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 |
|---|---|
| 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.
NLR Publication Number
- NREL/JA-5900-83272
Keywords
- failure mode
- III-V semiconductor
- photoelectrochemistry
- solar fuels
- water splitting