激进的
超氧化物
碰撞
化学
计算机科学
生物化学
计算机安全
酶
作者
Jin Xu,Chengzhuo Yu,Fengjie Chen,Feifei Li,Wanchao Yu,Silong Wang,Xiong Li,Fanglan Geng,Jitao Lv,Xianwei Wang,Lixia Zhao,Yawei Wang,Guibin Jiang
标识
DOI:10.1002/anie.202511594
摘要
Spontaneous generation of reactive oxygen species (ROS) driven by water-solid contact electrification was a new source of redox chemistry. However, superoxide radicals (O2 •-), a kind of ROS that was of great significance in both natural and engineering environments, remain overlooked and poorly understood at the water-solid interface. Here, we found O2 •- could be generated spontaneously when water collided with the solid interface even under dark conditions, and its production was quantified by CL. 18O isotope labelling experiments and solid-liquid contact electrification detection confirmed that the generation of O2 •- was from the reduction of dissolved oxygen by electrons at the water-solid interface and that the kinetic energy of the water energized the reaction. Given the ubiquitous nature of solid-liquid collisions, such as rain colliding with mineral surfaces during rainfall, we further systematically investigated the O2 •- generation and their decay kinetics at three distinct rain-mineral interfaces. Results showed that O2 •- generation ranged from 0.015 to 1.1 nM, comparable to the O2 •- production by photochemical pathways. Our findings established the water-solid collision interface as a previously unrecognized global source of O2 •- and highlight a universal yet overlooked physicochemical mechanism underpinning multiphase redox chemistry.
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