Growth and characterization of ultrathin TiO2-Cr2O3 nanocomposite films

被引:15
作者
Dutta, Shankar [1 ]
Pandey, Akhilesh [1 ]
Leeladhar [1 ]
Jain, K. K. [1 ]
机构
[1] DRDO, Solid State Phys Lab, Lucknow Rd, Delhi 110054, India
关键词
Oxide materials; Vapor deposition; Thin films; X-ray diffraction; Optical spectroscopy; THIN-FILMS; SOL-GEL; SENSING PROPERTIES; VAPOR-DEPOSITION; TIO2; FILMS; GAS SENSOR; CR2O3; SPECTROSCOPY; OXIDE;
D O I
10.1016/j.jallcom.2016.11.284
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
This paper presents growth of TiO2-Cr2O3 nanocomposite ultrathin films (similar to 30 nm thick) by sputtering technique for gas sensor applications. The deposited films were annealed to grow rutile TiO2 and eskolaite Cr2O3 phases. Grain sizes of the pristine Cr2O3 and TiO2 films (45-50 nm) were found to be larger compared to the nano-composite (7.1-69.5% Cr2O3 in TiO2) films (15-40 nm). The Raman spectra of the pristine TiO2 film showed peaks at 220 cm(-1)(B(1)g), 435 cm(-1) (Eg) and 610 cm(-1) (A(1)g) are attributed to the rutile phase of TiO2. The pristine eskolaite Cr2O3 layer exhibited four Eg peaks at 300 cm(-1), 350 cm(-1), 520 cm(-1) and 620 cm(-1) along with the characteristic intense peak at 551 cm(-1) (A(1)g mode). The peak positions of the A(1)g mode (Cr2O3) and Eg mode (TiO2) are found to be red shifted from its characteristic peak positions; but no shift is detected due to the intermixing of Cr2O3 and TiO2 phases. However, the FWHM of the A(1)g mode is found to be increased from 9 cm(-1) (pristine Cr2O3) to 13 cm(-1) (26.1% Cr2O3); while the Eg mode is found to be increased from 48 cm(-1) (pristine TiO2) to 80 cm(-1) (46.9% Cr2O3) due nanocomposite formation between the rutile and eskolaite phases. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:376 / 381
页数:6
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