Redox-induced dual optical switching of CaTiO3:Pr3+ phosphor nanoparticles synthesized by sol-gel method

被引:3
作者
Takahashi, Hideaki [1 ]
Hagiwara, Manabu [1 ]
Fujihara, Shinobu [1 ]
机构
[1] Keio Univ, Fac Sci & Technol, Dept Appl Chem, Kohoku Ku, 3-14-1 Hiyoshi, Yokohama, Kanagawa 2238522, Japan
关键词
CaTiO3:Pr3+; Phosphors; Nanoparticles; Photoluminescence; Optical switching; Redox reaction; ELECTRONIC-STRUCTURE; LUMINESCENCE; PHOTOLUMINESCENCE; MICROSPHERES; ENHANCEMENT; AFTERGLOW;
D O I
10.1007/s10971-022-05791-3
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
Red-emitting CaTiO3:Pr3+ phosphor nanoparticles were synthesized by a sol-gel method with a final heat treatment at a low temperature of 650 degrees C. For comparison, the CaTiO3:Pr3+ phosphor was also synthesized by a conventional solid-state reaction method conducted at 1250 degrees C. The two kinds of resultant CaTiO3:Pr3+ samples were revealed to differ largely in their microstructure and optical properties. Diffuse reflectance and photoluminescence measurements suggested that the sample from the solid-state reaction possessed a larger number of defects, which would deteriorate the optical properties, due to heating at high temperature. On the other hand, the sol-gel-derived sample exhibited much better optical properties and thus it was used for evaluating optical-switching phenomena upon redox treatments. In photoluminescence, three excitation bands were observed at 265, 335, and 375 nm for the red emission of the CaTiO3:Pr3+ sample, and one of them (375 nm) was more effective for inducing luminescence quenching by a reduction treatment at room temperature. A body color of the CaTiO3:Pr3+ sample was also changed from white to light yellow by the reduction due to the enhanced visible-light absorption. Such the dual luminescence/absorption switching was shown to be reversible with a subsequent oxidation and repeatable with a consecutive redox treatment.
引用
收藏
页码:694 / 701
页数:8
相关论文
共 24 条
[1]   UV-to-red relaxation pathways in CaTiO3:Pr3+ [J].
Boutinaud, P ;
Pinel, E ;
Dubois, M ;
Vink, AP ;
Mahiou, R .
JOURNAL OF LUMINESCENCE, 2005, 111 (1-2) :69-80
[2]   Ligand-Passivated Eu:Y2O3 Nanocrystals as a Phosphor for White Light Emitting Diodes [J].
Dai, Qilin ;
Foley, Megan E. ;
Breshike, Christopher J. ;
Lita, Adrian ;
Strouse, Geoffrey F. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (39) :15475-15486
[3]   Nanocrystalline CePO4:Tb as a novel oxygen sensing material on the basis of its redox responsive reversible luminescence [J].
Di, Weihua ;
Wang, Xiaojun ;
Ren, Xinguang .
NANOTECHNOLOGY, 2010, 21 (07)
[4]  
Diallo PT, 1997, PHYS STATUS SOLIDI A, V160, P255, DOI 10.1002/1521-396X(199703)160:1<255::AID-PSSA255>3.0.CO
[5]  
2-Y
[6]   New Synthesis Strategies for Luminescent YVO4:Eu and EuVO4 Nanoparticles with H2O2 Selective Sensing Properties [J].
Duee, Natacha ;
Ambard, Chrystel ;
Pereira, Franck ;
Portehault, David ;
Viana, Bruno ;
Valle, Karine ;
Autissier, Denis ;
Sanchez, Clement .
CHEMISTRY OF MATERIALS, 2015, 27 (15) :5198-5205
[7]   Preparation and optical characterization of Eu3+-doped CaTiO3 perovskite powders [J].
Duong Thi Mai Huong ;
Nguyen Hoang Nam ;
Le Van Vu ;
Nguyen Ngoc Long .
JOURNAL OF ALLOYS AND COMPOUNDS, 2012, 537 :54-59
[8]   Multivariable oxygen sensing based on photoluminescence and photoconductivity of TiO2 nanoparticles [J].
Eltermann, M. ;
Kiisk, V. ;
Kikas, A. ;
Lange, S. ;
Jaaniso, R. .
SENSORS AND ACTUATORS B-CHEMICAL, 2020, 303
[9]   Enhancement of long-lived luminescence in nanophosphors by surface defect passivation [J].
Fu, Linna ;
Wang, Jie ;
Chen, Na ;
Ma, Qinqin ;
Lu, Danqing ;
Yuan, Quan .
CHEMICAL COMMUNICATIONS, 2020, 56 (49) :6660-6663
[10]   CHARGE-TRANSFER SPECTRA OF TETRAVALENT LANTHANIDE IONS IN OXIDES [J].
HOEFDRAAD, HE .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1975, 37 (09) :1917-1921