conditions, are found to be indistinguishable. We thus conclude that EC water oxidation is driven by the Zener effect tunneling electrons from the valence to conduction band under strong bias, with the kinetics of both EC and PEC water oxidation being determined by the density of accumulated surface valence band holes.

Tuning Carbon Dioxide Reduction Reaction Selectivity of Bi Single-Atom Electrocatalysts with Controlled Coordination Environments.

Control over product selectivity of the electrocatalytic CO reduction reaction (CORR) is a crucial challenge for the sustainable production of carbon-based chemical feedstocks. In this regard, single-atom catalysts (SACs) are promising materials due to their tunable coordination environments, which could enable tailored catalytic activities and selectivities, as well as new insights into structure-activity relationships. However, direct evidence for selectivity control via systematic tuning of the SAC coordination environment is scarce.

Mesoporous WO/TiO spheres with tailored surface properties for concurrent solar photocatalysis and membrane filtration.

The strategical integration of membrane water filtration with semiconductor photocatalysis presents a frontier in deep purification with a self-cleaning capability. However, the membrane fouling caused by the cake layer of the reclaimed TiO nanoparticles is a key obstacle. Herein, mesoporous WO/TiO spheres (∼450 nm in diameter) consisting of numerous self-assembled WO-decoated anatase TiO nanocrystallites are successfully prepared via a facile wet-chemistry route.