摘要
采用柠檬酸凝胶-燃烧法合成了CaLa1-xAl3O7∶xEu3+(0.05≤x≤0.8)材料的前驱粉末,在低于700℃退火处理时,得到非晶态样品,而高于800℃退火处理后为纯相的CaLa1-xAl3O7∶xEu3+粉末样品。通过激发光谱和发射光谱研究了Eu3+在CaLaAl3O7基质中的发光性能及Eu3+掺杂量,退火温度和柠檬酸与金属离子的配比等对发光强度的影响。结果显示,非晶态和晶态CaLa1-xAl3O7∶xEu3+样品均可发光,非晶态样品的最强激发峰出现在7F0—5D2的465 nm处,而晶相样品的最强激发峰为7F0—5L6跃迁的394nm。非晶态粉末在465 nm激发下发射光谱由5D0—7F0的578 nm和5D0—7F1的587 nm及5D0—7F2的615nm组成。而晶态粉末在394 nm激发下的发射光谱与非晶态相比5D0—7F0跃迁消失了,同时5D0—7F1跃迁发生谱线劈裂,出现在587和596 nm两处。随着退火温度的升高,主峰615 nm强度增强了,但5D0—7F1跃迁峰的增强更加明显。
Using the gel-combustion method the precursors of CaLa1-xAl3O7∶xEu^3+(0.05≤x≤0.8) were prepared.When annealing temperature was below 700 ℃,the materials were in amorphous state,while as annealing temperature was above 800 ℃,the high purity CaLa1-xAl3O7∶xEu^3+ crystalline materials were obtained.The luminescence properties of CaLa1-xAl3O7∶xEu^3+ both in amorphous and crystalline phases were investigated,and the results of excitation spectrum show a similar charge transition band of Eu^3+-O^2-between 230 nm and 320 nm and a series of f-f transition of Eu^3+ ion.However,the strongest band of amorphous material was at 465 nm corresponding to ^7F0-^5D2 transition,and those of the crystalline materials were at 394 nm corresponding to ^7F0-^5L6 transition of Eu^3+ ion.In amorphous state materials the emission intensity of excitation wavelength 465 nm was stronger than that of 394 nm,and composition of ^5D0-^7F0 transition at 578 nm,^5D0-^7F1 transition at 587 nm and ^5D0-^7F2 transition at 615 nm.In crystalline material,the emission intensity of excitation wavelength of 394 nm was stronger than that of 465 nm,the ^5D0-^7F0 transition disappeared,and the ^5D0-^7F1 transition split into 587 nm and 596 nm.With the increase in temperature,the strongest band at 615 nm increased,and what is more,the ^5D0-^7F1 transition increased remarkably.In CaLa1-xAl3O7∶xEu^3+,when x=0.2 for the co-doping Eu^3+ ion and the mol proportion of citric acid and metal ion(C/M) was 1.2,the luminescence intensity was the highest.
出处
《光谱学与光谱分析》
SCIE
EI
CAS
CSCD
北大核心
2008年第12期2781-2784,共4页
Spectroscopy and Spectral Analysis
基金
国家自然科学基金项目(20161001)
内蒙古自然科学基金项目(200711020213)资助