材料科学
电解
同步加速器
图层(电子)
形态学(生物学)
催化作用
电解水
化学工程
复合材料
光学
化学
电极
地质学
物理
工程类
生物化学
电解质
物理化学
古生物学
作者
Jason Keonhag Lee,Pascal J. Kim,Kevin M. Krause,Pranay Shrestha,Manojkumar Balakrishnan,Kieran F. Fahy,Khalid Fatih,Nima Shaigan,Mingyuan Ge,Wah-Keat Lee,Aimy Bazylak
标识
DOI:10.1016/j.xcrp.2022.101232
摘要
The limited availability of iridium in the Earth’s crust poses severe challenges to establishing gigawatt-scale electrolyzers that are needed for energy storage; this problem urgently calls for reduced iridium loadings. Reducing iridium loadings requires catalyst structure optimization, but to date, little attention has been paid to the characterization of electron, proton, and mass transport in the catalyst layer, particularly at the nanoscale. We present the 3D nanoscale pore structure of iridium-based catalyst layers via synchrotron full-field transmission X-ray microscopy (TXM) and perform pore network modeling to determine effective transport properties in water electrolyzers. We observe a wide range of pore sizes in the catalyst layer, constituting pathways that facilitate mass transport. Increasing the thickness of the ionomer layer that covers the catalyst particles significantly increases protonic conductivity at the cost of reducing the open pore space and electrical conductivity, both of which are detrimental to electrolyzer performance.
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