Voltage-induced infrared absorption from a spin-cast thin film of ferroelectric poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE))

Kenji Takashima, Yukio Furukawa

    研究成果: Article

    1 引用 (Scopus)

    抄録

    Voltage-induced infrared spectra of annealed spin-cast thin films of ferroelectric poly(vinylidene fluoride-cotrifluoroethylene) (P(VDF-TrFE)) (molar ratio, 3:1) were measured in a stepwise cyclic external electric field. Most of the observed infrared bands originated from the β ferroelectric crystalline phase. The voltage-induced spectral changes were decomposed into zeroth- (original), first-, and second-derivative spectra, and were attributed to the rotational motions of the polymer chains and the vibrational Stark effect. The values of the original spectral absorbance change ratios, ΔA/A, for the 849-cm-1 band (CF2 symmetric stretching, a1) and the 884-cm-1 band (CH2 rocking, b2) of the film exhibited double minimum and maximum peak hysteresis loops, respectively. The intensity of each band increased or decreased suddenly near a coercive field of ±0.6 MV/cm. These sudden intensity changes were attributed to the rotational inversion of the polymer chains that are associated with ferroelectricity.

    元の言語English
    ページ(範囲)59-64
    ページ数6
    ジャーナルAnalytical Sciences
    33
    発行部数1
    出版物ステータスPublished - 2017

    Fingerprint

    Infrared absorption
    Ferroelectric materials
    Polymers
    Infrared radiation
    Stark effect
    Ferroelectricity
    Thin films
    Electric potential
    Hysteresis loops
    Stretching
    Electric fields
    Crystalline materials
    Derivatives
    polyvinylidene fluoride
    trifluoroethene

    ASJC Scopus subject areas

    • Analytical Chemistry

    これを引用

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    abstract = "Voltage-induced infrared spectra of annealed spin-cast thin films of ferroelectric poly(vinylidene fluoride-cotrifluoroethylene) (P(VDF-TrFE)) (molar ratio, 3:1) were measured in a stepwise cyclic external electric field. Most of the observed infrared bands originated from the β ferroelectric crystalline phase. The voltage-induced spectral changes were decomposed into zeroth- (original), first-, and second-derivative spectra, and were attributed to the rotational motions of the polymer chains and the vibrational Stark effect. The values of the original spectral absorbance change ratios, ΔA/A, for the 849-cm-1 band (CF2 symmetric stretching, a1) and the 884-cm-1 band (CH2 rocking, b2) of the film exhibited double minimum and maximum peak hysteresis loops, respectively. The intensity of each band increased or decreased suddenly near a coercive field of ±0.6 MV/cm. These sudden intensity changes were attributed to the rotational inversion of the polymer chains that are associated with ferroelectricity.",
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    AU - Furukawa, Yukio

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    N2 - Voltage-induced infrared spectra of annealed spin-cast thin films of ferroelectric poly(vinylidene fluoride-cotrifluoroethylene) (P(VDF-TrFE)) (molar ratio, 3:1) were measured in a stepwise cyclic external electric field. Most of the observed infrared bands originated from the β ferroelectric crystalline phase. The voltage-induced spectral changes were decomposed into zeroth- (original), first-, and second-derivative spectra, and were attributed to the rotational motions of the polymer chains and the vibrational Stark effect. The values of the original spectral absorbance change ratios, ΔA/A, for the 849-cm-1 band (CF2 symmetric stretching, a1) and the 884-cm-1 band (CH2 rocking, b2) of the film exhibited double minimum and maximum peak hysteresis loops, respectively. The intensity of each band increased or decreased suddenly near a coercive field of ±0.6 MV/cm. These sudden intensity changes were attributed to the rotational inversion of the polymer chains that are associated with ferroelectricity.

    AB - Voltage-induced infrared spectra of annealed spin-cast thin films of ferroelectric poly(vinylidene fluoride-cotrifluoroethylene) (P(VDF-TrFE)) (molar ratio, 3:1) were measured in a stepwise cyclic external electric field. Most of the observed infrared bands originated from the β ferroelectric crystalline phase. The voltage-induced spectral changes were decomposed into zeroth- (original), first-, and second-derivative spectra, and were attributed to the rotational motions of the polymer chains and the vibrational Stark effect. The values of the original spectral absorbance change ratios, ΔA/A, for the 849-cm-1 band (CF2 symmetric stretching, a1) and the 884-cm-1 band (CH2 rocking, b2) of the film exhibited double minimum and maximum peak hysteresis loops, respectively. The intensity of each band increased or decreased suddenly near a coercive field of ±0.6 MV/cm. These sudden intensity changes were attributed to the rotational inversion of the polymer chains that are associated with ferroelectricity.

    KW - Ferroelectricity

    KW - Infrared spectroscopy

    KW - Poly(vinylidene fluoride-co-trifluoroethylene)

    KW - Thin film

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