材料科学
催化作用
电催化剂
星团(航天器)
煅烧
原位
法拉第效率
金属
Atom(片上系统)
产量(工程)
化学工程
纳米技术
化学物理
过渡金属
协同催化
X射线光电子能谱
多孔性
氧还原反应
无机化学
能量转换
作者
Jian Wei,Qian Bai,Chen Li,Dengyu Chen,Zhiyi Sun,Huan Wang,Kun Zheng,Zihao Wei,Huishan Shang,Wenxing Chen
标识
DOI:10.1002/adfm.202525281
摘要
Abstract Fully exposed atomically dispersed metal cluster (ACs) catalysts offer near‐100% atom utilization and exceptional catalytic activity, yet achieving high loading and controlled synthesis remains challenging. To address this issue, leveraging high‐temperature calcination of porous C 2 N and its inherent 2D confinement effect, asymmetric 3d metal clusters are in situ anchored within cavity centers (asymmetric MACs/C 2 N), yielding high‐loading (12.8 wt.%), fully exposed asymmetric Cu ACs. For the model nitrate reduction (NO 3 RR), CuACs/C 2 N exhibit exceptional catalytic performance, achieving a Faradaic efficiency of 97.9% and an NH 3 yield of 0.66 mg h −1 cm −2 at −0.6 V. Spectroscopic analysis and theoretical calculations indicate that the dynamic evolution of the asymmetric Cu 5 N 2 active sites during the reaction significantly lowers the reaction energy barrier. This strategy is further applicable to 4d palladium‐ and 5d platinum‐based systems (PdACs/C 2 N, PtACs/C 2 N), demonstrating its broad potential. The development of high‐loading asymmetric atomic clusters offers a novel and effective approach for constructing highly active catalytic sites in advanced electrocatalysts.
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