OPEN CIRCUIT POTENTIAL MEASUREMENTS WITH TI/TIO2 ELECTRODES

被引:45
作者
AVENA, MJ [1 ]
CAMARA, OR [1 ]
DEPAULI, CP [1 ]
机构
[1] NATL UNIV CORDOBA,FAC CIENCIAS QUIM,DEPT FIS QUIM,INST INVEST FISICOQUIM CORDOBA,SUCURSAL 16,RA-5016 CORDOBA,ARGENTINA
来源
COLLOIDS AND SURFACES | 1993年 / 69卷 / 04期
关键词
OPEN CIRCUIT POTENTIAL; SURFACE CHARGE; TITANIUM OXIDE; TI/TIO2; ELECTRODES; TRIPLE-LAYER MODEL;
D O I
10.1016/0166-6622(93)80003-X
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
The open circuit potential (OCP) vs pH response of Ti/TiO2 electrodes prepared by thermal and electrochemical oxidation of metallic titanium was measured in KNO3 aqueous solutions in order to establish whether the slopes of the OCP-pH curves can be used as a measure of the variation of surface potential (psi0) of TiO2 with the pH of the aqueous solution. For comparison purposes, psi0-pH slopes were also evaluated from surface charge-pH data obtained by acid-base potentiometric titrations of TiO2 dispersions. Ti/TiO2 electrodes showed a linear OCP-pH response in the range of pH 5-10 with slopes of -0.039 +/- 0.005 V pH-1. The OCP-pH dependence of Ti/TiO2 electrodes was lower than that predicted thermodynamically. According to the triple-layer model, used to describe the oxide/aqueous solution interface, the OCP-pH slopes obtained for Ti/TiO2 electrodes cannot be identified with the variation of psi0 with the pH. Calculations with this model indicated that neither the single nor the double extrapolation methods used to evaluate the intrinsic ionization constant of oxide surface sites render realistic values of these parameters for the TiO2 surface. The analysis of surface charge-pH data and the use of the triple-layer model to predict experimental values indicated that the psi0-pH slopes of TiO2 surfaces must be greater (in absolute magnitude) than 0.041 V pH-1.
引用
收藏
页码:217 / 228
页数:12
相关论文
共 33 条
[1]   OPEN-CIRCUIT POTENTIALS OF ZRO2 ELECTRODES [J].
ARDIZZONE, S ;
RADAELLI, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 269 (02) :461-469
[2]  
Baes Jr C. F., 1976, HYDROLYSIS CATIONS, P147
[3]   STUDIES OF DEFECT STRUCTURE OF NONSTOICHIOMETRIC RUTILE TIO2-X [J].
BLUMENTHAL, RN ;
BAUKUS, J ;
HIRTHE, WM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1967, 114 (2P1) :172-+
[4]   THE INFLUENCE OF COUNTERION ADSORPTION ON THE PSI-0/PH CHARACTERISTICS OF INSULATOR SURFACES [J].
BOUSSE, L ;
DEROOIJ, NF ;
BERGVELD, P .
SURFACE SCIENCE, 1983, 135 (1-3) :479-496
[5]   MOTT-SCHOTTKY PLOTS AND FLAT-BAND POTENTIALS FOR SINGLE-CRYSTAL RUTILE ELECTRODES [J].
COOPER, G ;
TURNER, JA ;
NOZIK, AJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1982, 129 (09) :1973-1977
[6]   ELECTROCHEMISORPTION OF HEXAHYDROXYPLATINATE(IV) ON THIN TITANIA FILMS [J].
DAVIDSON, MR ;
HOFLUND, GB ;
NIINISTO, L ;
LAITINEN, HA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 228 (1-2) :471-480
[7]   SURFACE-IONIZATION AND COMPLEXATION AT THE OXIDE-WATER INTERFACE .3. ADSORPTION OF ANIONS [J].
DAVIS, JA ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1980, 74 (01) :32-43
[8]   SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .1. COMPUTATION OF ELECTRICAL DOUBLE-LAYER PROPERTIES IN SIMPLE ELECTROLYTES [J].
DAVIS, JA ;
JAMES, RO ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 63 (03) :480-499
[9]   TEMPERATURE-DEPENDENCE OF THE ELECTRICAL DOUBLE-LAYER ON OXIDES - RUTILE AND HEMATITE [J].
FOKKINK, LGJ ;
DEKEIZER, A ;
LYKLEMA, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1989, 127 (01) :116-131
[10]  
FURLONG DN, 1980, STUDIES PHYSICAL THE, V11, P367