Current oscillatory phenomena based on redox reactions at a hanging mercury drop electrode (HMDE) in dimethyl sulfoxide

被引:25
作者
Islam, MM [1 ]
Okajima, T [1 ]
Ohsaka, T [1 ]
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Elect Chem, Midori Ku, Yokohama, Kanagawa 2268502, Japan
关键词
D O I
10.1021/jp046421a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A systematic and comprehensive study on cyclic voltammetric anodic current oscillation (CVACO) at a hanging mercury drop electrode (HMDE) was carded out for the redox reactions of molecular oxygen (02), nitrobenzene (NB), 1,4-dinitrobenzene (DNB), benzoquinone (BQ), 2,3,5,6-tetramethylbenzoquinone (TMBQ), benzophenone (BP), azobenzene (AB), 2,1,3-benzothiadiazole (BTD), 7,7,8,8-tetracyanoquinodimethane (TCNQ), methyl viologen dichloride (MV2+), and tris(2,2'-bipyridine)ruthenium(II) dichloride [Ru(bpY)(3)(2+)] in dimethyl sulfoxide (DMSO) solutions containing 0.1 M tetraethylammonium perchlorate (TEAP). From the electrocapillary curve (ECC) obtained using a dropping mercury electrode as well as the capacitance versus potential curves measured using electrochemical impedance technique, the value of the potential of zero charge (PZC) was estimated to be -0.27 V versus Ag\AgCl\NaCl (sat.) in a DMSO solution containing 0.1 M TEAP. CVACO was found to occur only for the redox couples (i.e., BP0/BP.-, O-2(0)/O2(.-), AB(0)/AB(.-), Ru(bPY)(3)(2+)/Ru(bpY)(3)(+), BTD0/BTD.-, NB0/NB.-, DNB0/DNB.-, DNB.-/DNB2-, TMBQ(0)/TMBQ(.-), MV2+/MV.+, and BQ(.-)/BQ(2-)) having the formal potentials (E-0' values) more negative than the PZC. CVACO was largely dependent on the concentrations of redox species and TEAP; for example, in the case of BTD the intensity of CVACO increased with increasing concentration, and CVACO ceased at high concentrations of TEAP ( greater than or equal to0.5 M). Furthermore, CVACO was not observed for the BQ(0)/BQ(.-) redox couple having E-0'(= -0.31 V) near the PZC, and a pronounced cathodic maximum was observed for the TCNQ(.-)/TCNQ(2-) redox couple with E-0' (= -0.16 V) more positive than the PZC. These observations and the factors governing the CVACO are discussed on the basis of the theory presented for the polarographic maxima of the first kind. The observed CVACO and the cathodic maximum obtained for the TCNQ(.-)/TCNQ(2-) redox couple could be explained in terms of the so-called streaming effect.
引用
收藏
页码:19425 / 19431
页数:7
相关论文
共 27 条
[1]   THEORY OF POLAROGRAPHIC MAXIMUM CURRENT .1. CONDITIONS FOR ONSET OF HYDRODYNAMIC INSTABILITY IN A LIQUID-METAL ELECTRODE SYSTEM [J].
AOGAKI, R ;
KITAZAWA, K ;
FUEKI, K ;
MUKAIBO, T .
ELECTROCHIMICA ACTA, 1978, 23 (09) :867-874
[2]   THEORY OF POLAROGRAPHIC MAXIMUM CURRENT .2. GROWTH OF DECAY-RATE OF ELECTROCHEMICAL AND HYDRODYNAMIC INSTABILITY [J].
AOGAKI, R ;
KITAZAWA, K ;
FUEKI, K ;
MUKAIBO, T .
ELECTROCHIMICA ACTA, 1978, 23 (09) :875-880
[3]   ELECTROCHEMICAL-BEHAVIOR OF 2-NITROBENZIDINE IN N,N-DIMETHYLFORMAMIDE [J].
ARAVAMUTHAN, S ;
KALIDAS, C ;
VENKATACHALAM, CS .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 171 (1-2) :293-301
[4]   ELECTRON SPIN RESONANCE AND POLAROGRAPHIC STUDIES OF RADICAL-ANIONS OF SOME NITROGEN- AND SULPHUR-CONTAINING HETEROCYCLIC MOLECULES [J].
ATHERTON, NM ;
OCKWELL, JN .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1967, (05) :771-&
[5]  
BARD AJ, 1980, ELECTROCHEMICAL METH
[6]  
BAUER HH, 1975, ELECTROANALYTICAL CH, V8, P169
[7]   THE INFLUENCE OF DISPROPORTIONATION OF THE ANION RADICAL ON THE ELECTROCHEMICAL REDUCTION OF 1,9-DIMETHYLDIBENZO[B,F]PENTALENE [J].
BECKER, JY ;
GINZBURG, G ;
WILLNER, I .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1980, 108 (03) :355-368
[8]  
Che Y, 1998, CHEM LETT, P97
[9]   ELECTROCHEMICAL REDUCTION OF 1,1,4,4-TETRAPHENYLBUTATRIENE [J].
CHEN, TYR ;
ANDERSON, MR ;
PETERS, DG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 222 (1-2) :257-270
[10]  
DELEVIE R, 1965, J ELECTROANAL CHEM, V9, P331