Structural,morphological and photoluminescence characterizations of Sm^(3+) doped Y_(2)O_(3) nano-sized phosphors synthesized by ultrasound assisted sol-gel method
Structural,morphological and photoluminescence characterizations of Sm3+ doped Y2O3 nano-sized phosphors synthesized by ultrasound assisted sol-gel method作者机构:Department of TCSNUniversity of BejaiaBejaia06000Algeria Department of TechnologyUniversity of BejaiaBejaia06000Algeria Department of TechnologyLaboratory of LECVEUniversity of BejaiaBejaiaO6000Algeria Department of Physics of MaterialsUniversity of Science and Technology Houari BoumedieneAlgiersAlgeria Laser Department/Nuclear Research Center of Algiers(CRNA)02Boulevard Frantz FanonB.P.399Algiers16000Algeria Laboratory of Physical-chemistryUniversity of BejaiaBejaia06000Algeria Phase Transformation LaboratoryUniversite Freres Mentouri Constantine 1Algeria Laboratory Physico-Chemistry of MaterialsLaghouat UniversityTechnical Platform of Physico-Chemical Analysis(PTAPC-Laghouat-CRAPC)LaghouatAlgeria
出 版 物:《Journal of Rare Earths》 (稀土学报(英文版))
年 卷 期:2023年第41卷第1期
页 面:51-59页
核心收录:
学科分类:081702[工学-化学工艺] 08[工学] 0817[工学-化学工程与技术] 1010[医学-医学技术(可授医学、理学学位)] 0703[理学-化学] 0702[理学-物理学] 1009[医学-特种医学]
基 金:supported by Nuclear Research Center of Algiers(CRNA) Department of Laser Luminescence Laboratory
主 题:Y_(2)O_(3):Sm^(3+)nano-sized powder Sol-gel method Ultrasound Charge transfer Photoluminescence Rare earths
摘 要:Nanosized 1 at% Sm^(3+)doped Y_(2)O_(3)powders were prepared by an ultrasound assisted sol-gel method.Y_(2)O_(3):Sm^(3+)powders crystallize in Y_(2)O_(3)pure cubic phase and XRD analysis shows that the as-used agitation protocol affects strongly the crystallite’s shape and mean *** recorded emission spectra under λ_(em)=600 nm exhibit two absorption bands;the first one is assigned to O^(2-)→Sm^(3+)charge transfer state(CTS) with a maximum absorption at 223 nm,and the second is due to intraconfigurational transition 4f^(5)-4f^(5) of Sm^(3+) with a maximum absorption at 407 *** 223 and 407 nm transitions are attributed to characteristics intra-configurational transitions of Sm^(3+).All emission spectra are dominated by reddish/orange luminescence located at 606 nm and assigned to ^(4)G_(5/2)→^(6)H_(7/2) *** is found that the photoluminescence intensity of samples obtained under excitation at 407 nm is 60 times smaller than that obtained under 223 nm *** time measurements of the ^(4)G_(5/2)→^(6)H_(7/2) luminescence transition indicate that decay time of nano-sized powder is significantly shorter than bulk material one.