Zero-Dimensional (Piperidinium)2MnBr4: Ring Puckering-Induced Isostructural Transition and Strong Electron-Phonon Coupling- Mediated Self-Trapped Exciton Emission

被引:13
|
作者
Panda, Debendra Prasad [1 ,2 ]
Swain, Diptikanta [3 ]
Sundaresan, A. [1 ,2 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, Sch Adv Mat, Bangalore 560064, India
[2] Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, Bangalore 560064, India
[3] Inst Chem Technol, IndianOil Odisha Campus, Bhubaneswar 751013, India
关键词
HYBRID METAL HALIDE; LIGHT EMISSION; PEROVSKITE; PHOTOLUMINESCENCE; DYNAMICS; TEMPERATURE;
D O I
10.1021/acs.inorgchem.2c01601
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We report on the synthesis, structure, and photo physical properties of a lead-free organic-inorganic hybrid halide, (Piperidinium)(2)MnBr4 (PipMBr). It crystallizes in a monoclinic P2(1)/n structure, with isolated MnBr4 tetrahedra representing a zero dimensional compound. It undergoes a reversible isostructural transition at 422/417 K in the heating/cooling cycle owing to the hydrogen-bonding rearrangement mediated by ring puckering of piperidinium cations. This compound exhibits green emission with a photoluminescence quantum yield of 51%. Interestingly, strong electron-longitudinal optical phonon coupling with gamma LO of 237 meV is evidenced from the broadening of the temperature-dependent emission linewidth and the Raman spectrum. Such strong electron-phonon coupling and a relatively low Debye temperature (137 K) suggest the self-trapped exciton emission in this compound.
引用
收藏
页码:11377 / 11386
页数:10
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