析氧
电解
电解水
材料科学
分解水
制氢
化学工程
聚合物电解质膜电解
催化作用
过渡金属
碱性水电解
氢
降级(电信)
无机化学
高压电解
瓶颈
金属
电极
氧气
电解质
电流(流体)
阳极
杂质
电解法
克拉克电极
化学
大规模运输
冶金
水处理
锅炉给水
作者
Max Pupucevski,Judith Lattimer,Emily Tong,Anna Wolock,Angeles Dios,Steve McCatty
出处
期刊:Meeting abstracts
日期:2025-11-24
卷期号:MA2025-02 (39): 1888-1888
标识
DOI:10.1149/ma2025-02391888mtgabs
摘要
Achieving cost-effective and durable water electrolysis using widely available, minimally purified water is a central challenge for large-scale hydrogen production. A major bottleneck lies in developing robust oxygen evolution reaction (OER) catalysts that can maintain high activity and stability while operating in water containing dissolved salts and other contaminants. To address this, we have designed and synthesized non-platinum group metal (PGM) OER electrodes—including novel monolithic metal oxides deposited on stainless-steel or Hastelloy substrates—tailored to withstand harsh electrolyzer conditions without significant performance loss. By optimizing catalyst composition, ionomer content, and mass transport within the electrode, we aim to achieve current densities exceeding 2 A cm⁻² at 1.8 V or less while ensuring minimal degradation rates in alkaline environments with salt concentrations of at least 1000 ppm. Full-cell tests conducted in 5 cm² anion-exchange membrane electrolyzers demonstrate that these advanced OER catalysts, when paired with PGM-free cathodes, deliver stable performance across multiple impurity levels (e.g., up to 1000 ppm NaCl) in 0.1 M KOH at 80 °C. Notably, current densities exceeding 1.5 A cm⁻² at 2 V have been achieved under both tap-water and brinier feeds, validating the feasibility of durable, high-performance operation on low-grade water. Ongoing work focuses on optimizing catalyst-layer morphology, catalyst-ionomer interactions, and active-area scale-up to improve electrolyzer resiliency and cost-effectiveness, paving the way for commercially viable hydrogen production from impure water streams.
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