催化作用
激进的
反应性(心理学)
羟基自由基
化学工程
化学
声化学
氢氧化物
污染物
离子
光化学
纳米尺度
材料科学
纳米技术
化学过程
氮气
化学反应
化学发光
纳米颗粒
降级(电信)
硝酸盐
环境修复
原位
活性氮物种
过程(计算)
环境化学
析氧
作者
Siyu Yang,Wei Wang,Jie‐Jie Chen,Joseph S. Francisco,Xian‐Wei Liu
标识
DOI:10.1038/s41467-025-63899-w
摘要
Gas–liquid interfaces at the micro- and nanoscale are emerging hotspots for unique chemical reactivity, yet the reactivity of individual microbubbles remains largely unexplored. Here, we visualize the catalyst-free generation of reactive oxygen species, particularly hydroxyl radicals, at the gas‒liquid interface of microbubbles. In-situ chemiluminescence imaging, together with spectroscopic analyses, and multiscale computational simulations shows that the enrichment of hydroxide ions at the microbubble surface, coupled with the interfacial electric field, drives the catalyst-free generation of hydroxyl radicals. The generated hydroxyl radicals enable efficient degradation of organic pollutants and facilitate the conversion of nitrogen into nitrate ions under mild conditions, highlighting the practical applicability of this catalyst-free process in environmental remediation and sustainable nitrogen fixation. These findings provide new insights into catalyst-free radical chemistry at gas–liquid interfaces, with significant implications for catalytic processes, sustainable chemical manufacturing, and environmental catalysis. Microbubble interfaces exhibit unique chemical reactivity. Here, the authors visualize catalyst-free hydroxyl radical generation at nitrogen microbubbles, enabling pollutant degradation and sustainable nitrogen fixation under mild conditions.
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