Excitability and multistability in the electrochemical oxidation of primary alcohols

被引:22
作者
Chen, SL [1 ]
Schell, M [1 ]
机构
[1] So Methodist Univ, Dept Chem, Dallas, TX 75275 USA
基金
美国国家科学基金会;
关键词
excitability; oscillations; bistability; ethanol; 1-butanol;
D O I
10.1016/S0013-4686(00)00393-5
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Results are presented from experiments on the electrocatalyzed oxidation of I-butanol at a Pt electrode conducted under conditions of constant current in both acid and NaOH solutions. Several nonlinear behaviors are characterized. In acid solution, the oxidation of I-butanol exhibits excitability, i.e. a small perturbation induces a large amplitude excursion with mixed time scales before the system returns to stationary behavior. It is argued that excitability reveals that oxides directly partake in the oxidation process. Butanol oxidation also exhibits a tristable response in acid solution in which three different stationary states exist under the same conditions. A different tristability also occurs in which an oscillatory state coexists with two stationary states. Instead of a tristable response, the oxidation of 1-butanol displays a bistable response in NaOH solution. Results are compared with those obtained for alcohols with a smaller number of carbon atoms, ethanol and methanol. In view of results from potential controlled experiments, the results of the current controlled experiments reveal what can be considered nonintuitive current-potential relations. Relations among the observed nonlinear behaviors, current-potential relations, and mechanisms, as well as the differences between results obtained in NaOH solution and those obtained in acid solution are discussed. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3069 / 3080
页数:12
相关论文
共 36 条
[1]  
[Anonymous], OSCILLATIONS TRAVELI
[2]   INSITU ANALYSIS BY INFRARED REFLECTANCE SPECTROSCOPY OF THE ADSORBED SPECIES RESULTING FROM THE ELECTROSORPTION OF ETHANOL ON PLATINUM IN ACID-MEDIUM [J].
BEDEN, B ;
MORIN, MC ;
HAHN, F ;
LAMY, C .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 229 (1-2) :353-366
[3]   VOLTAMMETRIC AND CHRONOPOTENTIOMETRIC STUDY OF THE ANODIC OXIDATION OF METHANOL, FORMALDEHYDE, AND FORMIC ACID [J].
BUCK, RP ;
GRIFFITH, LR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1962, 109 (11) :1005-1013
[4]   METAL CRYSTALLINITY EFFECTS IN ELECTROCATALYSIS AS PROBED BY REAL-TIME FTIR SPECTROSCOPY - ELECTROOXIDATION OF FORMIC-ACID, METHANOL, AND ETHANOL ON ORDERED LOW-INDEX PLATINUM SURFACES [J].
CHANG, SC ;
LEUNG, LWH ;
WEAVER, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (15) :6013-6021
[5]   Bistability and excitability in the electrochemical oxidation of ethanol [J].
Chen, SL ;
Schell, M .
ELECTROCHIMICA ACTA, 1999, 44 (26) :4773-4780
[6]   NEW APPROACHES TO STUDY OF ELECTROCHEMICAL DECARBOXYLATION AND KOLBE REACTION .1. MODEL REACTION WITH FORMATE [J].
CONWAY, BE ;
DZIECIUCH, M .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1963, 41 (01) :21-&
[7]   CHARACTERIZATION OF ELECTROCATALYSIS IN THE OXYGEN EVOLUTION REACTION AT PLATINUM BY EVALUATION OF BEHAVIOR OF SURFACE INTERMEDIATE STATES AT THE OXIDE FILM [J].
CONWAY, BE ;
LIU, TC .
LANGMUIR, 1990, 6 (01) :268-276
[8]   A SURFACE-ELECTROCHEMICAL BASIS FOR THE DIRECT LOGARITHMIC GROWTH LAW FOR INITIAL-STAGES OF EXTENSION OF ANODIC OXIDE-FILMS FORMED AT NOBLE-METALS [J].
CONWAY, BE ;
BARNETT, B ;
ANGERSTEINKOZLOWSKA, H ;
TILAK, BV .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (11) :8361-8373
[9]   MECHANISMS OF FORMIC-ACID, METHANOL, AND CARBON-MONOXIDE ELECTROOXIDATION AT PLATINUM AS EXAMINED BY SINGLE POTENTIAL ALTERATION INFRARED-SPECTROSCOPY [J].
CORRIGAN, DS ;
WEAVER, MJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 241 (1-2) :143-162
[10]   METHANOL ELECTROOXIDATION ON WELL-CHARACTERIZED PT-RN ALLOYS [J].
GASTEIGER, HA ;
MARKOVIC, N ;
ROSS, PN ;
CAIRNS, EJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (46) :12020-12029