Exciton, Biexciton, and Hot Exciton Dynamics in CsPbBr3 Colloidal Nanoplatelets

被引:81
作者
Vale, Brener R. C. [1 ,3 ]
Socie, Etienne [1 ]
Burgos-Caminal, Andres [1 ]
Bettini, Jefferson [2 ]
Schiavon, Marco A. [3 ]
Moser, Jacques-E. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Photochem Dynam Grp, CH-1015 Lausanne, Switzerland
[2] Univ Fed Sao Joao Del Rei, Dept Ciencias Nat, Grp Pesquisa Quim Mat, Campus Dom Bosco, BR-36301160 Sao Joao Del Rei, MG, Brazil
[3] Ctr Nacl Pesquisa Energia & Mat, Lab Nacl Nanotecnol, BR-13083970 Campinas, SP, Brazil
基金
瑞士国家科学基金会;
关键词
PEROVSKITE NANOCRYSTALS; AUGER RECOMBINATION; HALIDE PEROVSKITES; PHONON BOTTLENECK; BR; CSPBX3;
D O I
10.1021/acs.jpclett.9b03282
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lead halide perovskites have emerged as promising materials for light-emitting devices. Here, we report the preparation of colloidal CsPbBr3 nanoplatelets (3 x 4 x 23 nm(3)) experiencing a strong quasi-one-dimensional quantum confinement. Ultrafast transient absorption and broadband fluorescence up-conversion spectroscopies were employed to scrutinize the carrier and quasiparticle dynamics and to obtain a full description of the spectroscopic properties of the material. An exciton binding energy of 350 meV, an absorption cross section at 3.2 eV of 5.0 +/- 0.3 x 10(-15) cm(-2), an efficient biexciton Auger recombination lifetime of 9 +/- 1 ps, and a biexciton binding energy of 74 +/- 4 meV were determined. Moreover, a short-lived emission from hot excitons was observed, which is related to the formation of band-edge excitons. The time constant of both processes is 300 +/- 50 fs. These results show that CsPbBr3 nanoplatelets are indeed quite promising for light-emitting technological applications.
引用
收藏
页码:387 / 394
页数:15
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