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作 者:Yuxin Liu Yang Gao Feng He Yurui Xue Yuliang Li
机构地区:[1]Institute of Chemistry,Chinese Academy of Sciences,Beijing 100190 [2]University of Chinese Academy of Sciences,Beijing 100049 [3]Science Center for Material Creation and Energy Conversion,School of Chemistry and Chemical Engineering,Institute of Frontier and Interdisciplinary Science,Shandong University,Jinan 250100
出 处:《CCS Chemistry》2023年第4期971-981,共11页中国化学会会刊(英文)
基 金:by a generous grant from the National Key Research and Development Project of China(no.2018YFA0703501);the National Nature Science Foundation of China(nos.21790050,21790051,and 22021002);the Key Program of the Chinese Academy of Sciences(no.XDPB13).
摘 要:Here we report an in situ assembly growth method that controls the growth of NiTCNQ on the surface of graphdiyne(GDY).The catalytic system of donor–acceptor–donor(GDY/TCNQ/Ni)structure with multiple charge transfer(CT)was achieved by controlling the growth of NiTCNQ on the surface of GDY.Significantly,a controlled double layer interface of GDY/TCNQ/Ni was formed.This system implemented simultaneously the two elements we expected(1)an incomplete CT,and(2)the infinite distribution of active sites originating from highly asymmetric surface charge distribution.The high conductivity and typical semiconductor characteristics of the catalyst endows it with high catalytic activity.We found that an electrolytic cell consisting of the CT salt as a catalyst provided a 1.40 V ultra-small cell voltage up to 10 mA cm−2 and the outer GDY film effectively prevented the corrosion of the catalyst.Our study is the first to introduce CT complexes to a novel catalytic material platform for high selectivity of catalysts,and undoubtedly demonstrates the high selectivity,stability,and activity of such catalytic systems,which provides a new space for the development of novel conceptual catalysts.
关 键 词:graphdiyne charge transfer salts donor-acceptor-donor structure overall water splitting
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