A universal strategy for the synthesis of transition metal single atom catalysts toward electrochemical CO2 reduction†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2024-09-25 Epub Date: 2024-09-26 DOI:10.1039/d4cc04213a
Bowen Li , Yan Liang , Yinlong Zhu
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Abstract

Herein, a pyrolysis-induced precursor transformation strategy has been proposed. Using pre-synthesized PDA-M as a precursor, the production of transition metal single atom catalysts (SACs) has been achieved, with compositional flexibility at high metal loadings. In particular, the Ni SAC sample has shown promising CO selectivity when evaluated for the electrochemical CO2 reduction reaction, reaching 29.8 mA cm−2 CO partial current density and 90.3% CO faradaic efficiency at −1.05 V vs. RHE.

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用于电化学二氧化碳还原的过渡金属单原子催化剂的通用合成策略
在此,我们提出了一种热解诱导前驱体转化策略。使用预合成的 PDA-M 作为前驱体,生产出了过渡金属单原子催化剂(SAC),在高金属负载下具有成分灵活性。其中,Ni SAC 样品在电化学二氧化碳还原反应中表现出良好的二氧化碳选择性,在 -1.05 V 对 RHE 条件下,二氧化碳部分电流密度达到 29.8 mA cm-2,二氧化碳远化效率达到 90.3%。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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