Abstract
The long-term stability for the hydrogen-evolution reaction (HER) of homojunction pn+-Ga0.52In0.48P photocathodes (band gap = 1.8 eV) with an electrodeposited Pt catalyst (pn+-GaInP/Pt) has been systematically evaluated in both acidic and alkaline electrolytes. Electrode dissolution during chronoamperometry was correlated with changes over time in the current density-potential (J-E) behavior to reveal the underlying failure mechanism. Pristine pn+-GaInP/Pt photocathodes yielded an open-circuit photopotential (Eoc) as positive as >1.0 V vs the potential of the reversible hydrogen electrode (RHE) and a light-limited current density (Jph) of >12 mA cm-2(1-sun illumination). However, Eocand Jphgradually degraded at either pH 0 or pH 14. The performance degradation was attributed to three different failure modes: (1) gradual thinning of the n+-emitter layer due to GaInP dissolution in acid; (2) active corrosion of the underlying GaAs substrate at positive potentials causing delamination of the upper GaInP epilayers; and (3) direct GaAs/electrolyte contact compromising the operational stability of the device. This work reveals the importance of both substrate stability and structural integrity of integrated photoelectrodes toward stable solar fuel generation.
Original language | American English |
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Pages (from-to) | 26622-26630 |
Number of pages | 9 |
Journal | ACS Applied Materials and Interfaces |
Volume | 14 |
Issue number | 23 |
DOIs | |
State | Published - 15 Jun 2022 |
Bibliographical note
Publisher Copyright:© 2022 American Chemical Society. All rights reserved.
NREL Publication Number
- NREL/JA-5900-83272
Keywords
- failure mode
- III-V semiconductor
- photoelectrochemistry
- solar fuels
- water splitting