气泡
微尺度化学
聚结(物理)
化学物理
传质
毫秒
机械
超微电极
动力学(音乐)
纳米技术
材料科学
时间分辨率
液体气泡
电化学
电流(流体)
化学
传热
浮力
作者
Yunli Zhou,Jiaxin Feng,Jincan Pei,Canjun Liu,Jie Zhang,Zhangquan Peng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-19
卷期号:19 (38): 34080-34088
被引量:7
标识
DOI:10.1021/acsnano.5c10124
摘要
Bubble engineering enhances mass transfer in electrochemical gas-evolution devices by accelerating bubble detachment. Understanding dynamics from single-bubble growth to microscale bubble–bubble interactions is fundamental to bubble engineering but remains challenging. Herein, by integrating ultramicroelectrode electrochemistry with high-speed dark-field microscopy, we correlate electrochemical responses to bubble dynamics with synchronized optical signals, revealing dynamics beyond the single-bubble regime at millisecond temporal resolution and microscale spatial resolution. At the single-bubble level, position-dependent growth dynamics (edge vs center) of O 2 bubbles generated during water electrolysis are characterized. An electrochemical method quantifies contact angles using residual current ratios and bubble diameters, revealing superior aerophobicity (θ ≈ 170°) of electrogenerated Ni(OH) 2 surfaces. Crucially, beyond the single-bubble regime, we decipher electrode–bubble interactions and bubble–bubble interactions by prepositioning an O 2 bubble adjacent to the electrode. Electrode–bubble interactions reveal electrochemically driven growth of a neighboring bubble and ∼30% enhancement of local mass transfer. Bubble–bubble interactions demonstrate coalescence-induced recovery of bubble-blocked current within ∼4 ms via accelerated detachment. These results highlight interactions transcending the single-bubble regime, specifically pairwise bubble interactions, and establish a mechanistic framework of counteract-bubbles-with-bubbles strategy for macroscopic bubble engineering. This strategy is expected to promote the structural design of practical gas-evolution devices with minimized mass transfer resistance.
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