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In situ reversible underwater superwetting transition by electrochemical atomic alternation

Author

Listed:
  • Qianbin Wang

    (Beihang University)

  • Bojie Xu

    (Beihang University)

  • Qing Hao

    (Chinese Academy of Sciences)

  • Dong Wang

    (Chinese Academy of Sciences)

  • Huan Liu

    (Beihang University)

  • Lei Jiang

    (Beihang University
    Chinese Academy of Sciences)

Abstract

Materials with in situ reversible wettability have attractive properties but remain a challenge to use since the inverse process of liquid spreading is normally energetically unfavorable. Here, we propose a general electrochemical strategy that enables the in situ reversible superwetting transition between underwater superoleophilicity and superoleophobicity by constructing a binary textured surface. Taking the copper/tin system as an example, the surface energy of the copper electrode can be lowered significantly by electrodeposited tin, and be brought back to the initial high-energy state as a result of dissolving tin by removing the potential. Tin atoms with the water depletion layer inhibit the formation of a hydrogen-bonding network, causing oil droplets to spread over the surface, while copper atoms, with a high affinity for hydroxyl groups, facilitate replacing the oil layer with the aqueous electrolyte. The concept is applicable to other systems, such as copper/lead, copper/antimony, gold/tin, gold/lead and gold/antimony, for both polar and nonpolar oils, representing a potentially useful class of switchable surfaces.

Suggested Citation

  • Qianbin Wang & Bojie Xu & Qing Hao & Dong Wang & Huan Liu & Lei Jiang, 2019. "In situ reversible underwater superwetting transition by electrochemical atomic alternation," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09201-1
    DOI: 10.1038/s41467-019-09201-1
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