Modular Solar-to-Fuel Electrolysis at Low Cell Potentials Enabled by Glycerol Electrooxidation and a Bipolar Membrane Separator.

Solar fuel generation through water electrolysis or electrochemical CO reduction is thermodynamically limited when it is paired with oxygen evolution reaction (OER). Glycerol electrooxidation reaction (GEOR) is an alternative anodic reaction with lower anodic electrochemical potential that utilizes a renewable coproduct produced during biodiesel synthesis. We show that GEOR on an Au-Pt-Bi ternary metal electrocatalyst in a model alkaline crude glycerol solution can provide significant cell potential reductions even when paired to reduction reactions in seawater and acidic catholytes via a bipolar membrane (BPM).

Quaternary Core-Shell Oxynitride Nanowire Photoanode Containing a Hole-Extraction Gradient for Photoelectrochemical Water Oxidation.

A nanowire photoanode SrTaON, a semiconductor suitable for overall water-splitting with a band gap of 2.3 eV, was coated with functional overlayers to yield a core-shell structure while maintaining its one-dimensional morphology. The nanowires were grown hydrothermally on tantalum, and the perovskite-related oxynitride structure was obtained by nitridation.

Enhanced Electrochemical Stability of TiO-Protected, Al-doped ZnO Transparent Conducting Oxide Synthesized by Atomic Layer Deposition.

Transparent, conductive coatings on porous, three-dimensional materials are often used as the current collector for photoelectrode designs in photoelectrochemical applications. These structures allow for improved light trapping and absorption in chemically synthesized, photoactive overlayers while minimizing parasitic absorption in the current collecting layer. Atomic layer deposition (ALD) is particularly useful for fabricating transparent conducting oxides (TCOs) like Sn-doped InO (ITO) and Al-doped ZnO (AZO) for structured materials because the deposition is specific to exposed surfaces.

Inhibition of Tafel Kinetics for Electrolytic Hydrogen Evolution on Isolated Micron Scale Electrocatalysts on Semiconductor Interfaces.

Semiconductor-liquid junctions are ubiquitous in photoelectrochemical approaches to artificial photosynthesis. By analogy with the antennae and reaction centers in natural photosynthetic complexes, separating the light-absorbing semiconductor and electrocatalysts can improve catalytic efficiency. A catalytic layer can also impair the photovoltage-generating energetics of the electrode without appropriate microscopic organization of catalytically active area on the surface.