钙钛矿(结构)
量子点
材料科学
硫化铅
铅(地质)
配体(生物化学)
硫化物
接口(物质)
理论(学习稳定性)
化学工程
图层(电子)
纳米技术
化学
复合材料
计算机科学
冶金
工程类
受体
毛细管数
地貌学
生物化学
机器学习
毛细管作用
地质学
作者
Ruiman Ma,Zhenwei Ren,Can Li,Yong Wang,Zhanfeng Huang,Yong Zhao,Tingbin Yang,Yongye Liang,Xiao Wei Sun,Wallace C. H. Choy
出处
期刊:Small
[Wiley]
日期:2020-09-22
卷期号:16 (41)
被引量:24
标识
DOI:10.1002/smll.202002628
摘要
Abstract While organic–inorganic halide perovskite solar cells (PSCs) show great potential for realizing low‐cost and easily fabricated photovoltaics, the unexpected defects and long‐term stability against moisture are the main issues hindering their practical applications. Herein, a strategy is demonstrated to address the main issues by introducing lead sulfide quantum dots (QDs) on the perovskite surface as the multifunctional interface layer on perovskite film through establishing perovskite as the ligand on PbS QDs. Meanwhile, the multifunctions are featured in three aspects including the strong interactions of PbS QDs with perovskites particularly at the grain boundaries favoring good QDs coverage on perovskites for ultimate smooth morphology; an inhibition of iodide ions mobilization by the strong interaction between iodide and the incorporated QDs; and the reduction of the dangling bonds of Pb 2+ by the sulfur atoms of PbS QDs. Finally, the device performances are highly improved due to the reduced defects and non‐radiative recombination. The results show that both open‐circuit voltage and fill factor are significantly improved to the high values of 1.13 V and 80%, respectively in CH 3 NH 3 PbI 3 ‐based PSCs, offering a high efficiency of 20.64%. The QDs incorporation also enhances PSCs’ stability benefitting from the induced hydrophobic surface and suppressed iodide mobilization.
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