Up-conversion luminescence and temperature sensing properties in Er-doped ferroelectric Sr2Bi4Ti5O18

被引:36
作者
Wei, T. [1 ]
Dong, Z. [1 ]
Zhao, C. Z. [2 ]
Ma, Y. J. [1 ]
Zhang, T. B. [1 ]
Xie, Y. F. [1 ]
Zhou, Q. J. [1 ]
Li, Z. P. [1 ]
机构
[1] Civil Aviat Univ China, Coll Sci, Tianjin 300300, Peoples R China
[2] Tianjin Polytech Univ, Sch Elect & Informat Engn, Tianjin 300160, Peoples R China
基金
中国国家自然科学基金;
关键词
Bismuth layer-structured ferroelectric; Ferroelectric; Up-conversion luminescence; ENERGY-TRANSFER; PHOTOLUMINESCENCE; NANOPARTICLES; EMISSIONS; PHOSPHOR; GLASSES; RAMAN; YB3+; TB; EU;
D O I
10.1016/j.ceramint.2015.12.121
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Er-doped Sr2Bi4Ti5O18 (SBT-x) ceramics were synthesized via a solid-state reaction method, and their structure, up-conversion luminescence (UCL), temperature sensing performance and ferroelectric behaviors were investigated. The obtained SBT-x samples crystallize in the polar orthorhombic phase, with space group B2cb. Under 980 nm excitation, bright green and weak red emissions are observed which correspond to the transitions from 2H(11/2)/S-4(3/2) and F-4(9/2) to I-4(15/2) level, respectively. The optimal doping concentration of Er3+ in SBT host is determined as 0.08. The critical energy transfer distance (R-c) is about 20.57 angstrom and the major interaction mechanism among Er3+ ions is determined as the d-d interaction. A possible UCL mechanism is proposed in light of the dependence of emission intensities on pumping power. Furthermore, optical temperature sensing properties are also investigated according to the fluorescence intensity ratio (FIR) of green emissions at 527 and 550 nm in the temperature range from 303 K to 573 K. The maximum sensing sensitivity is found to be 0.0042 K-1. Additionally, the response of SBT-x to external electric field stimuli is also confirmed. It is believed that SBT-x has potential application as optical temperature sensing materials. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:5537 / 5545
页数:9
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