Unconventional route to dual-shelled organolead halide perovskite nanocrystals with controlled dimensions, surface chemistry, and stabilities
Author(s) -
Yanjie He,
Young Jun Yoon,
Yeu Wei Harn,
Gill V. BiesoldMcGee,
Shuang Liang,
Chun Lin,
Vladimir V. Tsukruk,
Naresh Thadhani,
Zhitao Kang,
Zhiqun Lin
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aax4424
Subject(s) - halide , nanocrystal , perovskite (structure) , nanotechnology , dual (grammatical number) , chemistry , chemical engineering , materials science , inorganic chemistry , crystallography , art , literature , engineering
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/SiO 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, SiO shell thickness, and surface chemistry. Consequently, the resulting polymer-tethered perovskite/SiO 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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