电催化剂
材料科学
Nafion公司
电极
碳纤维
循环伏安法
辅助电极
布基纸
纳米技术
化学工程
X射线光电子能谱
伏安法
碳纳米管
电化学
复合数
复合材料
化学
物理化学
工程类
电解质
作者
Matthew A. Bird,Sean E. Goodwin,Darren A. Walsh
标识
DOI:10.1021/acsami.0c03307
摘要
Screening new electrocatalysts is key to the development of new materials for next-generation energy devices such as fuel cells and electrolyzers. The counter electrodes used in such tests are often made from materials such as Pt and Au, which can dissolve during testing and deposit onto test electrocatalysts, resulting in inaccurate results. The most common strategy for preventing this effect is to separate the counter electrode from the test material using an ion-transporting Nafion membrane. Here, we use X-ray photoelectron spectroscopy, energy-dispersive X-ray analysis, mass spectrometry, and voltammetry to demonstrate the limitations of this approach during constant-current, extended stability testing of electrocatalysts for H2 evolution. We show that Nafion membranes cannot prevent contamination of carbon electrocatalysts by Pt and Au counter electrodes, leading to an apparent increase in the electrocatalytic activity of the carbon. We then demonstrate that carbon counter electrodes in undivided cells can contaminate and deactivate Pt and Au electrocatalysts for H2 evolution. We show that use of a setup composed of a glass frit separating a carbon counter electrode from the test electrocatalyst can prevent these effects. Finally, we discuss these phenomena using H2 evolution at MoS2 and at a K6[P2W18O62](H2O)14/carbon nanotube composite as test reactions.
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