催化作用
析氧
碳纤维
扩散
锡
化学工程
色散(光学)
气体扩散电极
化学
电极
氧化物
氧气
氧化锡
材料科学
纳米技术
电化学
物理化学
有机化学
热力学
复合材料
光学
物理
工程类
复合数
作者
Aline Bornet,Rebecca K. Pittkowski,Tobias Mølgaard Nielsen,Etienne Berner,Annabelle Maletzko,Johanna Schröder,Jonathan Quinson,Julia Melke,Kirsten M. Ø. Jensen,Matthias Arenz
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2023-05-22
卷期号:13 (11): 7568-7577
被引量:29
标识
DOI:10.1021/acscatal.3c01193
摘要
High Resolution Image Download MS PowerPoint Slide State-of-the-art industrial electrocatalysts for the oxygen evolution reaction (OER) under acidic conditions are Ir-based. Considering the scarce supply of Ir, it is imperative to use the precious metal as efficiently as possible. In this work, we immobilized ultrasmall Ir and Ir 0.4 Ru 0.6 nanoparticles on two different supports to maximize their dispersion. One high-surface-area carbon support serves as a reference but has limited technological relevance due to its lack of stability. The other support, antimony-doped tin oxide (ATO), has been proposed in the literature as a possible better support for OER catalysts. Temperature-dependent measurements performed in a recently developed gas diffusion electrode (GDE) setup reveal that surprisingly the catalysts immobilized on commercial ATO performed worse than their carbon-immobilized counterparts. The measurements suggest that the ATO support deteriorates particularly fast at elevated temperatures.
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