Challenges and strategies for probing the composite interface of PEM electrolyzers and fuel cells using operando AP-XPS

Journal Article · Tue Dec 31 19:00:00 EST 2024 · Journal of Materials Chemistry A

DOI:https://doi.org/10.1039/d4ta07085b· OSTI ID:2584097

Hamlyn, Rebecca; Mahl, Johannes; Zhang, Xueqiang; English, Damon; McAfee, Terry; Crumlin, Ethan J

Left: cross-section schematic of a membrane electrode assembly, the working electrode changing state with applied potential. Center: the operando cell design that enables snapshot data acquisition during trajectory movement. Right: resulting spectra. Understanding the surface chemistry of electrocatalyst systems under operando conditions is central to revealing the electrocatalytic cell's working mechanisms. Determination of these catalytic processes on a molecular scale and the involved components is fundamental to streamlining material design for energy conversion and storage applications. X-ray photoelectron spectroscopy (XPS) is an established technique used to study the chemical and electronic states of materials. While the surface sensitivity of XPS is typically high, use of tender X-ray energies and technical advancements have allowed for the direct probing of solid–vapor and solid–liquid interfaces. However, protocols and documentation of experimental considerations for operando XPS probing of working electrolyzers and fuel cells remain scarce. Herein, we report an approach for the study of working polymer electrolyte membrane (PEM) electrolysis cells using ambient pressure X-ray photoelectron spectroscopy (AP-XPS). This approach directly probes the composite electrode surface on the membrane electrode assembly (MEA) in 100% relative humidity to establish a meaningful liquid layer for electrocatalysis. We carry out a systematic investigation from the cell constituent components to a fully assembled working operando electrolytic system and establish a method for AP-XPS study of the complex composite MEA, providing recommendations for data acquisition and component analysis.

• Research Organization: Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
• Sponsoring Organization: US Department of Energy; USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22), Chemical Sciences, Geosciences & Biosciences Division (SC-22.1)
• Grant/Contract Number: AC02-05CH11231
• OSTI ID: 2584097
• Journal Information: Journal of Materials Chemistry A, Journal Name: Journal of Materials Chemistry A Journal Issue: 27 Vol. 13
• Country of Publication: United States
• Language: English