Polyacrylate modified Cu electrode for selective electrochemical CO_(2) reduction towards multicarbon products
聚丙烯酸酯修饰铜电极用于电化学二氧化碳还原选择性生成多碳产物作者机构:International Research Center for Renewable EnergyState Key Laboratory of Multiphase Flow in Power EngineeringXi’an Jiaotong UniversityXi’an 710049China Department of PhysicsTamkang UniversityNew Taipei City 25137China
出 版 物:《Science Bulletin》 (科学通报(英文版))
年 卷 期:2024年第69卷第15期
页 面:2395-2404页
核心收录:
学科分类:083002[工学-环境工程] 0830[工学-环境科学与工程(可授工学、理学、农学学位)] 081704[工学-应用化学] 08[工学] 0817[工学-化学工程与技术]
基 金:supported by the National Natural Science Foundation of China(52225606,52488201) the Fundamental Research Funds for the Central Universities The Youth Innovation Team of Shaanxi Universities
主 题:Electrochemical CO_(2)reduction Polymer modification Electron transfer C_(2+)products
摘 要:Highly selective production of value-added multicarbon(C^(2+))products via electrochemical CO_(2) reduction reaction(eCO_(2)RR)on polycrystalline copper(Cu)remains ***,the facile surface modification using poly(α-ethyl cyanoacrylate)(PECA)is presented to greatly enhance the C^(2+)selectivity for eCO_(2)RR over polycrystalline Cu,with Faradaic efficiency(FE)towards C^(2+)products increased from30.1%for the Cu electrode to 72.6%for the obtained Cu-PECA electrode at-1.1 V *** hydrogen electrode(RHE).Given the well-determined FEs towards C^(2+)products,the partial current densities for C^(2+)production could be estimated to be-145.4 mA cm~(-2)for the Cu-PECA electrode at-0.9 V *** in a homemade flow ***-situ spectral characterizations and theoretical calculations reveal that PECA featured with electron-accepting-C≡N and-COOR groups decorated onto the Cu electrode could inhibit the adsorption of^(*)H intermediates and stabilize the^(*)CO intermediates,given the redistributed interfacial electron density and the raised energy level of d-band center(E_(d))of Cu active sites,thus facilitating the C-C coupling and then the C^(2+)selective *** study is believed to be guidable to the modification of electrocatalysts and electrodes with polymers to steer the surface adsorption behaviors of reaction intermediates to realize practical eCO_(2)RR towards value-added C^(2+)products with high activity and selectivity.