Diminishing Performance of Pt/CNT in Ethanol Oxidation after High-Potential Scanning
Fengping Hu,
Jinchang Xu,
Lin Wei,
Zhenyou Wang,
Fangming Jiang
Affiliations
Fengping Hu
Laboratory of Advanced Energy Systems, CAS Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences (CAS), Guangzhou 510640, China
Jinchang Xu
Guangdong Provincial Key Laboratory of Terahertz Quantum Electromagnetics, GBA Branch of Aerospace Information Research Institute, Chinese Academy of Sciences (CAS), Guangzhou 510700, China
Lin Wei
Laboratory of Advanced Energy Systems, CAS Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences (CAS), Guangzhou 510640, China
Zhenyou Wang
Guangdong Provincial Key Laboratory of Terahertz Quantum Electromagnetics, GBA Branch of Aerospace Information Research Institute, Chinese Academy of Sciences (CAS), Guangzhou 510700, China
Fangming Jiang
Laboratory of Advanced Energy Systems, CAS Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences (CAS), Guangzhou 510640, China
Regenerative fuel cells and the phenomenon of cell reversal (CR) necessitate creating robust catalyst layers for consistent performance in fuel cells. This research used in situ Raman spectroscopy to observe molecular alterations on carbon nanotube-supported platinum catalysts (Pt/CNT) during ethanol oxidation. Following a CR event simulation, the ethanol oxidation efficiency on Pt/CNT was amplified 2.8 times after high-potential scanning but reverted to its initial efficiency after 100 cycles. The adsorbed *CO2− species on Pt/CNT was pivotal for initiating ethanol oxidation, with the rate assessed through Raman analysis. In addition to water electrolysis, the carbon substrate was degraded. This study sheds light on the mechanisms behind catalyst degradation, steering the creation of more advanced catalysts.
