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Electric double layer-mediated polarization field for optimizing photogenerated carrier dynamics and thermodynamics

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  • Chengxin Zhou

    (Sichuan Changhong Electronic (Group) Co.; Ltd.)

  • Jian Gao

    (Sichuan Changhong Electronic (Group) Co.; Ltd.
    University of Electronic Science and Technology of China)

  • Yunlong Deng

    (Sichuan Changhong Electronic (Group) Co.; Ltd.)

  • Ming Wang

    (Sichuan Changhong Electronic (Group) Co.; Ltd.)

  • Dan Li

    (Sichuan Changhong Electronic (Group) Co.; Ltd.)

  • Chuan Xia

    (University of Electronic Science and Technology of China)

Abstract

Photocatalytic hydrogen evolution efficiency is limited due to unfavorable carrier dynamics and thermodynamic performance. Here, we propose to introduce electronegative molecules to build an electric double layer (EDL) to generate a polarization field instead of the traditional built-in electric field to improve carrier dynamics, and optimize the thermodynamics by regulating the chemical coordination of surface atoms. Based on theoretical simulation, we designed CuNi@EDL and applied it as the cocatalyst of semiconductor photocatalysts, finally achieved a hydrogen evolution rate of 249.6 mmol h−1 g−1 and remained stable after storing under environmental conditions for more than 300 days. The high H2 yield is mainly due to the perfect work function, Fermi level and Gibbs free energy of hydrogen adsorption, improved light absorption ability, enhanced electron transfer dynamics, decreased HER overpotential and effective carrier transfer channel arose by EDL. Here, our work opens up new perspectives for the design and optimization of photosystems.

Suggested Citation

  • Chengxin Zhou & Jian Gao & Yunlong Deng & Ming Wang & Dan Li & Chuan Xia, 2023. "Electric double layer-mediated polarization field for optimizing photogenerated carrier dynamics and thermodynamics," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38600-8
    DOI: 10.1038/s41467-023-38600-8
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    References listed on IDEAS

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