In Situ Electrochemical Atomic Force Microscopy and Auger Electro Spectroscopy Study on the Passive Film Structure of 2024-T3 Aluminum Alloy Combined with a Density Functional Theory Calculation

被引:32
作者
Li, Ni [1 ]
Dong, Chaofang [1 ]
Man, Chen [1 ]
Yao, Jizheng [1 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Key Lab Corros & Protect MOE, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Auger electro spectroscopy; density functional theory calculations; electrochemical atomic force microscopy; passive films; ANODIC OXIDE FORMATION; STAINLESS-STEEL; OXIDATION; CORROSION; BEHAVIOR; DFT; MICROSTRUCTURE; ADSORPTION;
D O I
10.1002/adem.201900386
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The initial growth of the passive films on the Al2CuMg particle and Al matrix in AA2024-T3 are investigated by in situ electrochemical atomic force microscopy (ECAFM) and ex situ characterization techniques in citric acid. The passive films are mainly composed of Al2O3 (34%), Al(OH)(3) (8.4%), AlOOH (27.2%), CuO (19.4%), and Cu2O (11%). ECAFM images display that the film on the Al2CuMg particle is flawed and loose. Auger electro spectroscopy (AES) results show that the thickness of the passive film on the Al2CuMg particle is 1.4 nm, which is thinner than that on the Al matrix (2.4 nm). The combined ECAFM and AES results demonstrate that the corrosion resistance of the passive film on the Al2CuMg is weaker than that on the Al matrix. According to the density functional theory (DFT) calculations, the average charge transfer and adsorption energy of the adsorbates (O2-/OH-/H2O) on the Al surfaces are larger than that on the Al2CuMg surfaces, meaning that O-2 and H2O preferably dissociate and adsorb on the Al surfaces. Moreover, the electronic interactions between the adsorbates and Al surfaces are stronger. This is the reason that the growth rate of the passive film on the Al2CuMg particle is slower at initial stages.
引用
收藏
页数:11
相关论文
共 37 条
  • [1] Electrochemical behaviour of a copper-aluminium alloy in concentrated alkaline solutions
    Ashour, EA
    Ateya, BG
    [J]. ELECTROCHIMICA ACTA, 1997, 42 (02) : 243 - 250
  • [2] Dissociation of O2 at Al(111):: The role of spin selection rules -: art. no. 036104
    Behler, J
    Delley, B
    Lorenz, S
    Reuter, K
    Scheffler, M
    [J]. PHYSICAL REVIEW LETTERS, 2005, 94 (03)
  • [3] In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy
    Bertram, F.
    Zhang, F.
    Evertsson, J.
    Carla, F.
    Pan, J.
    Messing, M. E.
    Mikkelsen, A.
    Nilsson, J-O
    Lundgren, E.
    [J]. JOURNAL OF APPLIED PHYSICS, 2014, 116 (03)
  • [4] A closer look at constituent induced localised corrosion in Al-Cu-Mg alloys
    Birbilis, N.
    Zhu, Y. M.
    Kairy, S. K.
    Glenn, M. A.
    Nie, J. -F.
    Morton, A. J.
    Gonzalez-Garcia, Y.
    Terryn, H.
    Mol, J. M. C.
    Hughes, A. E.
    [J]. CORROSION SCIENCE, 2016, 113 : 160 - 171
  • [5] Susceptibility to pitting corrosion of 6056 aluminium alloy
    Blanc, C
    Mankowski, G
    [J]. CORROSION SCIENCE, 1997, 39 (05) : 949 - 959
  • [6] Tuning the Limiting Thickness of a Thin Oxide Layer on Al(111) with Oxygen Gas Pressure
    Cai, Na
    Zhou, Guangwen
    Mueller, Kathrin
    Starr, David E.
    [J]. PHYSICAL REVIEW LETTERS, 2011, 107 (03)
  • [7] Intercalation of pyrazine in layered copper nitroprusside: Synthesis, crystal structure and XPS study
    Cano, A.
    Rodriguez-Hernandez, J.
    Shchukarev, A.
    Reguera, E.
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 2019, 273 : 1 - 10
  • [8] Cote J., 1969, Plating, V56, P386
  • [9] Residual flaws due to formation of oxygen bubbles in anodic alumina
    Crossland, AC
    Habazaki, H
    Shimizu, K
    Skeldon, P
    Thompson, GE
    Wood, GC
    Zhou, X
    Smith, CJE
    [J]. CORROSION SCIENCE, 1999, 41 (10) : 1945 - 1954
  • [10] Preferential anodic oxidation of second-phase constituents during anodising of AA2024-T3 and AA7075-T6 alloys
    de Miera, M. Saenz
    Curioni, M.
    Skeldon, P.
    Thompson, G. E.
    [J]. SURFACE AND INTERFACE ANALYSIS, 2010, 42 (04) : 241 - 246