X射线光电子能谱
钝化
溶解
材料科学
腐蚀
合金
高熵合金
俄歇电子能谱
氧化物
二次离子质谱法
分析化学(期刊)
硫酸
过渡金属
表层
化学工程
冶金
离子
图层(电子)
化学
纳米技术
物理化学
生物化学
物理
有机化学
色谱法
核物理学
工程类
催化作用
作者
Pei-Chen Huang,Po-Chih Chu,Ting-Jia Yang,Ji-Zhen Wang,Wei‐Chun Lin
标识
DOI:10.1016/j.apsusc.2023.158942
摘要
Recently, high-entropy alloys (HEAs) have demonstrated excellent properties, such as high yield strength, better ductility, and great corrosion resistance, which breaks the conventional alloy design strategy. We investigate the corrosion behavior of AlCoCrFeNi HEAs in 0.5 M H2SO4 solution under ambient conditions using soft and hard X-ray photoelectron spectroscopy (XPS) for surface/bulk (∼5 nm and > 10 nm) analysis. The composition information of the surface and bulk can be achieved and compared via a switchable target system, where the Al (Kα, 1486.6 eV) and Cr (Kα, 5414.8 eV) targets produced X-rays for regular XPS and hard X-ray photoelectron spectroscopy (HAXPES) as the detection source, respectively. The HAXPES provides a precise composition study in the bulk region without the interference of Auger electron signals caused by neighboring transition metals. The dissolution of metallic ions in H2SO4 solution were collected by inductively coupled plasma–mass spectrometry (ICP–MS) and compared with the XPS-HAXPES analysis. The Al and Cr compounds redeposited to the HEA surface, while Fe, Co, and Ni kept dissolving into the acidic solution. It is speculated that the dissolution of Fe, Ni, and especially Co could slow the rate of dissolution of Cr. The passivation layer formed by Cr hydroxide/oxide could thus protect the HEA from further corrosion. Al easily leached before the formation of the Cr passivation layer, however, Al compounds still became the main species on the surface of the HEA. Moreover, our findings examined by the novel analysis technique may provide a new paradigm for the quantification study of HEAs.
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