Electrochemical quartz crystal microbalance and in situ infrared spectroscopic studies on the redox reaction of Prussian blue

被引:43
作者
Ogura, K [1 ]
Nakayama, M [1 ]
Nakaoka, K [1 ]
机构
[1] Yamaguchi Univ, Dept Appl Chem, Ube, Yamaguchi 7558611, Japan
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1999年 / 474卷 / 02期
关键词
EQCM; in situ FTIR; Prussian blue;
D O I
10.1016/S0022-0728(99)00306-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The redox reaction of freshly prepared and well cycled Prussian blue (PB) films has been studied by means of an electrochemical quartz crystal microbalance (EQCM) and in situ Fourier transform infrared (FTIR) reflection spectroscopy. In the first reduction, insoluble PB (Fe-4(3+)[Fe-11(CN)(6)](3). 6H(2)O) was found to be converted irreversibly to Everitt's salt (ES, K2Fe2+[Fe-11(CN)(6)]) by incorporating 6 mol of potassium ions, and 6 mol of water molecules coordinated to iron ions are released simultaneously. The change in molar mass estimated from this reaction was the gain of 17.7 g mol(-1) per mol electrons, which was close to the observed value. The reoxidation of ES results in the formation of soluble PB (KFe3+[Fe-11(CN)(6)]) and the concurrent release of potassium ions, and water molecules are introduced to interstitial positions in the PB lattice. The reversible change between soluble PB and ES takes place in further repeated potential cycling. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:101 / 106
页数:6
相关论文
共 15 条
[1]   CRYSTAL-STRUCTURE OF PRUSSIAN BLUE - FE4[FE(CN)6]3.XH2O [J].
BUSER, HJ ;
SCHWARZENBACH, D ;
PETTER, W ;
LUDI, A .
INORGANIC CHEMISTRY, 1977, 16 (11) :2704-2710
[2]   A STUDY OF ELECTROCHEMICALLY GROWN PRUSSIAN BLUE FILMS USING FOURIER-TRANSFORM INFRARED-SPECTROSCOPY [J].
CHRISTENSEN, PA ;
HAMNETT, A ;
HIGGINS, SJ .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1990, (07) :2233-2238
[3]  
Davidson D., 1937, J CHEM EDUC, V14, P277, DOI DOI 10.1021/ED014P277
[4]   ELECTROCHROMISM IN THE MIXED-VALENCE HEXACYANIDES .1. VOLTAMMETRIC AND SPECTRAL STUDIES OF THE OXIDATION AND REDUCTION OF THIN-FILMS OF PRUSSIAN BLUE [J].
ELLIS, D ;
ECKHOFF, M ;
NEFF, VD .
JOURNAL OF PHYSICAL CHEMISTRY, 1981, 85 (09) :1225-1231
[5]   ION FLUX DURING ELECTROCHEMICAL CHARGING OF PRUSSIAN BLUE FILMS [J].
FELDMAN, BJ ;
MELROY, OR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 234 (1-2) :213-227
[6]   NEUTRON-DIFFRACTION STUDY OF PRUSSIAN BLUE, FE4[FE(CN)6]3.XH2O - LOCATION OF WATER-MOLECULES AND LONG-RANGE MAGNETIC ORDER [J].
HERREN, F ;
FISCHER, P ;
LUDI, A ;
HALG, W .
INORGANIC CHEMISTRY, 1980, 19 (04) :956-959
[7]   SPECTROELECTROCHEMISTRY AND ELECTROCHEMICAL PREPARATION METHOD OF PRUSSIAN BLUE MODIFIED ELECTRODES [J].
ITAYA, K ;
ATAKA, T ;
TOSHIMA, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (18) :4767-4772
[8]   ELECTROCHEMISTRY OF POLYNUCLEAR TRANSITION-METAL CYANIDES - PRUSSIAN BLUE AND ITS ANALOGS [J].
ITAYA, K ;
UCHIDA, I ;
NEFF, VD .
ACCOUNTS OF CHEMICAL RESEARCH, 1986, 19 (06) :162-168
[9]   MASS MEASUREMENTS USING ISOTOPICALLY LABELED SOLVENTS REVEAL THE EXTENT OF SOLVENT TRANSPORT DURING REDOX IN THIN-FILMS ON ELECTRODES [J].
LASKY, SJ ;
BUTTRY, DA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (18) :6258-6260
[10]   IRON HEXACYANOFERRATE FILMS - SPECTROELECTROCHEMICAL DISTINCTION AND ELECTRODEPOSITION SEQUENCE OF SOLUBLE (K+-CONTAINING) AND INSOLUBLE (K+-FREE) PRUSSIAN BLUE, AND COMPOSITION CHANGES IN POLYELECTROCHROMIC SWITCHING [J].
MORTIMER, RJ ;
ROSSEINSKY, DR .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1984, (09) :2059-2061