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作 者:Peiyun Zhou Haokun Pan Guangtong Hai Xiang Liu Xiubing Huang Ge Wang
机构地区:[1]Beijing Advanced Innovation Center for Materials Genome Engineering,Beijing Key Laboratory of Function Materials for Molecule&Structure Construction,School of Materials Science and Engineering,University of Science and Technology Beijing,Beijing 100083,China [2]Department of Chemistry,Tsinghua University,Beijing 100084,China [3]Institute of Zhejiang University-Quzhou,Zhejiang University,Quzhou 324000,Zhejiang,China
出 处:《Journal of Energy Chemistry》2024年第11期721-732,共12页能源化学(英文版)
基 金:National Key Research and Development Program of China (2021YFB3500700);National Natural Science Foundation of China (51802015);Fundamental Research Funds for the Central Universities (FRF-EYIT-23-07)。
摘 要:In this work,nickel foam supported CeO_(2)-modified CoBDC(BDC stands for terephthalic acid linker)metal-organic frameworks(NF/CoBDC@CeO_(2)) are prepared by hydrothermal and subsequent impregnation methods,which can be further transformed to NF/CoOOH@CeO_(2) by reconstruction during the electrocatalytic test.The obtained NF/CoOOH@CeO_(2) exhibits excellent performance in electrocatalytic oxidation of 5-hydroxymethylfurfural(HMF) because the introduction of CeO_(2) can optimize the electronic structure of the heterointerface and accelerate the accumulation of ^(*)OH.It requires only a potential of 1.290 V_(RHE) to provide a current density of 50 mA cm^(-2) in 1.0 M KOH+50 mM HMF,which is 222 mV lower than that required in 1,0 M KOH(1.512 V_(RHE)).In addition,density-functional theory calculation results demonstrate that CeO_(2) biases the electrons to the CoOOH side at the heterointerface and promotes the adsorption of ^(*)OH and ^(*)HMF on the catalyst surface,which lower the reaction energy barrier and facilitate the electrocata lytic oxidation process.
关 键 词:CeO_(2) Metal-organic frameworks 5-Hydroxymethylfurfural oxidation reaction HETEROINTERFACE Reconstruction
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