Enhancing luminescence efficiency of CdSe quantum dots through the amine-assisted Z-type ligand

被引:1
作者
Huang, Xiaopeng [1 ]
Li, Nongsheng [1 ]
Kim, Keon-Han [2 ]
Chang, Qing [3 ]
Leng, Mengyu [1 ]
Wang, Junxin [4 ]
Cheng, Cheng [1 ]
Ao, Zhimin [5 ]
机构
[1] Beijing Normal Univ, Fac Arts & Sci, Dept Chem, Zhuhai 519087, Peoples R China
[2] Lawrence Berkeley Natl Lab, Chem Sci Div, 1 Cyclotron Rd, Berkeley, CA 94720 USA
[3] Beijing Normal Univ, Expt Teaching Platform, Zhuhai 519087, Peoples R China
[4] Univ Cambridge, Dept Mat Sci & Met, 27 Charles Babbage Rd, Cambridge CB3 0FS, England
[5] Beijing Normal Univ, Adv Interdisciplinary Inst Environm & Ecol, Guangdong Prov Key Lab Wastewater Informat Anal &, Zhuhai 519087, Peoples R China
基金
欧盟地平线“2020”; 中国国家自然科学基金;
关键词
CORE/SHELL NANOCRYSTALS; CARBOXYLATE; SURFACE; CDTE; ABSORPTION; GROWTH;
D O I
10.1016/j.xcrp.2024.102268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic ligands play a key role in passivating quantum dots (QDs), facilitating their green production and large-scale synthesis. Alkyl- amines, in particular, significantly enhance the photoluminescence efficiency of CdSe QDs. However, the interaction mechanism between alkylamines and QDs remains unclear. In this study, we propose a mode of interaction between amines and QDs, referred to as Z* ligands, which are formed by the combination of alkylamines with Z-type cadmium carboxylate. Our findings demonstrate that, compared to traditional Z-type, L-type, and X-type ligands, the Z* ligand exhibits more pronounced fluorescence enhancement of QDs while minimizing the surface etching effect. Through density functional theory calculations, we further elucidate the mechanism by which the Z* ligand enhances the photoluminescence efficiency and stabilizes the QD surface. These insights deepen our understanding of organic ligand passivation on QDs and open new paths for the green synthesis of highly luminescent QDs.
引用
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页数:19
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