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)
热力学
物理
工程类
作者
Jun‐Hyung Im,Myeonggeun Han,Jisu Hong,Hyein 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
卷期号:19 (1): 1177-1189
被引量:6
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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