Scanning electrochemical microscopy Part 39. The proton/hydrogen mediator system and its application to the study of the electrocatalysis of hydrogen oxidation

被引:117
作者
Zhou, JF [1 ]
Zu, YB [1 ]
Bard, AJ [1 ]
机构
[1] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 2000年 / 491卷 / 1-2期
基金
美国国家科学基金会;
关键词
SECM; H-2; oxidation; electrocatalysis;
D O I
10.1016/S0022-0728(00)00100-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The H+/H-2, redox couple was investigated as a mediator system for scanning electrochemical microscopy (SECM) with proton reduction from a 0.01 M HClO4 solution at a Pt tip. The feedback behavior of the mediator was examined at different substrates (Pt, Au). Unlike the one-electron outer-sphere redox couples usually used as mediators in SECM, this mediator system is sensitive to the catalytic activity of the substrate surface for hydrogen oxidation rather than the conductivity of the substrate. The catalytic oxidation of H-2 on Pt was studied during cyclic voltammetric scans of the Pt substrate with a tip close to the substrate, and the inhibition by oxygen adsorption on Pt was investigated. The quantitative H-2 oxidation rate was determined at different substrate potentials from SECM approach curves. The kinetic parameters for proton reduction and hydrogen oxidation were determined by steady-state SECM voltammograms. The inhibitory effect of anions (Br-, I-) and reduction products of NO3- for catalytic H-2 oxidation on the Pt surface was also examined. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:22 / 29
页数:8
相关论文
共 30 条
[1]  
ANGERSTE.H, 1973, J ELECTROANAL CHEM, V43, P9, DOI 10.1016/0368-1874(73)80226-6
[2]   INVESTIGATION OF HYDROGEN IONIZATION ON PLATINUM WITH HELP OF MICROELECTRODES [J].
BAGOTZKY, VS ;
OSETROVA, NV .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1973, 43 (02) :233-249
[3]   Specificity of the kinetics of H2, evolution to the structure of single-crystal Pt surfaces, and the relation between opd and upd H [J].
Barber, J ;
Morin, S ;
Conway, BE .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 446 (1-2) :125-138
[4]  
Bard A.J., 1994, ELECTROANAL CHEM, V18, A., P243
[5]   SPECTROSCOPIC AND ELECTROCHEMICAL STUDIES OF IODINE COORDINATED TO NOBLE-METAL ELECTRODE SURFACES [J].
BERRY, GM ;
BOTHWELL, ME ;
BRAVO, BG ;
CALI, GJ ;
HARRIS, JE ;
MEBRAHTU, T ;
MICHELHAUGH, SL ;
RODRIGUEZ, JF ;
SORIAGA, MP .
LANGMUIR, 1989, 5 (03) :707-713
[6]   LIMITING OXYGEN COVERAGE ON PLATINIZED PLATINUM - RELEVANCE TO DETERMINATION OF REAL PLATINUM AREA BY HYDROGEN ADSORPTION [J].
BIEGLER, T ;
RAND, DAJ ;
WOODS, R .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1971, 29 (02) :269-&
[7]  
Bold W., 1961, Electrochim. Acta, V5, P145
[8]  
Breiter M. W., 1962, ELECTROCHIM ACTA, V7, P601
[9]  
Conway B.E., 1981, ELECTRODES CONDUCTIV, P433
[10]   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