钴
苯胺
催化作用
双功能
材料科学
纳米颗粒
苯甲醇
甲烷氧化偶联
联轴节(管道)
吸附
组合化学
基质(水族馆)
合理设计
电子转移
双功能催化剂
化学工程
碳纤维
炭黑
偶联反应
纳米技术
光化学
有机化学
氧化磷酸化
作者
Xiaoli Luo,Zhen Liu,Liang Wang,Zhipeng Li,Zhen Wei,Yingzhuang Xu,Junxiao Liu,Weiqin Wei,Yunxiang Li,Shuxin Ouyang,Hong Yuan,Tierui Zhang
标识
DOI:10.1002/adfm.202521413
摘要
Abstract Single‐atom catalysts have been demonstrated promising potential in diverse catalytic reactions; however, their practical application remains hindered by significant limitations in both activity and stability. Therefore, addressing how to effectively enhance their performance remains a critical challenge in the field of single‐atom catalysis. Herein, a Co single‐atom catalyst synergized with Co nanoparticles on a carbon support for oxidative coupling of benzyl alcohol and aniline into N‐benzylideneaniline in an O 2 atmosphere is developed. The catalyst exhibits 95% conversion and 95% selectivity, a remarkable reaction rate enhancement (4 fold increase compared to an individual Co single‐atom catalyst), remarkable stability, and excellent substrate versatility. Furthermore, systematic investigations reveal that Co nanoparticles not only facilitate electron transfer between Co single‐atom sites and O 2 but also serve as an enrichment site for aniline molecules, thereby preventing strong adsorption of aniline onto Co single‐atom sites. These findings provide new insights into the rational design of high‐performance single‐atom catalysts for multi‐step organic transformation through combining with bifunctional nanoparticles.
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