The effect of the cooling atmosphere in the preparation of flame-annealed Pt(111) electrodes on CO adlayer oxidation

被引:75
作者
Lebedeva, NP [1 ]
Koper, MTM
Feliu, JM
van Santen, RA
机构
[1] Eindhoven Univ Technol, Schuit Inst Catalysis, Inorgan Chem & Catalysis Lab, NL-5600 MB Eindhoven, Netherlands
[2] Univ Alicante, Dept Quim Fis, E-03080 Alicante, Spain
关键词
carbon monoxide; Pt(111); crystalline defects; oxidation;
D O I
10.1016/S1388-2481(00)00062-X
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effect of the cooling atmosphere on the rate of CO adlayer oxidation on flame-annealed Pt( 111) has been studied. Cooling of a flame-annealed Pt(111) electrode in air results in a higher amount of crystalline defects compared to Pt(111) cooled in a hy-drogen-argon stream. Although the blank profiles in 0.5 M H2SO4 of Pt(111), cooled in air and under oxygen exclusion, are virtually identical, CO adlayer oxidation occurs at significantly lower overpotentials on the former electrode. Three voltammetric peaks are observed for subsaturated CO adlayer oxidation on Pt(111), cooled in Ar+H-2 mixture, while only two peaks develop in the case of a Pt(111) surface cooled in air. Random crystalline defects, introduced via cooling of a flame-annealed Pt(111) in air, enhance CO adlayer oxidation, and apparently also suppress the third high-potential peak observed on a quasi-perfect (111) surface. The high sensitivity of the saturated CO adlayer oxidation to the presence of crystalline defects on Pt(111) can hence be used as a straightforward, sensitive, though qualitative method to assess the degree of crystalline order of the electrode. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:487 / 490
页数:4
相关论文
共 24 条
[1]   Study of carbon monoxide adsorption and oxidation on Pt(111) by using an electrochemical impinging jet cell [J].
Bergelin, M ;
Feliu, JM ;
Wasberg, M .
ELECTROCHIMICA ACTA, 1998, 44 (6-7) :1069-1075
[2]   PREPARATION OF MONO-CRYSTALLINE PT MICROELECTRODES AND ELECTROCHEMICAL STUDY OF THE PLANE SURFACES CUT IN THE DIRECTION OF THE (111) AND (110) PLANES [J].
CLAVILIER, J ;
FAURE, R ;
GUINET, G ;
DURAND, R .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1980, 107 (01) :205-209
[3]   ELECTROCHEMICAL MONITORING OF THE THERMAL REORDERING OF PLATINUM SINGLE-CRYSTAL SURFACES AFTER METALLOGRAPHIC POLISHING FROM THE EARLY STAGE TO THE EQUILIBRIUM SURFACES [J].
CLAVILIER, J ;
ELACHI, K ;
PETIT, M ;
RODES, A ;
ZAMAKHCHARI, MA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1990, 295 (1-2) :333-356
[4]   ELECTROCHEMICAL ADSORPTION BEHAVIOR OF PLATINUM STEPPED SURFACES IN SULFURIC-ACID-SOLUTIONS [J].
CLAVILIER, J ;
ARMAND, D ;
SUN, SG ;
PETIT, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 205 (1-2) :267-277
[5]   ROLE OF ANION ON THE ELECTROCHEMICAL-BEHAVIOR OF A (111) PLATINUM SURFACE - UNUSUAL SPLITTING OF THE VOLTAMMOGRAM IN THE HYDROGEN REGION [J].
CLAVILIER, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1980, 107 (01) :211-216
[6]   ELECTROCHEMICAL STUDY OF THE INITIAL SURFACE CONDITION OF PLATINUM SURFACES WITH (100) AND (111) ORIENTATIONS [J].
CLAVILIER, J ;
ARMAND, D ;
WU, BL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1982, 135 (01) :159-166
[7]   Comparative evaluation of surface structure specificity of kinetics of UPD and OPD of H at single-crystal Pt electrodes [J].
Conway, BE ;
Barber, J ;
Morin, S .
ELECTROCHIMICA ACTA, 1998, 44 (6-7) :1109-1125
[8]   ELECTROCHEMICAL STUDIES IN SULFURIC-ACID-SOLUTIONS OF ABSORBED CO ON PT (111) ELECTRODES [J].
FELIU, JM ;
ORTS, JM ;
FERNANDEZVEGA, A ;
ALDAZ, A ;
CLAVILIER, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1990, 296 (01) :191-201
[9]   Anion adsorption from sulfuric acid solutions on Pt(111) single crystal electrodes [J].
Funtikov, AM ;
Stimming, U ;
Vogel, R .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1997, 428 (1-2) :147-153
[10]   Dependence of the potential of zero charge of stepped platinum (111) electrodes on the oriented step-edge density:: Electrochemical implications and comparison with work function behavior [J].
Gómez, R ;
Climent, V ;
Feliu, JM ;
Weaver, MJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (03) :597-605