电催化剂
格式化
法拉第效率
催化作用
电化学
电子转移
插层(化学)
材料科学
化学
化学工程
无机化学
光化学
电极
物理化学
有机化学
工程类
作者
Liangping Xiao,Qizheng Zheng,Shiwen Luo,Yifan Ying,Rusen Zhou,Shiyuan Zhou,Xingyun Li,Xiaoyuan Ye,Zhiyang Yu,Qingchi Xu,Hong‐Gang Liao,Jun Xu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-06-19
卷期号:10 (25)
被引量:1
标识
DOI:10.1126/sciadv.adn2707
摘要
Nanoconfined catalysts enhance stabilization of reaction intermediates, facilitate electron transfer, and safeguard active centers, leading to superior electrocatalytic activity, particularly in CO 2 reduction reactions (CO 2 RR). Despite their effectiveness, crafting nanoconfined catalysts is challenging due to unclear formation mechanisms. In this study, we introduce an electrochemical method to grow Pd clusters within the interlayers of two-dimensional black phosphorus, creating Pd cluster–intercalated black phosphorus (Pd-i-BP) as an electrocatalyst. Using in situ electrochemical liquid phase transmission electron microscopy (EC-TEM), we revealed the synthesis mechanism of Pd-i-BP, involving electrochemically driven Pd ion intercalation followed by reduction within the BP layers. The Pd-i-BP electrocatalyst exhibits exemplary CO 2 -to-formate conversion, achieving 90% Faradaic efficiency for formate production, owing to its distinct nanoconfined structure that stabilizes intermediates and enhances electron transfer. Density functional theory (DFT) calculations underscore the structural benefits for enhancing intermediate adsorption and catalyzing the reaction. Our insights deepen understanding of nanoconfined material synthesis, promising advanced, high-efficiency catalysts.
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