journal article·2021-12-08Open access

Understanding the Stability of Etched or Platinized p-GaInP Photocathodes for Solar-Driven H2 Evolution

Weilai Yu, James L. Young, Todd G. Deutsch, Nathan S. Lewis

ACS Applied Materials & Interfaces· Volume 13· Issue 48

Abstract

The long-term stability in acidic or alkaline aqueous electrolytes of p-Ga0.52In0.48P 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 In0 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 (J) of ∼−9 mA cm–2 for hundreds of hours under simulated 1 sun illumination. During the stability tests, the current density–potential (J–E) 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.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Chalcogenide Semiconductor Thin Films · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

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

Funding

U.S. Department of Energy

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