高电位扫描增强Pt/C和Pd/C催化剂乙醇氧化性能的原位拉曼光谱研究

IF 4.7 3区 工程技术 Q2 ELECTROCHEMISTRY Electrochemistry Communications Pub Date : 2023-09-01 DOI:10.1016/j.elecom.2023.107561
Fengping Hu , Jinchang Xu , Lin Wei , Zhenyou Wang , Fangming Jiang
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引用次数: 0

摘要

乙醇氧化(EOR)的高效催化对能源转换和储存技术的发展具有至关重要的意义。利用高电位扫描技术研究了J-M Pt/C和Pd/C催化剂对乙醇氧化的催化性能。利用原位拉曼光谱对电化学反应中的中间体进行了分析。我们的研究结果表明,Pd/C催化剂的催化活性和稳定性显著增强,这可能归因于Pd/C电极上的高电位活化。有趣的是,在相同的实验条件下,Pt/C和Pd/C催化剂的反应结果不同。本研究为设计和开发高效的乙醇氧化催化剂提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In situ Raman study of high potential scan enhanced Pt/C and Pd/C catalyst performance for ethanol oxidation

The efficient catalysis of ethanol oxidation (EOR) is of paramount importance for the progress of energy conversion and storage technologies. We investigate the improved catalytic performance of commercial J-M Pt/C and Pd/C catalysts for ethanol oxidation by utilizing high potential scanning. By employing in situ Raman spectroscopy, we analyze the reaction intermediates during electrochemical reactions. Our findings highlight that the Pd/C catalyst exhibits remarkable enhancements in catalytic activity and stability, which can be attributed to the activation at high potentials on Pd/C electrode. Interestingly, different results are observed between Pt/C and Pd/C catalysts under the same experimental conditions. This study provides valuable insights into the design and development of efficient catalysts for ethanol oxidation.

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来源期刊
Electrochemistry Communications
Electrochemistry Communications 工程技术-电化学
CiteScore
8.50
自引率
3.70%
发文量
160
审稿时长
1.2 months
期刊介绍: Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.
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