光致发光
材料科学
微晶
荧光粉
发光
分析化学(期刊)
兴奋剂
纳米颗粒
吸收(声学)
吸收光谱法
纳米技术
化学
光电子学
光学
色谱法
物理
复合材料
冶金
作者
L. Lamiri,B. Kahouadji,Mourad Berd,Abdelmoumen Abdellatif,Lotfi Benchallal,L. Guerbous,Salim Ouhenia,Abdelhafid Souici,Leila Amiour,Abdelhalim Zoukel,M. Samah
标识
DOI:10.1016/j.jre.2022.03.006
摘要
Nanosized 1 at% Sm3+ doped Y2O3 powders were prepared by an ultrasound assisted sol-gel method. Y2O3:Sm3+ powders crystallize in Y2O3 pure cubic phase and XRD analysis shows that the as-used agitation protocol affects strongly the crystallite's shape and mean size. The recorded emission spectra under λem=600nm exhibit two absorption bands; the first one is assigned to O2− → Sm3+ charge transfer state (CTS) with a maximum absorption at 223 nm, and the second is due to intra-configurational transition 4f5-4f5 of Sm3+ with a maximum absorption at 407 nm. The 223 and 407 nm transitions are attributed to characteristics intra-configurational transitions of Sm3+. All emission spectra are dominated by reddish/orange luminescence located at 606 nm and assigned to 4G5/2 → 6H7/2 transition. It is found that the photoluminescence intensity of samples obtained under excitation at 407 nm is 60 times smaller than that obtained under 223 nm excitation. Decay time measurements of the 4G5/2 → 6H7/2 luminescence transition indicate that decay time of nano-sized powder is significantly shorter than bulk material one.
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