钝化
光致发光
材料科学
钙钛矿(结构)
量子点
超晶格
卤化物
兴奋剂
氯
紫外线
锶
光电子学
纳米技术
化学工程
无机化学
化学
图层(电子)
冶金
有机化学
工程类
作者
Yongqiang Ji,Minqiang Wang,Zhi Yang,Hao Wang,Muhammad Amin Padhiar,Hengwei Qiu,Jialin Dang,Yinru Miao,Yun Zhou,Arshad Saleem Bhatti
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2022-01-01
卷期号:14 (6): 2359-2366
被引量:26
摘要
Among the lead halide perovskites, the photoluminescence quantum yields (PLQYs) of perovskite quantum dots (PQDs) in the violet region are the very lowest. This is an obstacle to the optical applications across the entire visible area based on perovskite materials. Herein, we report a novel strontium (Sr)-substitution along with chlorine passivation strategy to enhance the PLQYs of CsPbCl3 PQDs. We surprisingly found that when the molar ratio of Sr2+/Pb2+ = 0.1/0.9, CsSr0.1Pb0.9Cl3 PQDs exhibit strong single-color violet emission, which is attributed to the effective passivation of chlorine defects. We further found spontaneous self-assembly of PQDs into highly emissive PSCs from the precursor in a highly concentrated solution. Moreover, by dilution of these PSCs, a few small PQD aggregates can be regained, which is similar to the PQDs formed at lower concentrations. Benefiting from the superior collective properties of individual PQDs, these highly fluorescent CsSr0.1Pb0.9Cl3 PSCs can maintain good stability even when directly immersed in water or exposed to illumination.
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