催化作用
阳极
电解
电导率
化学工程
材料科学
催化剂载体
无机化学
膜电极组件
化学
电极
有机化学
电解质
工程类
物理化学
作者
Melissa E. Kreider,Haoran Yu,Luigi Osmieri,Makenzie Parimuha,Kimberly S. Reeves,Daniela H. Marin,Ryan T. Hannagan,Emily K. Volk,Thomas F. Jaramillo,James L. Young,Piotr Zelenay,Shaun M Alia
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-07-03
卷期号:14 (14): 10806-10819
被引量:33
标识
DOI:10.1021/acscatal.4c02932
摘要
Anion exchange membrane water electrolysis (AEMWE) is a promising technology to produce hydrogen from low-cost, renewable power sources. Recently, the efficiency and durability of AEMWE have improved significantly due to advances in the anion exchange polymers and catalysts. To achieve performances and lifetimes competitive with proton exchange membrane or liquid alkaline electrolyzers, however, improvements in the integration of materials into the membrane electrode assembly (MEA) are needed. In particular, the integration of the oxygen evolution reaction (OER) catalyst, ionomer, and transport layer in the anode catalyst layer has significant impacts on catalyst utilization and voltage losses due to the transport of gases, hydroxide ions, and electrons within the anode. This study investigates the effects of the properties of the OER catalyst and the catalyst layer morphology on performance. Using cross-sectional electron microscopy and in-plane conductivity measurements for four PGM-free catalysts, we determine the catalyst layer thickness, uniformity, and electronic conductivity and further use a transmission line model to relate these properties to the catalyst layer resistance and utilization. We find that increased loading is beneficial for catalysts with high electronic conductivity and uniform catalyst layers, resulting in up to 55% increase in current density at 2 V due to decreased kinetic and catalyst layer resistance losses, while for catalysts with lower conductivity and/or less uniform catalyst layers, there is minimal impact. This work provides important insights into the role of catalyst layer properties beyond intrinsic catalyst activity in AEMWE performance.
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