化学反应
化学物理
氧化还原
化学种类
化学动力学
化学
化学动力学
化学过程
电化学
材料科学
化学状态
动力学
分析化学(期刊)
限制
接口(物质)
反应动力学
电荷(物理)
反应速率
电介质
接触带电
时间分辨率
化学稳定性
集聚经济
反应机理
纳米技术
无机化学
化学工程
电极
催化作用
化学反应器
传质
带电粒子
稳态(化学)
弹道
瞬态(计算机编程)
作者
Jinyang Zhang,Xuejiao Wang,Ning Wu,Guangxiang Gu,Zhong Lin Wang
摘要
Real-time monitoring of microscopic chemical reactions offers valuable insight into reaction mechanisms, intermediate species, and the reaction kinetics involved. Mainstream electrochemical and chromatographic techniques are often complex, low-sensitivity, failing to capture transient phenomena or distinguish similar chemical species within the reaction, limiting their accessibility for real-time and continuing monitoring. Here, high-resolution interface charge transfer mapping (ICTM) generated by liquid-solid contact electrification is used in situ for continuously monitoring potential chemical changes in the reactions. As liquid reactants slide dropwise over time along an insulating reclined plane, the ICTMs along the sample trajectory over time are recorded and is used to analysis chemical changes within the reactions. By means of time-resolved ICTM measurements at statically charged dielectric surface, we have probed the dynamic evolution of redox reactions, tracked the organocatalytic reactions, and evaluated the agglomeration state of metal catalysts with a time resolution on the scale of seconds.
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