Formation of Bi2S3 thin films on Au(111) by electrochemical atomic layer epitaxy:: kinetics of structural changes in the initial monolayers

被引:39
作者
Öznülüer, T [1 ]
Demir, Ü [1 ]
机构
[1] Ataturk Univ, Fac Arts & Sci, Dept Chem, TR-25249 Erzurum, Turkey
关键词
electrochemical atomic layer epitaxy; Upd; Bi2S3; electrodeposition;
D O I
10.1016/S0022-0728(02)00921-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The kinetics and growth mechanism of the first and second monolayers of Bi2S3 by electrochemical atomic layer epitaxy (ECALE) has been studied using voltammetry and chronoamperometry techniques. Scan rate dependent cyclic voltammetry experiments reveal that the peak current in the stripping of the S layer from a Bi modified Au(111) electrode is a linear function of a 2/3 power of the scan rate, v(2/)3. Similar behavior is observed for the deposition of Bi on to one atomic layer of an S modified Au(111) electrode. The dissolution of the Bi atomic layer from the S modified Au(111) electrode involves an initial Langmuir-type adsorption-desorption accompanied by a nucleation and two-dimensional (2-D) growth process. When Bi atomic layers are used as a first layer, the nucleation and 2-D growth process was observed for both deposition and stripping. Analysis of the reduced variables demonstrates that the stripping of S from Au(111)-Bi and stripping of Bi from Au(111)-S fit the progressive model. Our results suggest that the nucleation and 2-D growth mechanism is the dominant process in the formation of Bi2S3 atomic layers if Bi is used as the first layer in the ECALE method. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:34 / 42
页数:9
相关论文
共 33 条
[1]   Electrochemical studies of the effects of pH and the surface structure of gold substrates on the underpotential deposition of sulfur [J].
Alanyalioglu, M ;
Çakal, H ;
Öztürk, AE ;
Demir, Ü .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (43) :10588-10593
[2]  
[Anonymous], ELECTROANALYTICAL CH
[3]   A KINETIC-MODEL OF MULTILAYER ADSORPTION IN ELECTROCHEMICAL PHASE FORMATION [J].
BARRADAS, RG ;
BOSCO, E .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1985, 193 (1-2) :23-26
[4]   KINETICS OF ELECTROCRYSTALLIZATION OF THIN FILMS OF CALOMEL [J].
BEWICK, A ;
THIRSK, HR ;
FLEISCHMANN, M .
TRANSACTIONS OF THE FARADAY SOCIETY, 1962, 58 (479) :2200-&
[5]  
BOSCO E, 1981, J ELECTROANAL CHEM, V129, P25, DOI 10.1016/S0022-0728(81)80003-4
[6]   ELECTRODEPOSITED BISMUTH MONOLAYERS ON AU(111) ELECTRODES - COMPARISON OF SURFACE X-RAY-SCATTERING, SCANNING-TUNNELING-MICROSCOPY, AND ATOMIC-FORCE MICROSCOPY LATTICE STRUCTURES [J].
CHEN, CH ;
KEPLER, KD ;
GEWIRTH, AA ;
OCKO, BM ;
WANG, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (28) :7290-7294
[7]   CORRELATION OF ELECTRODE SURFACE-STRUCTURE WITH ACTIVITY TOWARD H2O2 ELECTROREDUCTION FOR BI MONOLAYERS ON AU(111) [J].
CHEN, CH ;
GEWIRTH, AA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (13) :5439-5440
[8]   Formation of thin films of CdTe, CdSe, and CdS by electrochemical atomic layer epitaxy [J].
Colletti, LP ;
Flowers, BH ;
Stickney, JL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (05) :1442-1449
[9]   THIN-LAYER ELECTROCHEMICAL STUDIES OF THE OXIDATIVE UNDERPOTENTIAL DEPOSITION OF SULFUR AND ITS APPLICATION TO THE ELECTROCHEMICAL ATOMIC LAYER EPITAXY DEPOSITION OF CDS [J].
COLLETTI, LP ;
TEKLAY, D ;
STICKNEY, JL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 369 (1-2) :145-152
[10]   Electrochemistry of Cd at (root 3x root 3)R30 degrees-S/Au(111): Kinetics of structural changes in CdS monolayers [J].
Demir, U ;
Shannon, C .
LANGMUIR, 1996, 12 (25) :6091-6097