析氧
气泡
化学物理
成核
离聚物
氧气
纳米技术
材料科学
时间演化
化学
电极
分子
电流(流体)
相(物质)
电解
大规模运输
液体气泡
电解水
电化学
气相
布里格斯-劳舍尔反应
充氧
氧气输送
直线(几何图形)
作者
Congfan Zhao,Yuan Shu,Jiabin You,Chenyun Bai,Yongjian Su,Xiaojing Cheng,Shuiyun Shen,Xiaohui Yan,Junliang Zhang
标识
DOI:10.1073/pnas.2606452123
摘要
In the oxygen evolution reaction (OER), adherent gas bubbles are conventionally viewed as a major impediment that blocks ion and mass transport by covering active sites. Here, we show that for ionomer-based electrodes, this prevailing view is oversimplified. Using a self-developed transparent on-chip electrolyzer that integrates multimodal in-situ characterization, including optical microscopy, spectroscopic analysis, and atomic force microscopy, we uncover complex intrabubble dynamics on ionomer-coated electrodes. During bubble growth, the three-phase contact line exhibits characteristic pinning-depinning behavior. Beyond a critical bubble size (~420 μm), free water molecules are evolved from the ionomer into the bubble-electrode contact area, forming microdroplets (<20 μm) that continuously coalesce. Inside these microdroplets, oxygen products further nucleate as pancake-shaped nanobubbles (~50 nm), revealing a previously unrecognized intrabubble process. We find that this coupled microdroplet-nanobubble evolution is enabled by the phase-separation behavior of ionomer. The ionomer also preserves local electrochemical activity even under substantial bubble coverage, unlike ionomer-free electrodes where bubble blockage leads to severe deactivation. By tailoring ionomer phase separation, we achieve intensified microdroplet-nanobubble evolution and measurable performance improvement at high current densities. This finding opens a route to mitigate bubble-induced activity loss in OER electrodes.
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