Controlling Electronic-Ionic Kinetics via Size Engineering in CsPbBr3 Perovskite Nanocrystals

被引:0
|
作者
Kumar, Ramesh [1 ]
Beniwal, Shivang [2 ,3 ]
Suhail, Atif [3 ]
Rakheja, Bhavya [1 ]
Bag, Monojit [3 ]
Johansson, Erik M. J. [1 ]
机构
[1] Uppsala Univ, Dept Chem, Angstrom Lab, SE-E75120 Uppsala, Sweden
[2] Univ Liverpool, Mat Innovat Factory, Liverpool L7 3NY, England
[3] Indian Inst Technol Roorkee, Adv Res Electrochem Impedance Spect Lab, Roorkee 247667, India
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 33期
关键词
CONDUCTIVITY;
D O I
10.1021/acs.jpcc.4c02991
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
Owing to the exceptional photovoltaic and optoelectronic properties of metal halide perovskites, they have sparked an intensive interest in the research community. CsPbBr3 perovskite nanocrystals (NCs) have come into sight due to their versatile properties that can be achieved through structural modification. While the prior research on perovskite nanocrystals has focused mainly on tuning optical and electronic properties, the understanding of their electronic-ionic kinetics still remains a significant research gap. In this work, we explore how the size of CsPbBr3 NCs impacts their electronic-ionic properties by using electrochemical impedance spectroscopy (EIS). We systematically tune NC size and investigate the resulting dielectric properties, conductivity, and capacitance. Notably, larger NCs exhibit anomalous behavior similar to that of perovskite polycrystalline thin films in the range of 0.4-0.6 V, indicating strong electronic-ionic coupling. Conversely, smaller NCs display weak electronic-ionic coupling due to ion localization. Additionally, this study sheds light on the electronic-ionic behavior of NCs approaching quantum confinement with a size reduction, suggesting opportunities for defect engineering. Ultimately, this work will pave the way for developing advanced electronic devices utilizing perovskite nanocrystals.
引用
收藏
页码:13917 / 13925
页数:9
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