Mechanism of reductive oxygen adsorption on active carbons with various surface chemistry

被引:166
作者
Strelko, VV
Kartel, NT
Dukhno, IN
Kuts, VS
Clarkson, RB
Odintsov, BM
机构
[1] NAS Ukraine, Inst Sorpt & Problems Endoecol, UA-03164 Kiev, Ukraine
[2] Univ Illinois, Dept Vet Clin Med, Urbana, IL 61801 USA
[3] Univ Illinois, Biomed Imaging Ctr, Urbana, IL 61801 USA
[4] Russian Acad Sci, Inst Radio Engn & Elect, Moscow 103907, Russia
基金
美国国家卫生研究院;
关键词
carbon; surface electronic phenomena (work function; surface potential; surface states; etc.); surface chemical reaction; polycrystalline surfaces; clusters; chemisorption; oxygen; porous solids;
D O I
10.1016/j.susc.2003.11.012
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
With the use of a semi-empirical quantum chemical method AM1, it is shown that the availability of 4-6% oxygen heteroatoms of furan- and pyrone-type, and/or also 2-3% N of pyrrol-type in a carbon matrix should provide greatest electron-donor ability to carbons. The synthetic carbons HPSC and SCN, containing various states and amounts of O- and N-heteroatoms, were prepared and analyzed to confirm this prediction experimentally. Utilizing an electrochemical cell with divided electrode spaces, the reduction processes of a series of strong oxidizers and 02 (on a spongy platinum electrode) in synthetic carbons with various surface chemical compositions were investigated directly by measuring a current in an external circuit. A good correlation between calculated data and electrochemical measurements was obtained. Two mechanisms of chemisorption of oxygen on evacuated carbons are suggested: homolytic (free radical) at small degrees of filling of a surface by oxygen, and heterolytic (at large degrees of filling) causing the fixation of oxygen on a surface in the form of a superoxide-ion O*(2-). (C) 2003 Published by Elsevier B.V.
引用
收藏
页码:281 / 290
页数:10
相关论文
共 18 条
[1]   SURFACE-CHEMISTRY OF CARBON - ACTIVATION OF MOLECULAR-OXYGEN [J].
ATAMNY, F ;
BLOCKER, J ;
DUBOTZKY, A ;
KURT, H ;
TIMPE, O ;
LOOSE, G ;
MAHDI, W ;
SCHLOGL, R .
MOLECULAR PHYSICS, 1992, 76 (04) :851-886
[2]  
Bansal R.C., 1988, ACTIVE CARBON
[3]   THE REACTION OF CARBON WITH HYDROGEN AT HIGH PRESSURE [J].
BLACKWOOD, JD .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1959, 12 (01) :14-28
[4]   BASIC SURFACE OXIDES ON CARBON .1. ADSORPTION OF ACIDS [J].
BOEHM, HP ;
VOLL, M .
CARBON, 1970, 8 (02) :227-&
[5]   Electron paramagnetic resonance and dynamic nuclear polarization of char suspensions: surface science and oximetry [J].
Clarkson, RB ;
Odintsov, BM ;
Ceroke, PJ ;
Ardenkjaer-Larsen, JH ;
Fruianu, M ;
Belford, RL .
PHYSICS IN MEDICINE AND BIOLOGY, 1998, 43 (07) :1907-1920
[6]   Regarding the adsorption of electrolytes through activated carbon [J].
Frumkin, A .
KOLLOID-ZEITSCHRIFT, 1930, 51 (01) :123-129
[7]   Redox characterization of furnace carbon black surfaces [J].
Goeringer, S ;
de Tacconi, NR ;
Chenthamarakshan, CR ;
Rajeshwar, K ;
Wampler, WA .
CARBON, 2001, 39 (04) :515-522
[8]  
Kuts VS, 2002, NATO SCI SER II MATH, V61, P635
[9]  
LEON CALY, 1994, CHEM PHYS CARBON, V24, P213
[10]   On the modification and characterization of chemical surface properties of activated carbon: In the search of carbons with stable basic properties [J].
Menendez, JA ;
Phillips, J ;
Xia, B ;
Radovic, LR .
LANGMUIR, 1996, 12 (18) :4404-4410