Spectroscopic and electrochemical characterizations of dilithium octacyanophthalocyanine Langmuir-Blodgett films

Hong Qi Xiangk, Keiji Tanaka, Atsushi Takahara, Tisato Kajiyama

研究成果: ジャーナルへの寄稿記事

23 引用 (Scopus)

抄録

Langmuir-Blodgett (LB) films of dilithium octacyanophthalocyanine [Li2Pc(CN)8] were first prepared, and their electrochemical reduction/reoxidation behaviors were studied in detail. An overwhelming majority of the Li2Pc(CN)8 molecules in the LB film were stacked in a face-to-face aggregated state and stood obliquely with an edge-on configuration on the substrate surface. Two overlapping redox waves were observed in the voltammogram of the LB film in 1 mol dm-3 HCl solution. Their relative intensity was found to be largely dependent on the molecular aggregation state in the film. On the basis of spectroscopic and electrochemical analyses, the first and second reduction waves upon cathodic potential scanning were principally assigned to the aggregated and monomeric Li2Pc(CN)8 molecules, respectively, in the solid film structure. In comparison with the corresponding solvent-cast film, charge transfer within the LB film and/or through the electrode interface was facilitated, and the LB film showed excellent dynamic character in the redox process.

元の言語英語
ページ(範囲)2223-2228
ページ数6
ジャーナルLangmuir
18
発行部数6
DOI
出版物ステータス出版済み - 3 19 2002

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Langmuir Blodgett films
Langmuir-Blodgett films
Molecules
Charge transfer
casts
molecules
Agglomeration
charge transfer
Scanning
Electrodes
scanning
electrodes
Substrates
configurations
Oxidation-Reduction

All Science Journal Classification (ASJC) codes

  • Materials Science(all)
  • Condensed Matter Physics
  • Surfaces and Interfaces
  • Spectroscopy
  • Electrochemistry

これを引用

Spectroscopic and electrochemical characterizations of dilithium octacyanophthalocyanine Langmuir-Blodgett films. / Xiangk, Hong Qi; Tanaka, Keiji; Takahara, Atsushi; Kajiyama, Tisato.

:: Langmuir, 巻 18, 番号 6, 19.03.2002, p. 2223-2228.

研究成果: ジャーナルへの寄稿記事

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abstract = "Langmuir-Blodgett (LB) films of dilithium octacyanophthalocyanine [Li2Pc(CN)8] were first prepared, and their electrochemical reduction/reoxidation behaviors were studied in detail. An overwhelming majority of the Li2Pc(CN)8 molecules in the LB film were stacked in a face-to-face aggregated state and stood obliquely with an edge-on configuration on the substrate surface. Two overlapping redox waves were observed in the voltammogram of the LB film in 1 mol dm-3 HCl solution. Their relative intensity was found to be largely dependent on the molecular aggregation state in the film. On the basis of spectroscopic and electrochemical analyses, the first and second reduction waves upon cathodic potential scanning were principally assigned to the aggregated and monomeric Li2Pc(CN)8 molecules, respectively, in the solid film structure. In comparison with the corresponding solvent-cast film, charge transfer within the LB film and/or through the electrode interface was facilitated, and the LB film showed excellent dynamic character in the redox process.",
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AU - Xiangk, Hong Qi

AU - Tanaka, Keiji

AU - Takahara, Atsushi

AU - Kajiyama, Tisato

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N2 - Langmuir-Blodgett (LB) films of dilithium octacyanophthalocyanine [Li2Pc(CN)8] were first prepared, and their electrochemical reduction/reoxidation behaviors were studied in detail. An overwhelming majority of the Li2Pc(CN)8 molecules in the LB film were stacked in a face-to-face aggregated state and stood obliquely with an edge-on configuration on the substrate surface. Two overlapping redox waves were observed in the voltammogram of the LB film in 1 mol dm-3 HCl solution. Their relative intensity was found to be largely dependent on the molecular aggregation state in the film. On the basis of spectroscopic and electrochemical analyses, the first and second reduction waves upon cathodic potential scanning were principally assigned to the aggregated and monomeric Li2Pc(CN)8 molecules, respectively, in the solid film structure. In comparison with the corresponding solvent-cast film, charge transfer within the LB film and/or through the electrode interface was facilitated, and the LB film showed excellent dynamic character in the redox process.

AB - Langmuir-Blodgett (LB) films of dilithium octacyanophthalocyanine [Li2Pc(CN)8] were first prepared, and their electrochemical reduction/reoxidation behaviors were studied in detail. An overwhelming majority of the Li2Pc(CN)8 molecules in the LB film were stacked in a face-to-face aggregated state and stood obliquely with an edge-on configuration on the substrate surface. Two overlapping redox waves were observed in the voltammogram of the LB film in 1 mol dm-3 HCl solution. Their relative intensity was found to be largely dependent on the molecular aggregation state in the film. On the basis of spectroscopic and electrochemical analyses, the first and second reduction waves upon cathodic potential scanning were principally assigned to the aggregated and monomeric Li2Pc(CN)8 molecules, respectively, in the solid film structure. In comparison with the corresponding solvent-cast film, charge transfer within the LB film and/or through the electrode interface was facilitated, and the LB film showed excellent dynamic character in the redox process.

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