Perovskite Catalysts for Pure-Water-Fed Anion-Exchange-Membrane Electrolyzer Anodes: Co-Design of Electrically Conductive Nanoparticle Cores and Active Surfaces

10 February 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Anion-exchange-membrane water electrolyzers (AEMWEs) are a possible low-capital expense, efficient, and scalable hydrogen-production technology with inexpensive hardware, earth-abundant catalysts, and pure-water. However, pure-water-fed AEMWEs are still at an early stage of development and suffer from inferior performance compared to proton-exchange-membrane water electrolyzers (PEMWEs). One key challenge is to develop effective non-platinum group metal (non-PGM) anode catalysts and electrodes in pure-water-fed AEMWEs. We show how LaNiO3-based perovskite oxides can be tuned by co-substitution on both A- and B-sites to simultaneously maintain high metallic electrical conductivity along with controlled surface reconstruction to expose stable Co-based active catalyst. The optimized perovskite, Sr0.1La0.9Co0.5Ni0.5O3, yielded pure-water AEMWEs operating at 1.97 V at 2 A cm–2 at 70 oC with pure-water feed, thus illustrating the utility of the catalyst design principles.

Supplementary materials

Title
Description
Actions
Title
Supplementary Information
Description
Methods for preparation and characterization of perovskite catalysts; methods for electrode and MEA assembly preparation; electrochemical measurement methods for AEMWE operation and three-electrode cell tests; powder XRD patterns; SEM images along with corresponding particle size distribution analysis; polarization curves in AEMWE single-cell configuration; double-layer capacitance (Cdl) measurements; durability tests; and characterization data from ICP-MS, BET, and XPS measurements.
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.