Monteiro Mariana C O, Jacobse Leon, Koper Marc T M
Leiden Institute of Chemistry, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.
DESY NanoLab, Deutsches Elektronensynchrotron DESY, Notkestrasse 85, D-22607 Hamburg, Germany.
J Phys Chem Lett. 2020 Nov 19;11(22):9708-9713. doi: 10.1021/acs.jpclett.0c02779. Epub 2020 Nov 2.
Recently, the bulk electrooxidation of CO on gold or platinum has been used to detect CO produced during CO reduction in neutral media. The CO bulk oxidation voltammetry may show two distinct peaks depending on the reaction conditions, which up to now have not been understood. We have used scanning electrochemical microscopy (SECM) to probe CO oxidation and pH in the diffusion layer during CO reduction. Our results show that the two different peaks are due to diffusion limitation by two different species, namely, CO and OH. We find that between pH 7 and 11, CO oxidation by water and OH gives rise to the first and second peak observed in the voltammetry, respectively. Additional rotating disc experiments showed that specifically in this pH range the current of the second peak is diffusion limited by the OH concentration, since it is lower than the CO concentration.
最近,金或铂上一氧化碳的体相电氧化已被用于检测中性介质中一氧化碳还原过程中产生的一氧化碳。根据反应条件,一氧化碳体相氧化伏安法可能会显示出两个不同的峰,到目前为止这一点尚未得到理解。我们使用扫描电化学显微镜(SECM)来探测一氧化碳还原过程中扩散层内的一氧化碳氧化和pH值。我们的结果表明,这两个不同的峰是由两种不同物质的扩散限制导致的,即一氧化碳和氢氧根。我们发现,在pH值7到11之间,水和氢氧根对一氧化碳的氧化分别产生了伏安法中观察到的第一个和第二个峰。额外的旋转圆盘实验表明,特别是在这个pH范围内,第二个峰的电流受氢氧根浓度的扩散限制,因为它低于一氧化碳浓度。