量子点
钙钛矿(结构)
材料科学
钝化
纳米技术
电导率
成核
基质(化学分析)
纳米尺度
光电子学
化学
结晶学
物理化学
复合材料
有机化学
图层(电子)
作者
Yao Shi,Yuan Lin,Zeke Liu,Yuan Lu,Biao Yuan,Wan‐Shan Shen,Bingyan Xue,Yannan Zhang,Yuli Qian,Fangchao Li,Xuliang Zhang,Yang Liu,Yao Wang,Lu Wang,Jianyu Yuan,Liang‐Sheng Liao,Boping Yang,Yi Yu,Wanli Ma
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-07-15
卷期号:16 (7): 10534-10544
被引量:32
标识
DOI:10.1021/acsnano.2c01791
摘要
Their nanoscale size endows perovskite quantum dots (QDs) with processing flexibility and high tunability of optoelectronic properties. The vast surface area also provides an opportunity for ligand engineering to offer QDs extra protection, which however, will impede charge transport in the QD array. Currently, the surface treatments that can balance both stability and conductivity of the perovskite QD array remain a huge challenge. Here, we report in situ growth of an atomic guanidinium lead iodide perovskite matrix on CsPbI3 QDs. In addition to the effect of trap passivation, the matrix can also provide substantial surface strain to improve the QD phase stability. Meanwhile, the ultrathin matrix allows efficient coupling and charge transport in the QD solids. As a result, the CsPbI3 QD solar cells can achieve both superior device stability and performance. We believe the development of a multifunctional surface matrix will become one of the future research focuses in perovskite QD-based devices.
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