材料科学
纳米晶
纳米材料
钝化
模板
纳米技术
微流控
同种类的
钙钛矿(结构)
化学工程
图层(电子)
工程类
物理
热力学
作者
Jun‐Hyung Im,Myeonggeun Han,Jisu Hong,Hye-In Kim,Kwang-Suk Oh,Taesu Choi,Abd. Rashid bin Mohd Yusoff,Maria Vasilopoulou,Eunsook Lee,Chan‐Cuk Hwang,Yong‐Young Noh,Young‐Ki Kim
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-02
标识
DOI:10.1021/acsnano.4c13217
摘要
Perovskite nanocrystals (PNCs) are promising active materials because of their outstanding optoelectronic properties, which are finely tunable via size and shape. However, previous synthetic methods such as hot-injection and ligand-assisted reprecipitation require a high synthesis temperature or provide limited access to homogeneous PNCs, leading to the present lack of commercial value and real-world applications of PNCs. Here, we report a room-temperature approach to synthesize PNCs within a liquid crystalline antisolvent, enabling access to PNCs with a precisely defined size and shape and with reduced surface defects. We demonstrate that elastic strains and long-range molecular ordering of the liquid crystals play a key role in not only regulating the growth of PNCs but also promoting high surface passivation of PNCs with ligands. The approach is a simple, rapid, and room-temperature process, yet it enables access to highly homogeneous PNCs on a mass scale with substantially reduced surface defect states leading to significantly enhanced optoelectronic features. Our results provide a versatile and generalizable strategy to be broadly compatible with a range of nanomaterials and other synthetic methods such as ligand exchange and microfluidic processes.
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