Organolead Halide Perovskite Nanocrystals: Branched Capping Ligands Control Crystal Size and Stability

被引:318
作者
Luo, Binbin [1 ,2 ]
Pu, Ying-Chih [4 ]
Lindley, Sarah A. [1 ]
Yang, Yi [1 ]
Lu, Liqiang [1 ,3 ]
Li, Yat [1 ]
Li, Xueming [2 ]
Zhang, Jin Z. [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
[2] Chongqing Univ, Dept Chem & Chem Engn, Chongqing 400044, Peoples R China
[3] China Univ Geosci, Fac Mat Sci & Chem, Wuhan, Peoples R China
[4] Natl Univ Tainan, Dept Mat Sci, Tainan 70005, Taiwan
关键词
(3-aminopropyl)triethoxysilane (APTES); nanocrystals; nanocrystal stability; organolead halide perovskites; photoluminescence; QUANTUM DOTS; HIGH-PERFORMANCE; TEMPERATURE; PASSIVATION; DYNAMICS; GROWTH;
D O I
10.1002/anie.201602236
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CH3NH3PbBr3 perovskite nanocrystals (PNCs) of different sizes (ca. 2.5-100 nm) with high photoluminescence (PL) quantum yield (QY; ca. 15-55%) and product yield have been synthesized using the branched molecules, APTES and NH2-POSS, as capping ligands. These ligands are sterically hindered, resulting in a uniform size of PNCs. The different capping effects resulting from branched versus straight-chain capping ligands were compared and a possible mechanism proposed to explain the dissolution-precipitation process, which affects the growth and aggregation of PNCs, and thereby their overall stability. Unlike conventional PNCs capped with straight-chain ligands, APTES-capped PNCs show high stability in protic solvents as a result of the strong steric hindrance and propensity for hydrolysis of APTES, which prevent such molecules from reaching and reacting with the core of PNCs.
引用
收藏
页码:8864 / 8868
页数:5
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