Bingqing Xu , Israr Masood Ul Hasan , Luwei Peng , Junyu Liu , Nengneng Xu , Mengyang Fan , Nabeel Khan Niazi , Jinli Qiao
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引用次数: 12
Abstract
The conversion of carbon dioxide (CO2) into high-value added energy fuels and chemicals (CO, formate, C2H4, etc.) through electrochemical reduction (eCO2R) is a promising avenue to sustainable development. However, low selectivity, barren activity and poor stability of the electrodes hinder the large-scale application of eCO2R. Herein, we reported a copper-indium-organic-framework (CuIn-MOF) based high-performance catalyst for eCO2R. Electrochemical measurement results reveal that CuIn-MOF exhibits high Faradaic efficiency (FE) of CO and formate (300 mV, FECO = 78.6% at −0.86 V vs. RHE, FEHCOO− = 48.4% at −1.16 V vs. RHE, respectively) in a broad range of current density (20.1–88.4 mA cm−2) with long-term stability (6 h) for eCO2R in 0.5 M KHCO3 electrolyte solution. Specifically, through anion-regulation engineering, SO42− anion precursor is more beneficial for the formic acid generation than NO3− anion precursor; while for SO42− anion precursor, Cu plays a positive regulating role in eCO2R to CO compared to In. Additionally, the high performance in a home-made eCO2R reactor derives benefit from enhanced intrinsic activity and charge re-distribution can be attributed to the formation of In-doped Cu layer.
通过电化学还原(eCO2R)将二氧化碳(CO2)转化为高附加值的能源燃料和化学品(CO、甲酸酯、C2H4等)是一种有前途的可持续发展途径。但其选择性低、活性差、稳定性差等缺点阻碍了eCO2R的大规模应用。在此,我们报道了一种基于铜铟有机框架(cu - mof)的高性能eCO2R催化剂。电化学测量结果表明,cu - mof在电流密度范围(20.1 ~ 88.4 mA cm−2)内具有较高的CO和甲酸的法拉第效率(FE)(−0.86 V vs. RHE时FECO = 78.6%,−1.16 V vs. RHE时FEHCOO = 48.4%),且在0.5 M KHCO3电解质溶液中eCO2R的长期稳定性(6 h)。具体来说,通过阴离子调控工程,SO42−阴离子前体比NO3−阴离子前体更有利于甲酸的生成;而对于SO42−阴离子前驱体,Cu比in在eCO2R到CO中起正向调节作用。此外,国产eCO2R反应器的高性能得益于增强的本征活性和电荷再分配,这可归因于in -掺杂Cu层的形成。