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    KCI등재 SCI SCIE SCOPUS

    Photoelectrochemical Analysis of the Effects of pH and Sulfate Ions on the Structure and the Composition of the Passive Film Formed on Fe-20Cr-15Ni Alloy

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    https://www.riss.kr/link?id=A104267652

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr-
    15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra
    for the passive film formed on Fe-20Cr-15Ni in the buffer solutions are composed of two spectral components,
    one of which is generated from Cr-substituted γ-Fe2O3 and the other of which is generated from NiO. However,
    the passive film formed in sulfate solutions showed only the photocurrent spectrum of Cr-substituted γ-Fe2O3,
    suggesting that the formation of NiO in the passive film is suppressed because of a severe selective dissolution
    of Ni in the presence of sulfate ions. Mott-Schottky plots confirmed that the base structure of the passive film
    on Fe-20Cr-15Ni is n-type (Cr, Ni)-substituted γ-Fe2O3 regardless of solution pH and sulfate ions. The photocurrent
    intensity, flat band potential, and donor density for the passive film varied depending on the solution
    pH or the presence of sulfate ions in the solution, due primarily to the Cr enrichment in the film caused by the
    preferential dissolution of Fe and Ni that is more appreciable in highly acidic solutions containing sulfate ions.
    번역하기

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr- 15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra for the passive film formed on F...

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr-
    15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra
    for the passive film formed on Fe-20Cr-15Ni in the buffer solutions are composed of two spectral components,
    one of which is generated from Cr-substituted γ-Fe2O3 and the other of which is generated from NiO. However,
    the passive film formed in sulfate solutions showed only the photocurrent spectrum of Cr-substituted γ-Fe2O3,
    suggesting that the formation of NiO in the passive film is suppressed because of a severe selective dissolution
    of Ni in the presence of sulfate ions. Mott-Schottky plots confirmed that the base structure of the passive film
    on Fe-20Cr-15Ni is n-type (Cr, Ni)-substituted γ-Fe2O3 regardless of solution pH and sulfate ions. The photocurrent
    intensity, flat band potential, and donor density for the passive film varied depending on the solution
    pH or the presence of sulfate ions in the solution, due primarily to the Cr enrichment in the film caused by the
    preferential dissolution of Fe and Ni that is more appreciable in highly acidic solutions containing sulfate ions.

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr-
    15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra
    for the passive film formed on Fe-20Cr-15Ni in the buffer solutions are composed of two spectral components,
    one of which is generated from Cr-substituted γ-Fe2O3 and the other of which is generated from NiO. However,
    the passive film formed in sulfate solutions showed only the photocurrent spectrum of Cr-substituted γ-Fe2O3,
    suggesting that the formation of NiO in the passive film is suppressed because of a severe selective dissolution
    of Ni in the presence of sulfate ions. Mott-Schottky plots confirmed that the base structure of the passive film
    on Fe-20Cr-15Ni is n-type (Cr, Ni)-substituted γ-Fe2O3 regardless of solution pH and sulfate ions. The photocurrent
    intensity, flat band potential, and donor density for the passive film varied depending on the solution
    pH or the presence of sulfate ions in the solution, due primarily to the Cr enrichment in the film caused by the
    preferential dissolution of Fe and Ni that is more appreciable in highly acidic solutions containing sulfate ions.
    번역하기

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr- 15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra for the passive film formed on...

    The effects of pH and sulfate ions on the structure and compositions of the passive film formed on Fe-20Cr-
    15Ni were examined using a photoelectrochemical technique and Mott-Schottky analysis. The photocurrent spectra
    for the passive film formed on Fe-20Cr-15Ni in the buffer solutions are composed of two spectral components,
    one of which is generated from Cr-substituted γ-Fe2O3 and the other of which is generated from NiO. However,
    the passive film formed in sulfate solutions showed only the photocurrent spectrum of Cr-substituted γ-Fe2O3,
    suggesting that the formation of NiO in the passive film is suppressed because of a severe selective dissolution
    of Ni in the presence of sulfate ions. Mott-Schottky plots confirmed that the base structure of the passive film
    on Fe-20Cr-15Ni is n-type (Cr, Ni)-substituted γ-Fe2O3 regardless of solution pH and sulfate ions. The photocurrent
    intensity, flat band potential, and donor density for the passive film varied depending on the solution
    pH or the presence of sulfate ions in the solution, due primarily to the Cr enrichment in the film caused by the
    preferential dissolution of Fe and Ni that is more appreciable in highly acidic solutions containing sulfate ions.

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    참고문헌 (Reference)

    1 C. Sunseri, 134 : 2410-, 1987

    2 A. Di Paola, 26 : 935-, 1986

    3 D. D. Macdonald, 139 : 170-, 1992

    4 A. M. P. Simoes, 137 : 82-, 1990

    5 E. A. Cho, 47 : 1661-, 2002

    6 E. A. Cho, 50 : 3383-, 2005

    7 N. E. Hakiki, 37 : 1809-, 1998

    8 H. Tsuchiya, 47 : 4357-, 2002

    9 V. Maurice, 145 : 909-, 1998

    10 M. Bojinov, 107 : 5101-, 2003

    1 C. Sunseri, 134 : 2410-, 1987

    2 A. Di Paola, 26 : 935-, 1986

    3 D. D. Macdonald, 139 : 170-, 1992

    4 A. M. P. Simoes, 137 : 82-, 1990

    5 E. A. Cho, 47 : 1661-, 2002

    6 E. A. Cho, 50 : 3383-, 2005

    7 N. E. Hakiki, 37 : 1809-, 1998

    8 H. Tsuchiya, 47 : 4357-, 2002

    9 V. Maurice, 145 : 909-, 1998

    10 M. Bojinov, 107 : 5101-, 2003

    11 J. S. Kim, 43 : 1403-, 2001

    12 H. J. Jang, 50 : 3503-, 2005

    13 M. Bojinov, 41 : 1557-, 1999

    14 D. Y. Kim, 513 : 212-, 2006

    15 H. J. Jang, 590 : 120-, 2006

    16 S. J. Ahn, 49 : 3347-, 2004

    17 J. S. Kim, 47 : 415-, 2002

    18 S. J. Lee, 46 : 2605-, 2001

    19 U. Stimming, 31 : 415-, 1986

    20 A. Michaelis, 106 : 483-, 1996

    21 G. Lorang, 141 : 3347-, 1994

    22 M. Da Cunha Belo, 44 : 2473-, 1999

    23 C. M. Abreu, 51 : 2991-, 2006

    24 N. Hara, 31 : 154-, 1991

    25 N. E. Hakiki, 145 : 3821-, 1998

    26 A. Di Paola, 34 : 203-, 1989

    27 N. E. Hakiki, 143 : 3088-, 1996

    28 B. MacDougall, "Corrosion Mechanisms in Theory and Practice" Marcel Dekker, Inc. 1995

    29 Yu. V. Pleskov, "Comprehensive Treatise of Electrochemistry" Ch .6, Plenum Press 1980

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