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作 者:Yuqi Ren Hongxu Zhang Caihong Hao Qing Chang Ning Li Jinlong Yang Shengliang Hu
机构地区:[1]Research Group of New Energy Materials and Devices,North University of China,Taiyuan 030051,China [2]State Key Laboratory of New Ceramics and Fine Processing,Tsinghua University,Beijing 100084,China
出 处:《Chinese Chemical Letters》2024年第1期332-337,共6页中国化学快报(英文版)
基 金:Fundamental Research Program of Shanxi Province of China(No.20210302123037);Research Project Supported by Shanxi Scholarship Council of China(No.2022-136);Specialized Research Fund for Sanjin Scholars Program of Shanxi Province of China.
摘 要:The chemoselective hydrogenation of structurally diverse nitroaromatics is a challenging process.Generally,catalyst activity tends to decrease when excellent selectivity is guaranteed.We here present a novel photocatalyst combining amino-functionalized carbon dots(N-CDs)with copper selenite nanoparticles(N-CDs@CuSeO_(3))for simultaneously improving selectivity and activity.Under visible light irradiation,the prepared N-CDs@CuSeO_(3)exhibits 100%catalytic selectivity for the formation of 4-aminostyrene at full conversion of 4-nitrostyrene in aqueous solvent within a few minutes.Such excellent photocatalytic performance is mainly attributed to the precise control of the hydrogen species released from the ammonia borane by means of light-converted electrons upon N-CDs@CuSeO_(3).Besides,the defect states at the interface of N-CDs and CuSeO_(3)enable holes to be trapped for promoting separation and transfer of photogenerated charges,allowing more hydrogen species to participate in catalytic reaction.
关 键 词:HETEROSTRUCTURE Carbon dots PHOTOCATALYSIS Chemoselective hydrogenation Copper selenite
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