Highly efficient A-site cation exchange in perovskite quantum dot for solar cells

被引:8
|
作者
Zhao, Chenyu [1 ]
Zhang, Xuliang [1 ]
Huang, Hehe [1 ]
Yuan, Jianyu [1 ,2 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, 199 Renai Rd, Suzhou 215123, Jiangsu, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Adv Negat Carbon Technol, Suzhou 215123, Jiangsu, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2022年 / 157卷 / 03期
基金
中国国家自然科学基金;
关键词
ALPHA-CSPBI3; PEROVSKITE; HALIDE PEROVSKITES; FORMAMIDINIUM; NANOCRYSTALS; STABILITY; CSPBX3;
D O I
10.1063/5.0100258
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
The mixed cation colloidal Cs(1-X)FA(X)PbI(3) perovskite quantum dots (PQDs) obtained by cation exchange between CsPbI3 and FAPbI(3) PQDs have been reported to exhibit enhanced photovoltaic performance. However, the cation exchange mechanism requires further in-depth investigation in terms of both material properties and device application. In this work, the impact of PQD weight ratio, PQD concentration, and host solvent polarity during cation exchange is comprehensively investigated for the first time. In addition, the whole exchange process under varying conditions is monitored by photoluminescence spectroscopy. As a result, we observe extremely fast cation exchange (& SIM;20 min) under a condition at a CsPbI3/FAPbI(3) PQD weight ratio of 1:1, a concentration of 70 mg/ml, and a host solvent using toluene. Moreover, we directly fabricate a PQD solar cell device using these obtained mixed cation Cs(0.5)FA(0.5)PbI(3) PQDs and achieved an enhanced power conversion efficiency of 14.58%. We believe that these results would provide more insights into the cation exchange in emerging PQDs toward efficient photovoltaic fabrication and application. Published under an exclusive license by AIP Publishing.
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页数:7
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