Preparation of nm-sized BaTiO3 crystallites by a LTDS method using a highly concentrated aqueous solution

被引:83
作者
Wada, S
Tsurumi, T
Chikamori, H
Noma, T
Suzuki, T
机构
[1] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Met & Ceram Sci, Meguro Ku, Tokyo 1528552, Japan
[2] Tokyo Univ Agr & Technol, Dept Appl Chem, Koganei, Tokyo 1848558, Japan
关键词
crystallites; defects; growth from solutions; barium compounds; nanomaterials; dielectric materials;
D O I
10.1016/S0022-0248(01)01198-8
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
A low temperature direct synthesis method is useful for preparing nm-sized barium titanate (BaTiO3) crystallites, However, its characterization revealed that in BaTiO3 crystallites prepared by this method, there were many hydroxyl groups and barium vacancies. This is because of the use of aqueous solutions as starting materials. To prepare BaTiO3 crystallites with a hydroxyl group less, use of a highly concentrated aqueous solution must be required. In this study, BaTiO3 crystallites were prepared under a dry N-2 atmosphere using the highly concentrated aqueous solution. As a result, the formation of BaTiO3 crystallites with sizes around 16nm were confirmed. XRD and Raman measurements revealed that as-prepared powder was BaTiO3 single phase. However, in as-prepared BaTiO3 crystallites, a hydroxyl group was detected as an impurity. Its chemical analysis determined that the Ba/Ti atomic ratio was 0.786 +/- 0.005, which implies the presence of barium vacancies in the crystallites. The average crystal structure determined by XRD was assigned to a cubic m3m symmetry, while the local structure determined by Raman scattering was assigned to a tetragonal 4mm symmetry, which suggested that in the crystal structure of as-prepared BaTiO3 crystallites, there existed a disorder system. These crystallites were also characterized after annealing at various temperatures. (C) 2001 Elsevier Science B.V, All rights reserved.
引用
收藏
页码:433 / 439
页数:7
相关论文
共 18 条
[1]   DIELECTRIC-PROPERTIES OF FINE-GRAINED BARIUM-TITANATE CERAMICS [J].
ARLT, G ;
HENNINGS, D ;
DEWITH, G .
JOURNAL OF APPLIED PHYSICS, 1985, 58 (04) :1619-1625
[2]   A PHENOMENOLOGICAL GIBBS FUNCTION FOR BATIO3 GIVING CORRECT E-FIELD DEPENDENCE OF ALL FERROELECTRIC PHASE-CHANGES [J].
BELL, AJ ;
CROSS, LE .
FERROELECTRICS, 1984, 59 (3-4) :197-203
[3]  
Cullity B.D., 1978, ELEMENTS XRAY DIFFRA, V2nd, P102
[4]   Grain-size effect on structure and phase transformations for barium titanate [J].
Frey, MH ;
Payne, DA .
PHYSICAL REVIEW B, 1996, 54 (05) :3158-3168
[5]  
IKAWA H, 1993, DIELECTRIC CERAMICS, V32, P19
[6]   Size effect on the phase transition in PbTiO3 fine particles [J].
Ishikawa, K ;
Nomura, T ;
Okada, N ;
Takada, K .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 1996, 35 (9B) :5196-5198
[7]   SIZE EFFECT ON THE FERROELECTRIC PHASE-TRANSITION IN PBTIO3 ULTRAFINE PARTICLES [J].
ISHIKAWA, K ;
YOSHIKAWA, K ;
OKADA, N .
PHYSICAL REVIEW B, 1988, 37 (10) :5852-5855
[8]  
KAY HF, 1949, PHILOS MAG, V40, P1019
[9]   GRAIN-SIZE EFFECTS ON DIELECTRIC PROPERTIES IN BARIUM-TITANATE CERAMICS [J].
KINOSHITA, K ;
YAMAJI, A .
JOURNAL OF APPLIED PHYSICS, 1976, 47 (01) :371-373
[10]  
McCauley D, 1998, J AM CERAM SOC, V81, P979, DOI 10.1111/j.1151-2916.1998.tb02435.x