电解质
乙烯
化学工程
气体扩散
碳酸乙烯酯
电极
催化作用
扩散
化学
电解
膜电极组件
材料科学
有机化学
物理化学
工程类
物理
热力学
作者
Linbo Li,Xiaolong Zhang,Chuangwei Liu,Venkata Sai Sriram Mosali,Jun Chen,Alan M. Bond,Qinfen Gu,Jie Zhang
标识
DOI:10.1016/j.apcatb.2023.122597
摘要
Electroreduction using a gas diffusion electrode (GDE) provides an efficient method for high rate conversion of CO2 to value-added chemicals. However, long term production with high yields remains challenging due to rapid electrolyte flooding through the hydrophobic gas diffusion layer (GDL). Here, we report a universal strategy to convert a commercial GDL into a hydrophobicity graded GDL (HGGDL) that resists electrolyte flooding. The CO2 electroreduction performance of a family of tandem catalysts consisting of a nickel-single-atom catalyst and Cu nanoparticles immobilized on GDLs and HGGDLs is compared with respect to ethylene production. In situ Raman studies reveal that the HGGDL increases the CO intermediate coverage as a result of the higher differential pressure across the electrodes. Lower carbonate formation also is observed. Enhanced ethylene production efficiency and an order of magnitude improvement in long term stability is achieved in a membrane electrode assembly electrolyzer.
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