配体(生物化学)
纳米晶
聚苯乙烯
聚合物
钙钛矿(结构)
材料科学
量子点
离子键合
光化学
化学
化学工程
结晶学
纳米技术
离子
有机化学
工程类
受体
生物化学
作者
Xiao Liu,Jing Lv,Shunwei Yao,Yanan Wang,Peng Lin,Jing Chen,Xiaolin Liu,Jia Lin,Xianfeng Chen
标识
DOI:10.1002/chem.202203971
摘要
Perovskite nanocrystals (NCs) exhibit attractive photophysical properties by combining the excellent optoelectronic properties of bulk perovskites with the strong quantum confinement effect at the nanoscale. However, CsPbI3 NCs easily transform into a non-perovskite phase because of the ionic lattice and dynamic ligand binding. Herein, stable black-phase CsPbI3 NCs capped with a new organic ligand, HO-PS-N3 (HOPS), which consists of a polystyrene segment with hydroxyl and azide end groups, are reported. This organic polymer ligand passivated the surface defects and enhanced the stability of CsPbI3 NCs by exposing the linking hydrophobic polystyrene segment. Consequently, the optimized CsPbI3 NCs exhibit significantly improved resistance to moisture or light and maintained 70 % of the original luminous intensity after immersion in water for two months. The theoretical results revealed that the binding energy of the HOPS ligand on the surface of the CsPbI3 NCs is higher than that of the commonly used oleic acid, alleviating the defects-induced degradation during purification. Thus, surface-stabilized CsPbI3 NCs are beneficial for a broad range of optoelectronic applications.
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