材料科学
电极
纳米技术
纳米-
电化学
Boosting(机器学习)
纳米尺度
气体扩散
化学工程
复合材料
化学
物理化学
机器学习
计算机科学
工程类
作者
Zhe Jiang,Zhen‐Hua Lyu,Xiaozhi Liu,Jiaju Fu,Li‐Bing Zhang,Ze‐Cheng Yao,Lirong Zheng,Dong Su,Youjun Fan,Tang Tang,Jin‐Song Hu
标识
DOI:10.1002/adfm.202401927
摘要
Abstract Electrochemical flow cells based on gas diffusion electrodes (GDEs) provide a potential means to achieve industrial‐compatible massive CO production. However, the application of flow cells is hindered by the stability issue caused by GDE hydrophilizing and electrolyte flooding. The current strategies have certain limitations in maintaining the long‐term hydrophobicity of GDE. Inspired by the superhydrophobic materials in nature, here a constructionally engineered superhydrophobic GDE is presented for boosting the stability of CO 2 reduction to CO in flow cells under industrial‐compatible current densities. This superhydrophobic GDE is comprised of micro/nano‐structured CNTs/graphene composites with abundant and robust single‐atomic Ni‐N x active sites (Ni SA ‐CNT@G). The unique integrated hierarchical structure with highly exposed surface area and enhanced mass/charge transfer contributes to an industrial‐scale CO partial current density of 406.5 mA cm −2 with a FE CO of 96.3% in a flow cell . Notably, the robust superhydrophobic micro/nanostructure efficiently resists electrolyte flooding over the GDE during the CO 2 RR, thus maintaining a stable three‐phase interface. Over 70 h stability is demonstrated at an industrial‐compatible current density of 300 mA cm −2 . These results open up new opportunities for industrial‐level CO production via electrochemical CO 2 RR.
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