Weakened hydrophobic interactions enhance bubble release in electrocatalytic water-splitting

被引:0
|
作者
Zhang, Zhiqing [1 ]
Qiao, Chenyu [2 ]
Li, Jingqiao [2 ]
Li, Pengcheng [1 ]
Zhang, Hao [2 ]
Liu, Qingxia [2 ,3 ]
Zeng, Hongbo [2 ]
Li, Ge [1 ]
机构
[1] Univ Alberta, Dept Mech Engn, Edmonton, AB T6G 1H9, Canada
[2] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 1H9, Canada
[3] Shenzhen Technol Univ, Future Technol Sch, Shenzhen 518118, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
Superaerophobic; Electrode-bubble interactions; Three-phase interface; Water-splitting; AIR BUBBLES; EVOLUTION; SURFACES; FORCES; FILMS;
D O I
10.1016/j.apcatb.2025.125019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In scaling up electrocatalytic water-splitting processes, a key challenge is the inherent sluggishness resulting from bubble adhering to electrode and associated interfacial interactions at electrode-electrolyte interface. Therefore, we address this issue by modifying microenvironment at electrode-electrolyte interface, where we developed superaerophobic CoP (a representative electrocatalyst) that effectively mitigated the bubble-related problem. To elucidate underlying mechanisms of bubble release process, we systematic investigated the interaction forces between different CoP surfaces and bubbles using direct force measurements coupled with theoretical calculation. The van der Waals (VDW) and electric double layer (EDL) forces were found to be always repulsive regardless of changes in the microenvironment, and the attractive hydrophobic (HB) interaction dominated the behavior of gas bubbles (attachment or detachment) at the electrode surface during water-splitting. Enhanced superaerophobicity of our CoP stems from weakened HB attraction between the electrode and bubbles, leading to faster bubble release and facilitated interfacial mass transfer. Our finding improves the fundamental understanding of bubble dynamics in gas evolution process and provides a strategy for optimizing the performance of electrocatalysts.
引用
收藏
页数:10
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