Composition-dependent emission linewidth broadening in lead bromide perovskite (APbBr3, A = Cs and CH3NH3) nanoparticles

被引:13
作者
Ham, Sujin [1 ,2 ]
Chung, Heejae [1 ,2 ]
Kim, Tae-Woo [1 ,2 ]
Kim, Jiwon [3 ,4 ]
Kim, Dongho [1 ,2 ]
机构
[1] Yonsei Univ, Spect Lab Funct Elect Syst, 50 Yonsei Ro, Seoul 03722, South Korea
[2] Yonsei Univ, Dept Chem, 50 Yonsei Ro, Seoul 03722, South Korea
[3] Yonsei Univ, Sch Integrated Technol, 85 Songdogwahak Ro, Incheon 21983, South Korea
[4] Yonsei Univ, Underwood Int Coll, 85 Songdogwahak Ro, Incheon 21983, South Korea
基金
新加坡国家研究基金会;
关键词
LIGHT-EMITTING-DIODES; NANOCRYSTALLITE QUANTUM DOTS; SINGLE-PHOTON EMISSION; HALIDE PEROVSKITES; SPECTRAL DIFFUSION; ROOM-TEMPERATURE; FLUORESCENCE INTERMITTENCY; BLINKING; PHOTOLUMINESCENCE; CSPBX3;
D O I
10.1039/c7nr07330e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lead halide perovskite nanoparticles (NPs) are attractive as they exhibit excellent color purity and have a tunable band gap, and can thus be applied in highly efficient photovoltaic and light-emitting diodes. Fundamental studies of emission linewidth broadening due to spectral shifts in perovskite NPs may suggest a way to improve their color purity. However, the carrier-induced Stark shift that causes spectral diffusion still requires investigation. In this study, we explore composition-related emission linewidth broadening by comparing CsPbBr3 and CH3NH3PbBr3 (MAPbBr(3)) perovskite NPs. We find that the MAPbBr(3) NPs are more sensitive to fluctuations in the local electric fields than the CsPbBr3 NPs due to an intrinsic difference in the dipole moment between the two A cations (Cs and MA), which shows a carrier-induced Stark shift. The results indicate that the compositions of perovskite NPs are closely associated with emission linewidth broadening and they also provide insights into the development of NP-based devices with high color purity.
引用
收藏
页码:2207 / 2212
页数:6
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