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Integrating hydrogen utilization in CO2 electrolysis with reduced energy loss

Author

Listed:
  • Xiaoyi Jiang

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

  • Le Ke

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

  • Kai Zhao

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

  • Xiaoyu Yan

    (Wuhan University)

  • Hongbo Wang

    (Wuhan University)

  • Xiaojuan Cao

    (Wuhan University)

  • Yuchen Liu

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

  • Lingjiao Li

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

  • Yifei Sun

    (Shenzhen Research Institute of Xiamen University)

  • Zhiping Wang

    (Wuhan University)

  • Dai Dang

    (Guangdong University of Technology)

  • Ning Yan

    (Wuhan University
    Shenzhen Research Institute of Wuhan University)

Abstract

Electrochemical carbon dioxide reduction reaction using sustainable energy is a promising approach of synthesizing chemicals and fuels, yet is highly energy intensive. The oxygen evolution reaction is particularly problematic, which is kinetically sluggish and causes anodic carbon loss. In this context, we couple CO2 electrolysis with hydrogen oxidation reaction in a single electrochemical cell. A Ni(OH)2/NiOOH mediator is used to fully suppress the anodic carbon loss and hydrogen oxidation catalyst poisoning by migrated reaction products. This cell is highly flexible in producing either gaseous (CO) or soluble (formate) products with high selectivity (up to 95.3%) and stability (>100 h) at voltages below 0.9 V (50 mA cm−2). Importantly, thanks to the “transferred” oxygen evolution reaction to a water electrolyzer with thermodynamically and kinetically favored reaction conditions, the total polarization loss and energy consumption of our H2-integrated CO2 reduction reaction, including those for hydrogen generation, are reduced up to 22% and 42%, respectively. This work demonstrates the opportunity of combining CO2 electrolysis with the hydrogen economy, paving the way to the possible integration of various emerging energy conversion and storage approaches for improved energy/cost effectiveness.

Suggested Citation

  • Xiaoyi Jiang & Le Ke & Kai Zhao & Xiaoyu Yan & Hongbo Wang & Xiaojuan Cao & Yuchen Liu & Lingjiao Li & Yifei Sun & Zhiping Wang & Dai Dang & Ning Yan, 2024. "Integrating hydrogen utilization in CO2 electrolysis with reduced energy loss," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-45787-x
    DOI: 10.1038/s41467-024-45787-x
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    References listed on IDEAS

    as
    1. Ke Xie & Adnan Ozden & Rui Kai Miao & Yuhang Li & David Sinton & Edward H. Sargent, 2022. "Eliminating the need for anodic gas separation in CO2 electroreduction systems via liquid-to-liquid anodic upgrading," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Miao Zhong & Kevin Tran & Yimeng Min & Chuanhao Wang & Ziyun Wang & Cao-Thang Dinh & Phil De Luna & Zongqian Yu & Armin Sedighian Rasouli & Peter Brodersen & Song Sun & Oleksandr Voznyy & Chih-Shan Ta, 2020. "Accelerated discovery of CO2 electrocatalysts using active machine learning," Nature, Nature, vol. 581(7807), pages 178-183, May.
    3. Sumit Verma & Shawn Lu & Paul J. A. Kenis, 2019. "Co-electrolysis of CO2 and glycerol as a pathway to carbon chemicals with improved technoeconomics due to low electricity consumption," Nature Energy, Nature, vol. 4(6), pages 466-474, June.
    4. Haeun Shin & Kentaro U. Hansen & Feng Jiao, 2021. "Techno-economic assessment of low-temperature carbon dioxide electrolysis," Nature Sustainability, Nature, vol. 4(10), pages 911-919, October.
    5. Jonggeol Na & Bora Seo & Jeongnam Kim & Chan Woo Lee & Hyunjoo Lee & Yun Jeong Hwang & Byoung Koun Min & Dong Ki Lee & Hyung-Suk Oh & Ung Lee, 2019. "General technoeconomic analysis for electrochemical coproduction coupling carbon dioxide reduction with organic oxidation," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
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