材料科学
化学工程
阳极
纳米孔
电解质
氧化物
电化学
聚合物电解质膜电解
膜
可逆氢电极
电解水
电导率
纳米技术
无机化学
电解
工作电极
电极
冶金
有机化学
催化作用
物理化学
生物化学
工程类
化学
作者
Swarnendu Chatterjee,Xiong Peng,Saad Intikhab,Guosong Zeng,Nancy N. Kariuki,Deborah J. Myers,Nemanja Danilovic,Joshua Snyder
标识
DOI:10.1002/aenm.202101438
摘要
Abstract The growth of the hydrogen economy is predicated on advancements in electrochemical energy technologies, with water electrolysis as a key component to the technological portfolio. Much of the focus on anode catalyst development for polymer electrolyte membrane water electrolyzers (PEMWE) is centered on activity as controlled by compositional and morphological impacts on reactant/intermediate/product adsorption. However, the effectiveness of this strategy is found to be limited upon integration of these materials into PEMWE membrane electrode assemblies (MEA). Regardless of catalyst activity, the combination of electrode inhomogeneity, ionomer integration, and high density of oxide–oxide interfaces yields significant performance losses associated with poor catalytic electrode conductivity. Here many of these limitations are addressed through the development of a unique catalyst morphology composed of nanoporous Ir nanosheets (npIr x ‐NS) that exhibit high catalytic activity for the anodic oxygen evolution reaction and superior electrode electronic conductivity in comparison to a commercial IrO 2 nanoparticle catalyst. The utility of the npIr x ‐NS is demonstrated through incorporation into PEMWE MEAs where their performance exceeds that of commercial catalyst coated membranes at loadings as low as 0.06 mg Ir cm −2 while exhibiting a negligible loss in performance following 50 000 accelerated stress test cycles.
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