Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Wenhua Road 72, 110016, Shenyang, China.
Electrochemistry and Materials Science Research Laboratory, Department of Chemistry, Federal University of Technology Owerri, PMB, Owerri, 1526, Nigeria.
Nat Commun. 2018 Jul 2;9(1):2559. doi: 10.1038/s41467-018-04942-x.
Nanometer-thick passive films on metals usually impart remarkable resistance to general corrosion but are susceptible to localized attack in certain aggressive media, leading to material failure with pronounced adverse economic and safety consequences. Over the past decades, several classic theories have been proposed and accepted, based on hypotheses and theoretical models, and oftentimes, not sufficiently nor directly corroborated by experimental evidence. Here we show experimental results on the structure of the passive film formed on a FeCrNi single crystal in chloride-free and chloride-containing media. We use aberration-corrected transmission electron microscopy to directly capture the chloride ion accumulation at the metal/film interface, lattice expansion on the metal side, undulations at the interface, and structural inhomogeneity on the film side, most of which had previously been rejected by existing models. This work unmasks, at the atomic scale, the mechanism of chloride-induced passivity breakdown that is known to occur in various metallic materials.
金属表面的纳米级无源膜通常具有显著的抗一般腐蚀性,但在某些腐蚀性介质中容易受到局部侵蚀,从而导致材料失效,带来严重的经济和安全后果。在过去的几十年中,已经提出并接受了几种经典理论,这些理论基于假设和理论模型,并且在很多情况下,没有得到实验证据的充分或直接证实。在这里,我们展示了在无氯和含氯介质中形成的 FeCrNi 单晶体上的无源膜结构的实验结果。我们使用相衬校正透射电子显微镜直接捕获金属/膜界面处的氯离子积累、金属侧的晶格膨胀、界面上的波动以及膜侧的结构不均匀性,其中大部分以前被现有模型所拒绝。这项工作在原子尺度上揭示了已知在各种金属材料中发生的氯化物诱导钝化失效的机制。