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Size Dependence of Trion and Biexciton Binding Energies in Lead Halide Perovskite Nanocrystals
被引:8
|作者:
Cho, Kenichi
[1
]
Sato, Takao
[2
]
Yamada, Takumi
[1
]
Sato, Ryota
[1
]
Saruyama, Masaki
[1
]
Teranishi, Toshiharu
[1
]
Suzuura, Hidekatsu
[2
]
Kanemitsu, Yoshihiko
[1
]
机构:
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[2] Hokkaido Univ, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
来源:
关键词:
perovskite nanocrystals;
single dot spectroscopy;
trion;
biexciton;
binding energies;
OPTICAL-PROPERTIES;
ANION-EXCHANGE;
QUANTUM DOTS;
LUMINESCENCE;
CONFINEMENT;
EMISSION;
EXCITONS;
CSPBX3;
MASSES;
STATES;
D O I:
10.1021/acsnano.3c11842
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Lead halide perovskite nanocrystals (NCs) have attracted much attention as light-source materials for light-emitting diodes, lasers, and quantum light emitters. The luminescence properties of perovskite NCs and the performance of NC-based light-source devices depend on trion and biexciton dynamics. Here, we examined the size dependence of trion and biexciton binding energies by conducting low-temperature single-dot spectroscopy on three different perovskite NCs: CsPbBr3, CsPbI3, and FAPbBr(3). While the photoluminescence spectral widths of the all-inorganic CsPbBr3 and CsPbI3 NCs were narrow, compared with those of the organic-inorganic hybrid FAPbBr(3) NCs, the binding energies of trions and biexcitons of all three samples showed similar size dependences, independent of the A-site cation and halogen. The effective-mass approximation calculations implied the importance of dynamical dielectric screening on the formation of trions and biexcitons.
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页码:5723 / 5729
页数:7
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