Electrospinning preparation and photoluminescence properties of Y3Al5O12:Ce3+, Tb3+ nanobelts

被引:2
作者
Bi, Fei [1 ]
Gai, Guangqing [1 ]
Dong, Xiangting [2 ]
Xiao, Shanshan [1 ]
Wang, Jinxian [2 ]
Liu, Guixia [2 ]
Zhao, Li [1 ]
Wang, Liyan [1 ]
机构
[1] Jilin Jianzhu Univ, Coll Mat Sci & Engn, Lab Bldg Energy Saving Technol Engn, Changchun 130118, Peoples R China
[2] Changchun Univ Sci & Technol, Key Lab Appl Chem & Nanotechnol Univ Jilin Prov, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
COAXIAL NANOFIBERS; FABRICATION; PERFORMANCE; EMISSION;
D O I
10.1007/s10854-016-6084-y
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Novel nanostructure of Y3Al5O12:Ce3+, Tb3+ (denoted as YAG:Ce3+, Tb3+ for short) nanobelts and nanofibers were fabricated by calcination of the respective electrospun PVP/[Y(NO3)(3) + Ce(NO3)(3) + Tb(NO3)(3) + Al(NO3)(3)] composite nanobelts. YAG:Ce3+, Tb3+ nanobelts are cubic in structure with space group of I(a)3d. The thickness and width of the YAG:Ce3+, Tb3+ nanobelts are respectively 118 nm and 4.09 +/- 0.41 mu m. The excitation spectra detected of 520 nm for Ce3+ emission represented 4f (8) -> 4f (7)5d transition band at 273 nm by Tb3+ and other two bands by Ce3+. When excited with a UV light of 273 nm, YAG:Ce3+, Tb3+ nanobelts showed the characteristic Tb3+ peaks, as well as Ce3+ emission peak. The results concluded that the energy transfer pathway in YAG:Ce3+, Tb3+ nanobelts system was one-way from Tb3+ to Ce3+. Commission International del'Eclairage chromaticity coordinates indicated that the emission colors of YAG:Ce3+, Tb3+ nanobelts were tunable by changing the concentration of doping Ce3+, which could be applied in the field of optical telecommunication and optoelectronic devices. The possible formation mechanism of YAG:Ce3+, Tb3+ nanobelts was also proposed.
引用
收藏
页码:4498 / 4505
页数:8
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