界面和价态对提高 La2CuO4 的电化学二氧化碳还原活性的协同效应

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Shiya Bian , Xuekun Jin , Jinxing Mi , Fengjuan Chen , Li Cai , Ziyu Wang , Junhua Li , Jianjun Chen
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引用次数: 0

摘要

电化学二氧化碳还原反应(CER)转化为甲烷(CH4)受到了极大关注。在此,我们提出了一种有效的方法,通过在脲修饰的 La2CuO4 催化剂上创建两相界面来促进 CO2 到 CH4 的转化。最优化的催化剂对 CH4 的选择性最高(22%),在与可逆氢电极相比-1 V 的电位下,活性(14 mA cm-2)和稳定性(5 h)最佳。CER 性能的提高可归因于两相内界面效应的建立,这有利于 Cu2+ 的还原并促进活性位点的富集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4

Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4

Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4

The electrochemical CO2 reduction reaction (CER) to methane (CH4) has received great attention. Here, we proposed an efficient method to facilitate the conversion of CO2-to-CH4 by creating a two-phase interface over urea-modified La2CuO4 catalyst. The most optimized one exhibits the highest selectivity (22%) for CH4 and the best activity (14 mA cm−2) and stability (5 h) at the potential of −1 V vs. reversible hydrogen electrode. The enhanced CER performance can be attributed to the establishment of interfacial effect within the two-phase, which facilitates the reduction of Cu2+ and promotes the active sites concentration.

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来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
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