Effect of total gas and oxygen partial pressure during deposition on the properties of sputtered V2O5 thin films

被引:30
作者
Gies, A
Pecquenard, B
Benayad, A
Martinez, H
Gonbeau, D
Fuess, H
Levasseur, A
机构
[1] Univ Bordeaux 1, CNRS, Inst Chim Mat Condensee Bordeaux, F-33608 Pessac, France
[2] Univ Bordeaux 1, Ecole Normale Super Chim & Phys Bordeaux, F-33608 Pessac, France
[3] CNRS, UMR 5624, LCTPCM, F-64053 Pau, France
[4] Tech Univ Darmstadt, Dept Mat Sci, D-64287 Darmstadt, Germany
关键词
vanadium pentoxide; sputtering; thin films; lithium microbatteries;
D O I
10.1016/j.ssi.2005.02.012
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
Amorphous and crystalline vanadium pentoxide thin films have been deposited by rf magnetron sputtering in a pure argon or mixed argon/oxygen atmosphere using a V2O5 target with no intentional heating of the substrate. The effect of the total gas pressure and/or the oxygen partial pressure on the deposition rate, the composition, the structure, the surface morphology and the electrochemical properties of the films were investigated. The films were characterized by various methods such as X-ray Photoelectron Spectroscopy, Auger Electron Spectroscopy, XRD, Raman spectroscopy and SEM. The electrochemical performances have been evaluated by galvanostatic cycling. Thin films prepared in absence of oxygen or at a low oxygen partial pressure (10%) are amorphous and dense with a smooth surface, whatever the total pressure. In contrast, thin films prepared at an oxygen partial pressure higher than 10% are crystallized and mainly porous, the increase of the total pressure leading to a more pronounced preferential orientation with the c-axis perpendicular to the substrate. The best electrochemical results in terms of discharge capacity values are obtained for thin films prepared under a high total gas pressure. Moreover, dense thin films with a smooth surface are all showing a good cycling stability. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1627 / 1634
页数:8
相关论文
共 30 条
[1]   VIBRATIONAL-SPECTRA AND VALENCE FORCE-FIELD OF CRYSTALLINE V2O5 [J].
ABELLO, L ;
HUSSON, E ;
REPELIN, Y ;
LUCAZEAU, G .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1983, 39 (07) :641-651
[2]   Thin-film lithium and lithium-ion batteries [J].
Bates, JB ;
Dudney, NJ ;
Neudecker, B ;
Ueda, A ;
Evans, CD .
SOLID STATE IONICS, 2000, 135 (1-4) :33-45
[3]   THIN-FILM RECHARGEABLE LITHIUM BATTERIES [J].
BATES, JB ;
DUDNEY, NJ ;
LUBBEN, DC ;
GRUZALSKI, GR ;
KWAK, BS ;
YU, XH ;
ZUHR, RA .
JOURNAL OF POWER SOURCES, 1995, 54 (01) :58-62
[4]  
Bates JB, 2000, NEW TRENDS ELECTROCH, V1, P453
[5]   THE LIXV2O5 SYSTEM - AN OVERVIEW OF THE STRUCTURE MODIFICATIONS INDUCED BY THE LITHIUM INTERCALATION [J].
DELMAS, C ;
COGNACAURADOU, H ;
COCCIANTELLI, JM ;
MENETRIER, M ;
DOUMERC, JP .
SOLID STATE IONICS, 1994, 69 (3-4) :257-264
[6]   OMEGA-LIXV2O5 - A NEW ELECTRODE MATERIAL FOR RECHARGEABLE LITHIUM BATTERIES [J].
DELMAS, C ;
BRETHES, S ;
MENETRIER, M .
JOURNAL OF POWER SOURCES, 1991, 34 (02) :113-118
[7]   Mixed-valence vanadium oxides studied by XPS [J].
Demeter, M ;
Neumann, M ;
Reichelt, W .
SURFACE SCIENCE, 2000, 454 (01) :41-44
[8]   XPS analysis of new lithium cobalt oxide thin-films before and after lithium deintercalation [J].
Dupin, JC ;
Gonbeau, D ;
Benqlilou-Moudden, H ;
Vinatier, P ;
Levasseur, A .
THIN SOLID FILMS, 2001, 384 (01) :23-32
[9]   A REFINEMENT OF THE STRUCTURE OF V2O5 [J].
ENJALBERT, R ;
GALY, J .
ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 1986, 42 :1467-1469
[10]   Synthesis and structural, electrochromic characterization of pulsed laser deposited vanadium oxide thin films [J].
Fang, GJ ;
Liu, ZL ;
Wang, Y ;
Liu, YH ;
Yao, KL .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 2001, 19 (03) :887-892