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Bifunctional ionomers for efficient co-electrolysis of CO2 and pure water towards ethylene production at industrial-scale current densities

Author

Listed:
  • Wenzheng Li

    (Wuhan University)

  • Zhenglei Yin

    (Wuhan University)

  • Zeyu Gao

    (Wuhan University)

  • Gongwei Wang

    (Wuhan University)

  • Zhen Li

    (Wuhan University)

  • Fengyuan Wei

    (Wuhan University)

  • Xing Wei

    (Wuhan University)

  • Hanqing Peng

    (Wuhan University)

  • Xingtao Hu

    (Wuhan University)

  • Li Xiao

    (Wuhan University)

  • Juntao Lu

    (Wuhan University)

  • Lin Zhuang

    (Wuhan University
    Wuhan University)

Abstract

Many CO2 electrolysers under development use liquid electrolytes (KOH solutions, for example), yet using solid-state polymer electrolytes can in principle improve efficiency and realize co-electrolysis of CO2 and pure water, avoiding corrosion and electrolyte consumption issues. However, a key challenge in these systems is how to favour production of multicarbon molecules, such as ethylene, which typically necessitates a strong alkaline environment. Here we use bifunctional ionomers as polymer electrolytes that are not only ionically conductive but can also activate CO2 at the catalyst–electrolyte interface and favour ethylene synthesis, while running on pure water. Specifically, we use quaternary ammonia poly(ether ether ketone) (QAPEEK), which contains carbonyl groups in the polymer chain, as the bifunctional electrolyte. An electrolyser running on CO2 and pure water exhibits a total current density of 1,000 mA cm−2 at cell voltages as low as 3.73 V. At 3.54 V, ethylene is produced with the industrial-scale partial current density of 420 mA cm−2 without any electrolyte consumption.

Suggested Citation

  • Wenzheng Li & Zhenglei Yin & Zeyu Gao & Gongwei Wang & Zhen Li & Fengyuan Wei & Xing Wei & Hanqing Peng & Xingtao Hu & Li Xiao & Juntao Lu & Lin Zhuang, 2022. "Bifunctional ionomers for efficient co-electrolysis of CO2 and pure water towards ethylene production at industrial-scale current densities," Nature Energy, Nature, vol. 7(9), pages 835-843, September.
  • Handle: RePEc:nat:natene:v:7:y:2022:i:9:d:10.1038_s41560-022-01092-9
    DOI: 10.1038/s41560-022-01092-9
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    Cited by:

    1. Yinchao Yao & Tong Shi & Wenxing Chen & Jiehua Wu & Yunying Fan & Yichun Liu & Liang Cao & Zhuo Chen, 2024. "A surface strategy boosting the ethylene selectivity for CO2 reduction and in situ mechanistic insights," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    2. Xiaojie She & Lingling Zhai & Yifei Wang & Pei Xiong & Molly Meng-Jung Li & Tai-Sing Wu & Man Chung Wong & Xuyun Guo & Zhihang Xu & Huaming Li & Hui Xu & Ye Zhu & Shik Chi Edman Tsang & Shu Ping Lau, 2024. "Pure-water-fed, electrocatalytic CO2 reduction to ethylene beyond 1,000 h stability at 10 A," Nature Energy, Nature, vol. 9(1), pages 81-91, January.

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