CHARGE-TRANSFER DISTANCE BETWEEN TRIS(2,2'-BIPYRIDINE)RUTHENIUM(II) REDOX CENTERS INCORPORATED IN NAFION(R) MEMBRANE

被引:44
作者
YAGI, M
NAGAI, K
KIRA, A
KANEKO, M
机构
[1] IBARAKI UNIV,DEPT CHEM,MITO,IBARAKI 310,JAPAN
[2] RIKEN,INST PHYS & CHEM RES,WAKO,SAITAMA 35101,JAPAN
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1995年 / 394卷 / 1-2期
关键词
CHARGE TRANSFER; TRIS(2,2'-BIPYRIDINE)RUTHENIUM(II); REDOX CENTERS; NAFION MEMBRANE;
D O I
10.1016/0022-0728(95)03982-M
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Charge transfer between Ru(bpy):(2+)(3) (where bpy is 2,2'-bipyridine) complexes incorporated into a Nafion(R) membrane has been investigated using in situ spectrocyclic voltammetry and statistical calculation of the intermolecular distance between the complexes. The membrane was prepared either by a mixture casting method in which an alcoholic mixture solution of Nafion and the complex was cast to form a membrane, or by an adsorption method in which the complex was adsorbed from its aqueous solution into a precoated Nafion(R) membrane. It has been found that the electrochemical reactivity of the complex in a membrane prepared by the adsorption method is much higher than that prepared by the mixture casting method. The charge transfer distance between the complexes (R(0)) in the membrane prepared by the adsorption method was 1.6 nm (scan rate, 2 mV s(-1); pH 5.5), when assuming a random dispersion of the complex, which is significantly longer than that (1.1 nm) in the membrane prepared by the mixture casting method. The emission lifetime of the photoexcited Ru(bpy):(2+)(3) in the membrane suggests that the complex is localized in the membrane when it is prepared by an adsorption method; such localization would make the calculated R(0) value greater than the real value. The fraction of the volume in the membrane where the complex is adsorbed was estimated as 20 +/- 3%, by comparing the real local complex concentration in the membrane obtained from the R(0) value (1.1 nm) for the mixture casting system with the apparent average complex concentration.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 32 条
[1]   CONFINEMENT OF CHARGE-CARRIERS AND MOLECULAR EXCITONS WITHIN 5-NM-THICK EMITTER LAYER IN ORGANIC ELECTROLUMINESCENT DEVICES WITH A DOUBLE HETEROSTRUCTURE [J].
ADACHI, C ;
TSUTSUI, T ;
SAITO, S .
APPLIED PHYSICS LETTERS, 1990, 57 (06) :531-533
[2]   KINETICS OF ELECTRON-TRANSFER CROSS-REACTIONS WITHIN REDOX POLYMERS - COATINGS OF A PROTONATED POLYLYSINE CO-POLYMER WITH INCORPORATED ELECTROACTIVE ANIONS [J].
ANSON, FC ;
OHSAKA, T ;
SAVEANT, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (15) :4883-4890
[3]   OUTER-SPHERE OXIDATION OF ASCORBATE WITH OS(BPY)3(3+) INCORPORATED IN NAFION COATINGS ON GRAPHITE-ELECTRODES [J].
ANSON, FC ;
TSOU, YM ;
SAVEANT, JM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 178 (01) :113-127
[4]   SELF-EXCHANGE REACTIONS AT REDOX POLYMER ELECTRODES - A KINETIC-MODEL AND THEORY FOR STATIONARY VOLTAMMETRIC TECHNIQUES [J].
ANSON, FC ;
SAVEANT, JM ;
SHIGEHARA, K .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (02) :214-219
[5]   DYNAMICS OF ELECTRON HOPPING IN ASSEMBLIES OF REDOX CENTERS - PERCOLATION AND DIFFUSION [J].
BLAUCH, DN ;
SAVEANT, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (09) :3323-3332
[6]   EFFECTS OF LONG-RANGE ELECTRON-TRANSFER ON CHARGE-TRANSPORT IN STATIC ASSEMBLIES OF REDOX CENTERS [J].
BLAUCH, DN ;
SAVEANT, JM .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (24) :6444-6448
[7]   ELECTROCHEMICAL CONTROL OF THE LUMINESCENT LIFETIME OF RU(BPY)32+STAR INCORPORATED IN NAFION FILMS ON GRAPHITE-ELECTRODES [J].
BUTTRY, DA ;
ANSON, FC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (18) :4824-4829
[8]   EFFECTS OF ELECTRON EXCHANGE AND SINGLE-FILE DIFFUSION ON CHARGE PROPAGATION IN NAFION FILMS CONTAINING REDOX COUPLES [J].
BUTTRY, DA ;
ANSON, FC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (04) :685-689
[9]   CHARGE TRANSPORT BY ELECTRON EXCHANGE CROSS REACTION IN CYCLIC VOLTAMMETRY OF IRCL63(-)-FE(CN)63- MIXTURES TRAPPED IN POLYCATIONIC FILMS ON ELECTRODES [J].
FACCI, J ;
MURRAY, RW .
JOURNAL OF PHYSICAL CHEMISTRY, 1981, 85 (20) :2870-2873
[10]  
HABEL CT, 1989, J PHYS CHEM-US, V93, P1190