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Wien effect in interfacial water dissociation through proton-permeable graphene electrodes

Author

Listed:
  • J. Cai

    (The University of Manchester
    The University of Manchester
    National University of Defense Technology)

  • E. Griffin

    (The University of Manchester
    The University of Manchester)

  • V. H. Guarochico-Moreira

    (The University of Manchester
    The University of Manchester
    Facultad de Ciencias Naturales y Matemáticas)

  • D. Barry

    (The University of Manchester)

  • B. Xin

    (The University of Manchester
    The University of Manchester)

  • M. Yagmurcukardes

    (Universiteit Antwerpen
    Izmir Institute of Technology)

  • S. Zhang

    (Tianjin University)

  • A. K. Geim

    (The University of Manchester
    The University of Manchester
    National University of Singapore)

  • F. M. Peeters

    (Universiteit Antwerpen)

  • M. Lozada-Hidalgo

    (The University of Manchester
    The University of Manchester)

Abstract

Strong electric fields can accelerate molecular dissociation reactions. The phenomenon known as the Wien effect was previously observed using high-voltage electrolysis cells that produced fields of about 107 V m−1, sufficient to accelerate the dissociation of weakly bound molecules (e.g., organics and weak electrolytes). The observation of the Wien effect for the common case of water dissociation (H2O $$\leftrightarrows$$ ⇆ H+ + OH−) has remained elusive. Here we study the dissociation of interfacial water adjacent to proton-permeable graphene electrodes and observe strong acceleration of the reaction in fields reaching above 108 V m−1. The use of graphene electrodes allows measuring the proton currents arising exclusively from the dissociation of interfacial water, while the electric field driving the reaction is monitored through the carrier density induced in graphene by the same field. The observed exponential increase in proton currents is in quantitative agreement with Onsager’s theory. Our results also demonstrate that graphene electrodes can be valuable for the investigation of various interfacial phenomena involving proton transport.

Suggested Citation

  • J. Cai & E. Griffin & V. H. Guarochico-Moreira & D. Barry & B. Xin & M. Yagmurcukardes & S. Zhang & A. K. Geim & F. M. Peeters & M. Lozada-Hidalgo, 2022. "Wien effect in interfacial water dissociation through proton-permeable graphene electrodes," Nature Communications, Nature, vol. 13(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33451-1
    DOI: 10.1038/s41467-022-33451-1
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    References listed on IDEAS

    as
    1. Kailong Hu & Tatsuhiko Ohto & Yuki Nagata & Mitsuru Wakisaka & Yoshitaka Aoki & Jun-ichi Fujita & Yoshikazu Ito, 2021. "Catalytic activity of graphene-covered non-noble metals governed by proton penetration in electrochemical hydrogen evolution reaction," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
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    Cited by:

    1. Eli Hoenig & Yu Han & Kangli Xu & Jingyi Li & Mingzhan Wang & Chong Liu, 2024. "In situ generation of (sub) nanometer pores in MoS2 membranes for ion-selective transport," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    2. S. Huang & E. Griffin & J. Cai & B. Xin & J. Tong & Y. Fu & V. Kravets & F. M. Peeters & M. Lozada-Hidalgo, 2023. "Gate-controlled suppression of light-driven proton transport through graphene electrodes," Nature Communications, Nature, vol. 14(1), pages 1-7, December.

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