Structural, optical and DC conduction studies on vacuum evaporated Sr doped BaTiO3(BST) thin films prepared from Sr doped BaTiO3 nano particles

被引:0
作者
Sengodan, R. [1 ]
Shekar, B. Chandar [2 ]
机构
[1] Kumaraguru Coll Technol, Dept Phys, Coimbatore, Tamil Nadu, India
[2] Kongunadu Arts & Sci Coll, Dept Phys, Coimbatore, Tamil Nadu, India
来源
JOURNAL OF OPTOELECTRONICS AND ADVANCED MATERIALS | 2014年 / 16卷 / 5-6期
关键词
Barium strontium titanate; Thermal evaporation; XRD; UV; -; Visible; DC Conduction and Poole - Frenkel; SOL-GEL TECHNIQUE; BARIUM-TITANATE; ELECTRICAL-PROPERTIES; DIELECTRIC-PROPERTIES; PRECURSOR METHOD; TEMPERATURE; DEPOSITION; MECHANISM; (BA;
D O I
暂无
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Barium titanate (BaTiO3) doped with Strontium (BST) nanoparticles prepared by using wet chemical method were thermally evaporated on to well cleaned glass substrates under the vacuum of 2 x 10(-5) torr, using 12A4 Hind Hivac coating unit. The structure, optical and electrical properties of the deposited BST thin films were studied using the X-ray diffraction (XRD), optical transmittance and current voltage measurements. The thickness of the film was measured by quartz crystal monitor. From X-ray analysis, it has been found that BaTiO3 nanoparticles possess tetragonal structure and the deposited films were polycrystalline in nature, whereas the crytstallinity increases with increase of thickness. The extinction coefficient of the BST thin films decreases and on the other hand, refractive index increases with increasing thickness. The optical band gap energy value decreases with increase of film thickness. In the DC conduction studies, the Current-Voltage characteristics of the films showed ohmic conduction in the low field region. The conduction mechanism was found to be Poole-Frenkel at high field region. The activation energy values were estimated and were found to be decreasing with increasing applied field. The zero field value of the activation energy was found to be 0.28 eV.
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页码:554 / 561
页数:8
相关论文
共 35 条
[1]   Dielectric Thin Film from Barium Titanate Nanopowders [J].
Aal, A. Abdel ;
Rashad, M. M. ;
Amin, G. A. .
PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON NANOSCIENCE AND TECHNOLOGY, 2007, 61 :1-5
[2]   EFFECT OF PARTICLE-SIZE ON THE ROOM-TEMPERATURE CRYSTAL-STRUCTURE OF BARIUM-TITANATE [J].
BEGG, BD ;
VANCE, ER ;
NOWOTNY, J .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1994, 77 (12) :3186-3192
[3]   COMPARATIVE-STUDY OF AMORPHOUS AND CRYSTALLINE (BA, SR)TIO3 THIN-FILMS DEPOSITED BY LASER-ABLATION [J].
BHATTACHARYA, P ;
KOMEDA, T ;
PARK, K ;
NISHIOKA, Y .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 1993, 32 (9B) :4103-4106
[4]  
Boulos M., SOLID STATE IONICS, V176, P1301
[5]   PREPARATION AND OPTICAL-PROPERTIES OF CD1-XZNXTE FILMS [J].
CHATTOPADHYAY, KK ;
SARKAR, A ;
CHAUDHURI, S ;
PAL, AK .
VACUUM, 1991, 42 (17) :1113-1116
[6]   Microstructure, dielectric properties and hydrogen gas sensitivity of sputtered amorphous Ba0.67Sr0.33TiO3 thin films [J].
Chen, XF ;
Zhu, WG ;
Tan, OK .
MATERIALS SCIENCE AND ENGINEERING B-SOLID STATE MATERIALS FOR ADVANCED TECHNOLOGY, 2000, 77 (02) :177-184
[7]   Si monolithic microbolometers of ferroelectric BST thin film combined with readout FET for uncooled infrared image sensor [J].
Hashimoto, K ;
Xu, HP ;
Mukaigawa, T ;
Kubo, R ;
Zhu, H ;
Noda, M ;
Okuyama, M .
SENSORS AND ACTUATORS A-PHYSICAL, 2001, 88 (01) :10-19
[8]   Effects of thickness on the infrared optical properties of Ba0.9Sr0.1TiO3 ferroelectric thin films [J].
Hu, Z ;
Wang, G ;
Huang, Z ;
Meng, X ;
Zhao, Q ;
Chu, J .
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2004, 78 (05) :757-760
[9]   Structure-related infrared optical properties of BaTiO3 thin films grown on Pt/Ti/SiO2/Si substrates [J].
Hu, ZG ;
Wang, GS ;
Huang, ZM ;
Chu, JH .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2003, 64 (12) :2445-2450
[10]   Infrared optical properties of Ba0.8Sr0.2TiO3 ferroelectric thin films [J].
Huang, ZM ;
Zhang, ZH ;
Jiang, CP ;
Yu, JA ;
Sun, JL ;
Chu, JH .
APPLIED PHYSICS LETTERS, 2000, 77 (22) :3651-3653