析氧
电催化剂
电解
阳极
化学工程
电解水
分解水
催化作用
材料科学
阴极
制氢
多孔性
离子交换
膜
无机化学
化学
电极
离子
电化学
复合材料
有机化学
物理化学
工程类
电解质
光催化
生物化学
作者
Binyu Chen,Ana Laura G. Biancolli,Chase L. Radford,Steven Holdcroft
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-05-22
卷期号:8 (6): 2661-2667
被引量:24
标识
DOI:10.1021/acsenergylett.3c00878
摘要
Anion-exchange membrane water electrolysis (AEMWE) is a promising technology for low-cost, high-efficiency, green hydrogen production. The stability of the AEM is a critical issue but difficult to delineate in situ from degradation of the catalyst layer (CL). Moreover, the porous transport layer (PTL) can contribute electrocatalytically. Herein, we demonstrate that stainless steel (SS) felt, in the absence of an anode CL, is highly active toward the oxygen evolution reaction (OER) (1 A cm–2 at 1.74 Vcell) and serves as a combined OER electrocatalyst and PTL, thus simplifying the study of AEMs in water electrolyzers. We further show that Ni felt exhibits much lower OER activity than SS felt, which suggests that in situ studies of OER electrocatalysts and CL compositions should be performed with Ni felt, not SS felt, to reduce OER contributions from the PTL. Lastly, we found that the substrate for depositing the cathode CL, AEM, or PTL strongly influences the rate of H2 crossover.
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