Liu Yan, Zheng Yamin, Dong Panpan, Zhang Wenzhuang, Wu Wenjie, Mao Junjie
Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, China.
Institute of Chemistry, the Chinese Academy of Sciences (CAS), Beijing 100190, China.
ACS Appl Mater Interfaces. 2021 Dec 29;13(51):61047-61054. doi: 10.1021/acsami.1c17205. Epub 2021 Dec 14.
Development of high-performance heterogeneous catalytic materials is important for the rapid upgrade of chemicals, which remains a challenge. Here, the benzene oxidation reaction was used to demonstrate the effectiveness of the atomic interface strategy to improve catalytic performance. The developed B,N-cocoordinated Cu single atoms anchored on carbon nanosheets (Cu/B-N) with the Cu-NB atomic interface was prepared by the pyrolysis of a precoordinated Cu precursor. Benefiting from the unique atomic Cu-NB interfacial structure, the designed Cu/B-N exhibited considerable activity in the oxidation of benzene, which was much higher than Cu/N-C, Cu NPs/N-C, and N-C catalysts. A theoretical study showed that the enhanced catalytic performance resulted from the optimized adsorption of intermediates, which originated from the manipulation of the electronic structure of Cu single atoms induced by B atom coordination in the Cu-NB atomic interface. This study provides an innovative approach for the rational design of high-performance heterogeneous catalytic materials at the atomic level.
开发高性能多相催化材料对于化学品的快速升级很重要,但这仍然是一个挑战。在此,通过苯氧化反应来证明原子界面策略在提高催化性能方面的有效性。通过对预配位铜前驱体进行热解,制备出了具有Cu-NB原子界面、B,N共配位的铜单原子锚定在碳纳米片上的材料(Cu/B-N)。得益于独特的原子Cu-NB界面结构,所设计的Cu/B-N在苯氧化反应中表现出相当高的活性,远高于Cu/N-C、Cu NPs/N-C和N-C催化剂。理论研究表明,催化性能的增强源于中间体吸附的优化,这源于Cu-NB原子界面中B原子配位对铜单原子电子结构的调控。该研究为在原子水平上合理设计高性能多相催化材料提供了一种创新方法。