Strong violet emission from ultra-stable strontium-doped CsPbCl3 superlattices

被引:21
作者
Ji, Yongqiang [1 ,2 ]
Wang, Minqiang [1 ]
Yang, Zhi [1 ]
Wang, Hao [1 ]
Padhiar, Muhammad Amin [1 ]
Qiu, Hengwei [3 ]
Dang, Jialin [1 ]
Miao, Yinru [1 ]
Zhou, Yun [1 ]
Bhatti, Arshad Saleem [4 ]
机构
[1] Xi An Jiao Tong Univ, Int Ctr Dielect Res ICDR, Key Lab,Educ Minist,Shaanxi Engn Res Ctr Adv Ener, Sch Elect & Informat Engn,Elect Mat Res Lab EMIZL, Xian 710049, Peoples R China
[2] Peking Univ, Sch Phys, State Key Lab Artificial Microstruct & Mesoscop P, Beijing 100871, Peoples R China
[3] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[4] COMSATS Inst Informat Technol, Ctr Micro & Nano Devices, Dept Phys, Islamabad 44500, Pakistan
基金
国家重点研发计划; 中国博士后科学基金; 中国国家自然科学基金;
关键词
PEROVSKITE QUANTUM DOTS; HIGHLY LUMINESCENT; NANOCRYSTALS; PHOTOLUMINESCENCE;
D O I
10.1039/d1nr07848h
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:2359 / 2366
页数:8
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