化学
氧化物
氧化铁
成核
相(物质)
焊剂(冶金)
金属
腐蚀
催化作用
动力学
化学物理
化学工程
外延
过渡金属
化学稳定性
化学反应
纳米技术
氧化还原
氧气
图层(电子)
氧化法
催化氧化
赤铁矿
磁铁矿
硫化铁
钨铁矿
多相催化
无机化学
冶金
反应中间体
不稳定性
作者
Wei Tu,Shuoqi Zhang,Zhen Zeng,Shaobo Han,Yixuan Wen,T. D. Xu,Fan Zhang,Xiaoben Zhang,Hui Li,Xia Song,Y ZHAO,Hui Li,Yongfu Tang,Lianfeng Zou,Xiaobo Chen,Xianhu Sun,Yi Gao,Yao Yang,Wei Liu,F CHEN
摘要
Iron oxidation is a fundamental chemical transformation underpinning planetary evolution and technologies ranging from steel metallurgy and corrosion to catalysis and magnetic storage. Despite decades of surface-science research elucidating oxidation kinetics and surface dynamics, the atomic-scale transformations occurring beneath the surface during the incipient stages of oxidation have remained largely inaccessible. Here we directly visualize the atomic genesis of iron oxidation using in situ environmental scanning/transmission electron microscopy (ETEM/ESTEM). We reveal that oxidation begins with the nucleation of an epitaxial FeO layer on metallic iron. Once the FeO film reaches a critical thickness, a lattice-template–driven phase transformation is triggered at the buried FeO/Fe interface, rather than at the gas-exposed surface, leading to the formation of the higher-valence oxide phase Fe 3 O 4 . This interfacial transformation drives a concerted outward flux of iron cations, continuously regenerating a ∼two-monolayer FeO skin atop a thickening Fe 3 O 4 underlayer. This process results in a persistent, self-regulating FeO/Fe 3 O 4 /Fe trilayer architecture that directly contradicts the prevailing assumption that oxidation states monotonically increase toward the gas–solid interface. By identifying this counterintuitive, interface-driven mechanism, our results provide the missing atomic-scale link for understanding oxide stability and phase evolution in reactive environments.
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