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Title: Investigations of the stability of GaAs for photoelectrochemical H2 evolution in acidic or alkaline aqueous electrolytes

Abstract

The long-term stability of p-GaAs photocathodes has been investigated for the hydrogen-evolution reaction (HER) in contact with either 1.0 M H2SO4(aq) or 1.0 M KOH(aq). Stability for the HER was evaluated using p-GaAs electrodes that were either etched or coated with active HER catalysts (Pt and CoP). Changes in surface characteristics of GaAs after exposure to electrochemical conditions were monitored by X-ray photoelectron spectroscopy (XPS), and electrode dissolution processes were evaluated by inductively coupled plasma mass spectrometry (ICP-MS). Consistent with thermodynamic predictions, after operation of the HER at pH 0 or pH 14, illuminated etched p-GaAs electrodes exhibited minimal dissolution while preserving a nearly stoichiometric surface. Electrodeposition or sputtering of Pt on the p-GaAs surface promoted the formation of excess As0via an interfacial reaction during the HER. The resulting non-stoichiometric As0-rich surface of p-GaAs/Pt electrodes caused a loss in photoactivity as well as substantial cathodic dark current. In contrast, p-GaAs electrodes coated with thin-film CoP catalysts did not display an increase in surficial As0 after operation of the HER in acidic electrolytes. Minimization of deleterious interfacial reactions is thus critical to obtain extended stability in conjunction with high performance from p-GaAs photocathodes.

Authors:
ORCiD logo [1]; ORCiD logo [1];  [1]; ORCiD logo [2]; ORCiD logo [2]
  1. California Institute of Technology (CalTech), Pasadena, CA (United States)
  2. California Institute of Technology (CalTech), Pasadena, CA (United States). Beckman Institute
Publication Date:
Research Org.:
California Institute of Technology (CalTech), Pasadena, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
OSTI Identifier:
1978835
Alternate Identifier(s):
OSTI ID: 1823680
Grant/Contract Number:  
SC0004993; SC0022087
Resource Type:
Accepted Manuscript
Journal Name:
Journal of Materials Chemistry. A
Additional Journal Information:
Journal Volume: 9; Journal Issue: 40; Journal ID: ISSN 2050-7488
Publisher:
Royal Society of Chemistry
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 36 MATERIALS SCIENCE; 32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION

Citation Formats

Yu, Weilai, Richter, Matthias H., Simonoff, Ethan, Brunschwig, Bruce S., and Lewis, Nathan S. Investigations of the stability of GaAs for photoelectrochemical H2 evolution in acidic or alkaline aqueous electrolytes. United States: N. p., 2021. Web. doi:10.1039/d1ta04145b.
Yu, Weilai, Richter, Matthias H., Simonoff, Ethan, Brunschwig, Bruce S., & Lewis, Nathan S. Investigations of the stability of GaAs for photoelectrochemical H2 evolution in acidic or alkaline aqueous electrolytes. United States. https://doi.org/10.1039/d1ta04145b
Yu, Weilai, Richter, Matthias H., Simonoff, Ethan, Brunschwig, Bruce S., and Lewis, Nathan S. Wed . "Investigations of the stability of GaAs for photoelectrochemical H2 evolution in acidic or alkaline aqueous electrolytes". United States. https://doi.org/10.1039/d1ta04145b. https://www.osti.gov/servlets/purl/1978835.
@article{osti_1978835,
title = {Investigations of the stability of GaAs for photoelectrochemical H2 evolution in acidic or alkaline aqueous electrolytes},
author = {Yu, Weilai and Richter, Matthias H. and Simonoff, Ethan and Brunschwig, Bruce S. and Lewis, Nathan S.},
abstractNote = {The long-term stability of p-GaAs photocathodes has been investigated for the hydrogen-evolution reaction (HER) in contact with either 1.0 M H2SO4(aq) or 1.0 M KOH(aq). Stability for the HER was evaluated using p-GaAs electrodes that were either etched or coated with active HER catalysts (Pt and CoP). Changes in surface characteristics of GaAs after exposure to electrochemical conditions were monitored by X-ray photoelectron spectroscopy (XPS), and electrode dissolution processes were evaluated by inductively coupled plasma mass spectrometry (ICP-MS). Consistent with thermodynamic predictions, after operation of the HER at pH 0 or pH 14, illuminated etched p-GaAs electrodes exhibited minimal dissolution while preserving a nearly stoichiometric surface. Electrodeposition or sputtering of Pt on the p-GaAs surface promoted the formation of excess As0via an interfacial reaction during the HER. The resulting non-stoichiometric As0-rich surface of p-GaAs/Pt electrodes caused a loss in photoactivity as well as substantial cathodic dark current. In contrast, p-GaAs electrodes coated with thin-film CoP catalysts did not display an increase in surficial As0 after operation of the HER in acidic electrolytes. Minimization of deleterious interfacial reactions is thus critical to obtain extended stability in conjunction with high performance from p-GaAs photocathodes.},
doi = {10.1039/d1ta04145b},
journal = {Journal of Materials Chemistry. A},
number = 40,
volume = 9,
place = {United States},
year = {Wed Sep 22 00:00:00 EDT 2021},
month = {Wed Sep 22 00:00:00 EDT 2021}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record

Figures / Tables:

Figure 1 Figure 1: Corrosion rates of p-GaAs at the open-circuit potential (Eoc) in the dark. Comparison of (a,d) the measured Eoc values versus time in the dark, and the corrosion thickness of GaAs based on the concentrations of (b,e) Ga ions and (c,f) As ions in (a-c) 1.0 M H2SO4(aq) andmore » (d-f) 1.0 M KOH(aq).« less

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