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Enhanced Stability and Tunable Photoluminescence in Perovskite CsPbX3/ZnS Quantum Dot Heterostructure
被引:156
|作者:
Chen, Weiwei
[1
]
Hao, Jiongyue
[1
]
Hu, Wei
[1
]
Zang, Zhigang
[1
]
Tang, Xiaosheng
[1
]
Fang, Liang
[2
]
Niu, Tianchao
[3
]
Zhou, Miao
[1
]
机构:
[1] Chongqing Univ, Coll Optoelet Engn, Minist Educ, Key Lab Optoelect Technol & Syst, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Coll Phys, Dept Appl Phys, Chongqing 401331, Peoples R China
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
来源:
基金:
中国国家自然科学基金;
关键词:
all-inorganic perovskites;
first principles;
heterojunction;
optical excitation;
quantum dots;
LIGHT-EMITTING-DIODES;
OPTICAL-PROPERTIES;
NANOCRYSTALS;
PERFORMANCE;
BR;
CL;
EMISSION;
D O I:
10.1002/smll.201604085
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
All-inorganic perovskite CsPbX3 (X = Cl, Br, I) and related materials are promising candidates for potential solar cells, light emitting diodes, and photodetectors. Here, a novel architecture made of CsPbX3/ZnS quantum dot heterodimers synthesized via a facile solution-phase process is reported. Microscopic measurements show that CsPbX3/ZnS heterodimer has high crystalline quality with enhanced chemical stability, as also evidenced by systematic density functional theory based first-principles calculations. Remarkably, depending on the interface structure, ZnS induces either n-type or p-type doping in CsPbX3 and both type-I and type-II heterojunctions can be achieved, leading to rich electronic properties. Photoluminescence measurement results show a strong blue-shift and decrease of recombination lifetime with increasing sulfurization, which is beneficial for charge diffusion in solar cells and photovoltaic applications. These findings are expected to shed light on further understanding and design of novel perovskite heterostructures for stable, tunable optoelectronic devices.
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页数:8
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