In-situ Electric Field-Induced Modulation of Photoluminescence in Pr-doped Ba0.85Ca0.15Ti0.90Zr0.10O3 Lead-Free Ceramics

被引:67
作者
Sun, Hai Ling [1 ]
Wu, Xiao [1 ]
Chung, Tat Hang [1 ]
Kwok, K. W. [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Appl Phys, Kowloon, Hong Kong, Peoples R China
关键词
UP-CONVERSION LUMINESCENCE; PIEZOELECTRIC PROPERTIES; PHASE; RED; NANOCRYSTALS; EMISSION; BLUE; INTENSITIES; STRAIN; GREEN;
D O I
10.1038/srep28677
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Luminescent materials with dynamic photoluminescence activity have aroused special interest because of their potential widespread applications. One proposed approach of directly and reversibly modulating the photoluminescence emissions is by means of introducing an external electric field in an in-situ and real-time way, which has only been focused on thin films. In this work, we demonstrate that real-time electric field-induced photoluminescence modulation can be realized in a bulk Ba0.85Ca0.15Ti0.90Zr0.10O3 ferroelectric ceramic doped with 0.2 mol% Pr3+, owing to its remarkable polarization reversal and phase evolution near the morphotropic phase boundary. Along with in-situ X-ray diffraction analysis, our results reveal that an applied electric field induces not only typical polarization switching and minor crystal deformation, but also tetragonal-to-rhombohedral phase transformation of the ceramic. The electric field-induced phase transformation is irreversible and engenders dominant effect on photoluminescence emissions as a result of an increase in structural symmetry. After it is completed in a few cycles of electric field, the photoluminescence emissions become governed mainly by the polarization switching, and thus vary reversibly with the modulating electric field. Our results open a promising avenue towards the realization of bulk ceramic-based tunable photoluminescence activity with high repeatability, flexible controllability, and environmental-friendly chemical process.
引用
收藏
页数:8
相关论文
共 48 条
[1]  
Adams DM, 2000, J PHYS CHEM B, V104, P6728, DOI 10.1021/jpc994457a
[2]  
[Anonymous], 2011, Angew. Chem., DOI DOI 10.1002/ANGE.201101374
[3]   Tuning the Luminescence of Phosphors: Beyond Conventional Chemical Method [J].
Bai, Gongxun ;
Tsang, Ming-Kiu ;
Hao, Jianhua .
ADVANCED OPTICAL MATERIALS, 2015, 3 (04) :431-462
[4]   Tuning of near-infrared luminescence of SrTiO3:Ni2+ thin films grown on piezoelectric PMN-PT via strain engineering [J].
Bai, Gongxun ;
Zhang, Yang ;
Hao, Jianhua .
SCIENTIFIC REPORTS, 2014, 4
[5]  
Blasse G., 1994, GEN INTRO LUMINESCEN, V1, DOI [10.1007/978-3-642-79017-1_1, DOI 10.1007/978-3-642-79017-1_1]
[6]  
Blasse G., 1994, Luminescent Materials, P91, DOI DOI 10.1007/978-3-642-79017-1_5
[7]  
Blasse G., 1976, STRUCTURE BONDING, V26
[8]  
Coey JMD, 2009, ADV PHYS, V58, P571, DOI 10.1080/00018730903363184
[9]   BIOLOGICAL IMAGING Beyond fluorescence [J].
Cohen, Bruce E. .
NATURE, 2010, 467 (7314) :407-408
[10]   Electric-field-induced phase-change behavior in (Bi0.5Na0.5)TiO3-BaTiO3-(K0.5Na0.5)NbO3: A combinatorial investigation [J].
Daniels, John E. ;
Jo, Wook ;
Roedel, Juergen ;
Honkimaeki, Veijo ;
Jones, Jacob L. .
ACTA MATERIALIA, 2010, 58 (06) :2103-2111