Analysis of the low-temperature dielectric relaxation in CH3NH3PbI3 partially substituted with Sn and Ba

被引:0
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作者
Padchasri, Jintara [1 ,2 ]
Rujirawat, Saroj [1 ,2 ]
Yimnirun, Rattikorn [3 ,4 ]
Kolodiazhnyi, Taras [5 ]
机构
[1] Suranaree Univ Technol, Sch Phys, Inst Sci, Nakhon Ratchasima 30000, Thailand
[2] Suranaree Univ Technol, NANOTEC SUT COE Adv Funct Nanomat, Nakhon Ratchasima 30000, Thailand
[3] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Energy Sci & Engn, Wangchan 21210, Rayong, Thailand
[4] Vidyasirimedhi Inst Sci & Technol VISTEC, Res Network NANOTEC VISTEC Nanotechnol Energy, Wangchan 21210, Rayong, Thailand
[5] Natl Inst Mat Sci, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
来源
关键词
ORGANIC-INORGANIC PEROVSKITES; CHARGE-CARRIER MOBILITIES; LEAD HALIDE PEROVSKITES; SOLAR-CELLS; DYNAMICS; BR;
D O I
10.1007/s00339-018-2226-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this work, we partially replaced Pb with non-toxic elements to form hybrid perovskites CH 3 NH 3 Pb 0.9 M 0.1 I 3, where M = Sn 2+ and Ba 2+ and studied their dielectric properties. According to room-temperature Rietveld analysis, all compositions with 10 % substitution were tetragonal with a space group I4/ mcm. A notable dielectric relaxation was detected at T similar to 60-100 K, far below the orthorhombic-to-tetragonal phase transition at T similar to 155 K. To clarify the conflicting literature reports, the dielectric relaxation was fitted to both Arrhenius and Vogel-Fulcher models and showed no indication of the finite ( i. e. non-zero) dipolar freezing temperature. It is concluded, therefore, that the low-T dielectric dispersion is a signature of the Debye-type thermally activated re-orientation of the non-interacting electric dipoles with an activation energy of E a similar to 123 -171 meV.
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页数:7
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