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The passivation mechanism of Fe in the acidic AlCl_3-EMIC ionic liquid 被引量:2

The passivation mechanism of Fe in the acidic AlCl_3-EMIC ionic liquid
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摘要 The passivation behavior of Fe in the acidic AlCl_3-1-ethyl-3-methyl-imidazolium chloride(AlCl_3-EMIC) ionic liquid was studied by linear sweep voltammetry and chonopotentiometry. Various approaches were used to characterize the composition and morphology of passive film formed on the Fe electrode, such as scanning electron microscopy(SEM), Raman spectra and X-ray Photoelectron Spectroscopy(XPS). The results showed that the critical passivation potential of Fe shifted to more negative when the molar ratio of AlCl_3:EMIC changing from 2 to 1.3.A film with a light yellow color was observed on the surface of the Fe electrode after passivation. The composition of the passive film was demonstrated to be FeCl_2. The passive film was composed of particulate FeCl_2 with average diameter of about 500 nm. The formation of FeCl_2 film was attributed to the variation of the electrolyte Lewis acidity from acidic to neutral at the interface during the dissolution process of Fe. The reason caused the variation of the electrolyte acidity was discussed. The passivation behavior of Fe in the acidic AlCl_3-1-ethyl-3-methyl-imidazolium chloride(AlCl_3-EMIC) ionic liquid was studied by linear sweep voltammetry and chonopotentiometry. Various approaches were used to characterize the composition and morphology of passive film formed on the Fe electrode, such as scanning electron microscopy(SEM), Raman spectra and X-ray Photoelectron Spectroscopy(XPS). The results showed that the critical passivation potential of Fe shifted to more negative when the molar ratio of AlCl_3:EMIC changing from 2 to 1.3.A film with a light yellow color was observed on the surface of the Fe electrode after passivation. The composition of the passive film was demonstrated to be FeCl_2. The passive film was composed of particulate FeCl_2 with average diameter of about 500 nm. The formation of FeCl_2 film was attributed to the variation of the electrolyte Lewis acidity from acidic to neutral at the interface during the dissolution process of Fe. The reason caused the variation of the electrolyte acidity was discussed.
出处 《Green Energy & Environment》 SCIE 2017年第4期412-418,共7页 绿色能源与环境(英文版)
基金 the National Natural Science Foundation of China(No.51271166)
关键词 Passivation mechanism FE Ionic liquid Passive film FeCl2 Passivation mechanism Fe Ionic liquid Passive film FeCl2
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