Yu Weilai, Young James L, Deutsch Todd G, Lewis Nathan S
Division of Chemistry and Chemical Engineering and Beckman Institute, California Institute of Technology, Pasadena, California 91125, United States.
Chemistry and Nanoscience Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
ACS Appl Mater Interfaces. 2021 Dec 8;13(48):57350-57361. doi: 10.1021/acsami.1c18243. Epub 2021 Nov 25.
The long-term stability in acidic or alkaline aqueous electrolytes of p-GaInP photocathodes, with a band gap of ∼1.8 eV, for the solar-driven hydrogen-evolution reaction (HER) has been evaluated from a thermodynamic, kinetic, and mechanistic perspective. At either pH 0 or pH 14, etched p-GaInP electrodes corroded cathodically under illumination and formed metallic In on the photoelectrode surface. In contrast, under the same conditions, electrodeposition of Pt facilitated the HER kinetics and stabilized p-GaInP/Pt photoelectrodes against such cathodic decomposition. When held at 0 V versus the reversible hydrogen electrode, p-GaInP/Pt electrodes in either pH = 0 or pH = 14 exhibited stable current densities () of ∼-9 mA cm for hundreds of hours under simulated 1 sun illumination. During the stability tests, the current density-potential (-) characteristics of the p-GaInP/Pt photoelectrodes degraded due to pH-dependent changes in the surface chemistry of the photocathode. This work provides a fundamental understanding of the stability and corrosion mechanisms of p-GaInP photocathodes that constitute a promising top light absorber for tandem solar-fuel generators.
对于带隙约为1.8 eV的p-GaInP光阴极在酸性或碱性水性电解质中用于太阳能驱动析氢反应(HER)的长期稳定性,已从热力学、动力学和机理角度进行了评估。在pH 0或pH 14时,经蚀刻的p-GaInP电极在光照下发生阴极腐蚀,并在光电极表面形成金属铟。相比之下,在相同条件下,铂的电沉积促进了HER动力学,并使p-GaInP/Pt光电极免受这种阴极分解的影响。当相对于可逆氢电极保持在0 V时,pH = 0或pH = 14的p-GaInP/Pt电极在模拟1个太阳光照下数百小时内表现出约-9 mA cm²的稳定电流密度()。在稳定性测试期间,由于光阴极表面化学性质随pH值的变化,p-GaInP/Pt光电极的电流密度-电势(-)特性发生了退化。这项工作为p-GaInP光阴极的稳定性和腐蚀机理提供了基本认识,p-GaInP光阴极是串联太阳能燃料发生器中一种很有前景的顶部光吸收体。