Unconventional route to dual-shelled organolead halide perovskite nanocrystals with controlled dimensions, surface chemistry, and stabilities

被引:129
作者
He, Yanjie [1 ]
Yoon, Young Jun [1 ]
Harn, Yeu Wei [1 ]
Biesold-McGee, Gill V. [1 ]
Liang, Shuang [1 ]
Lin, Chun Hao [1 ]
Tsukruk, Vladimir V. [1 ]
Thadhani, Naresh [1 ]
Kang, Zhitao [1 ,2 ]
Lin, Zhiqun [1 ]
机构
[1] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[2] Georgia Tech Res Inst, Electroopt Syst Lab, Atlanta, GA 30332 USA
来源
SCIENCE ADVANCES | 2019年 / 5卷 / 11期
基金
美国国家科学基金会;
关键词
CESIUM LEAD HALIDE; HIGHLY LUMINESCENT; QUANTUM DOTS; CH3NH3PBBR3; PEROVSKITE; COLLOIDAL SYNTHESIS; OPPORTUNITIES; CSPBX3; BR; CL;
D O I
10.1126/sciadv.aax4424
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The past few years have witnessed rapid advances in the synthesis of high-quality perovskite nanocrystals (PNCs). However, despite the impressive developments, the stability of PNCs remains a substantial challenge. The ability to reliably improve stability of PNCs while retaining their individual nanometer size represents a critical step that underpins future advances in optoelectronic applications. Here, we report an unconventional strategy for crafting dual-shelled PNCs (i.e., polymer-ligated perovskite/SiO2 core/shell NCs) with exquisite control over dimensions, surface chemistry, and stabilities. In stark contrast to conventional methods, our strategy relies on capitalizing on judiciously designed star-like copolymers as nanoreactors to render the growth of core/shell NCs with controlled yet tunable perovskite core diameter, SiO2 shell thickness, and surface chemistry. Consequently, the resulting polymer-tethered perovskite/SiO2 core/shell NCs display concurrently a stellar set of substantially improved stabilities (i.e., colloidal stability, chemical composition stability, photostability, water stability), while having appealing solution processability, which are unattainable by conventional methods.
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页数:11
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