Real-time monitoring of electrochemical carbon corrosion in alkaline media

被引:30
|
作者
Ji, Sang Gu [1 ]
Kim, Haesol [1 ]
Lee, Woong Hee [2 ]
Oh, Hyung-Suk [2 ]
Choi, Chang Hyuck [1 ]
机构
[1] Gwangju Inst Sci & Technol GIST, Sch Mat Sci & Engn, Gwangju 61005, South Korea
[2] Korea Inst Sci & Technol KIST, Clean Energy Res Ctr, Hwarang Ro 14,Gil 5, Seoul 02792, South Korea
基金
新加坡国家研究基金会;
关键词
PT/C CATALYSTS; OXYGEN REDUCTION; GLASSY-CARBON; FUEL-CELLS; SUPPORT; ELECTROCATALYSTS; DEGRADATION; PLATINUM; ELECTRODES; BEHAVIOR;
D O I
10.1039/d1ta01748a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon materials have been used as supporting substrates for electrocatalytically active species in many important reactions due to their high electrical conductivity and chemical inertness. To secure durable electrocatalysis, the fundamental understanding and prevention of corrosion are pivotal. The real-time monitoring of evolved CO2 enabled by differential electrochemical mass spectroscopy (DEMS) has provided potential-resolved information about carbon corrosion. However, this approach is typically limited to acidic media and it is unavailable in alkaline media because of the carbonation of the CO2 tracer. In this study, we investigate carbon corrosion using carbon monoxide (CO) as a corrosion marker. The electrochemical oxidation of selected model substrates (i.e., activated carbon, graphite, and Pt/C) is analyzed under dynamic and static potential excursions using DEMS. The results demonstrate that the CO tracer successfully monitored carbon corrosion in both acidic and alkaline media. The corrosion in alkaline media is qualitatively analogous to that in acidic media, but it is quantitatively alleviated, as confirmed by the decreased DEMS intensity and the decreased faradaic charge flowed.
引用
收藏
页码:19834 / 19839
页数:6
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