ELECTROCHEMICAL ENHANCEMENT OF A CATALYTIC REACTION IN AQUEOUS-SOLUTION

被引:122
作者
NEOPHYTIDES, SG [1 ]
TSIPLAKIDES, D [1 ]
STONEHART, P [1 ]
JAKSIC, MM [1 ]
VAYENAS, CG [1 ]
机构
[1] STONEHART ASSOCIATES INC,MADISON,CT 06443
关键词
D O I
10.1038/370045a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE rates of many heterogeneous catalytic reactions between gaseous adsorbates on metal surfaces supported on solid electrolytes can be increased by applying a potential to the metal(1-8). This phenomenon, which has been reported previously at temperatures of 250-750 degrees C, has been shown(9) to be due to the electrochemically induced spillover of ions from the support onto the catalyst surface; the ions then act as promoters for the catalytic reaction. Here we report that a similar effect can be observed in aqueous solution at ambient temperatures. We studied the oxidation of H-2 on a platinum/graphite electrode immersed in aqueous KOH. Application of a positive potential of 1-2 V to the Pt electrode increased the rate of H-2 oxidation by up to 500%. We deduce that hydroxide ions are acting as promoters, and find that each ion supplied to the catalyst causes the oxidation of up to 20 hydrogen atoms. This kind of rate enhancement for heterogeneous catalytic reactions in solution may be of considerable technological value, for example in the electrochemical treatment of toxic organics(10) or the generation of useful industrial chemicals(4).
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页码:45 / 47
页数:3
相关论文
共 16 条
[1]   NON-FARADAIC ELECTROCHEMICAL MODIFICATION OF CATALYTIC ACTIVITY .1. THE CASE OF ETHYLENE OXIDATION ON PT [J].
BEBELIS, S ;
VAYENAS, CG .
JOURNAL OF CATALYSIS, 1989, 118 (01) :125-146
[2]  
Bockris J., 1973, MODERN ELECTROCHEMIS
[3]  
BOCKRIS JO, 1993, SURFACE ELECTROCHEMI, pCH3
[4]   ELECTROCHEMICAL MODIFICATION OF CH3OH OXIDATION SELECTIVITY AND ACTIVITY ON A PT SINGLE-PELLET CATALYTIC REACTOR [J].
CAVALCA, CA ;
LARSEN, G ;
VAYENAS, CG ;
HALLER, GL .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (23) :6115-6119
[5]   COMPARISONS BETWEEN COVERAGE-DEPENDENT INFRARED FREQUENCIES FOR CARBON-MONOXIDE ADSORBED ON ORDERED PT(111), PT(100), AND PT(110) IN ELECTROCHEMICAL AND ULTRAHIGH-VACUUM ENVIRONMENTS [J].
CHANG, SC ;
LEUNG, LWH ;
WEAVER, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (14) :5341-5345
[6]   BEHAVIOR AND CHARACTERIZATION OF KINETICALLY INVOLVED CHEMISORBED INTERMEDIATES IN ELECTROCATALYSIS OF GAS EVOLUTION REACTIONS [J].
CONWAY, BE ;
TILAK, BV .
ADVANCES IN CATALYSIS, 1992, 38 :1-147
[7]  
Conway BE, 1981, ELECTRODES CONDUCTIV
[8]   ORIGIN OF NON-FARADAIC ELECTROCHEMICAL MODIFICATION OF CATALYTIC ACTIVITY [J].
LADAS, S ;
KENNOU, S ;
BEBELIS, S ;
VAYENAS, CG .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (35) :8845-8848
[9]   THE EFFECT OF ELECTROCHEMICAL OXYGEN PUMPING ON THE RATE OF CO OXIDATION ON AU ELECTRODE-CATALYST [J].
MARINA, OA ;
SOBYANIN, VA .
CATALYSIS LETTERS, 1992, 13 (1-2) :61-69
[10]  
Plattner E., 1988, PROCESS TECHNOLOGIES, P205