Synthesis and characterization of a CsPbCl3 perovskite doped with Nd3+: structural, optical, and energy transfer properties

被引:1
作者
Stefanski, Mariusz [1 ]
Bondzior, Bartosz [1 ]
Basinski, Adam [1 ]
Ptak, Maciej [1 ]
Lou, Bibo [2 ,3 ]
Ma, Chong-Geng [2 ,3 ]
机构
[1] Polish Acad Sci, Inst Low Temp & Struct Res, PL-50422 Wroclaw, Poland
[2] Chongqing Univ Posts & Telecommun, Sch Optoelect Engn, 2 Chongwen Rd, Chongqing 400065, Peoples R China
[3] Chongqing Univ Posts & Telecommun, CQUPT BUL Innovat Inst, 2 Chongwen Rd, Chongqing 400065, Peoples R China
基金
中国国家自然科学基金;
关键词
LANTHANIDE; LUMINESCENCE; PHOTOLUMINESCENCE; EMISSION;
D O I
10.1039/d4qi00171k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The purpose of this paper is to synthesize a micrometric inorganic perovskite CsPbCl3:Nd3+ and investigate the impact of doping with rare-earth ions on structural and optical properties, as well as energy transfer pathways between the host and dopant. Herein, we report the solid-state reaction synthesis of a concentration series of CsPbCl3:x%Nd3+ annealed under a nitrogen atmosphere. Additional doping of a material that already exhibits luminescence with an optically active ion increases its application potential. Structural features were determined using X-ray powder diffraction and Raman spectroscopy. Morphology studies performed with scanning electron microscopy revealed micrometric, well-separated cubic-like crystallites with a good distribution of individual elements. Surprisingly, a photoluminescence (PL) study showed that only blue emission appears when the material is excited with a diode operating in the UV range. Apparently, the emission of Nd3+ ions can only be obtained with direct excitation of the lanthanide. The photoluminescence excitation (PLE) spectrum monitored for Nd3+ emission confirmed the lack of energy transfer between the host and dopant. Possible explanations for this behavior have been put forth and substantiated by the first-principles electronic structure calculations in the framework of hybrid density functional theory.
引用
收藏
页码:2626 / 2633
页数:8
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