Expanding the Chemical Versatility of Colloidal Nanocrystals Capped with Molecular Metal Chalcogenide Ligands

被引:255
作者
Kovalenko, Maksym V. [1 ]
Bodnarchuk, Maryna I. [1 ]
Zaumseil, Jana [2 ]
Lee, Jong-Soo [1 ]
Talapin, Dmitri V. [1 ,2 ]
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[2] Argonne Natl Lab, Ctr Nanoscale Mat, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
COORDINATION CHEMISTRY; QUANTUM DOTS; SOLAR-CELLS; ELECTROPHORETIC MOBILITY; MAGNETIC-RESONANCE; CRYSTAL-STRUCTURES; ZINTL ANIONS; CDSE; SURFACE; NANOPARTICLES;
D O I
10.1021/ja1024832
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed different strategies toward the synthesis of colloidal nanocrystals stabilized with molecular metal chalcogenide complexes (MCCs). Negatively charged MCCs, such as SnS44-, Sn2S64-, SnTe44-, AsS33-, MoS42-, can quantitatively replace the organic ligands at the nanocrystal surface and stabilize nanocrystal solutions in different polar media. We showed that all-inorganic nanocrystals composed of metals, semiconductors, or magnetic materials and capped with various MCC ligands can be synthesized using convenient and inexpensive chemicals and environmentally benign solvents such as water, formamide, or dimethylsulfoxide. The development of mild synthetic routes was found to be crucial for the design of highly luminescent all-inorganic nanocrystals, such as CdSe/ZnS and PbS capped with Sn2S64- MCCs, respectively. We also prepared conductive and luminescent layer-by-layer assemblies from inorganically capped colloidal nanocrystals and polyelectrolytes. In close-packed films of 5-nm Au nanocrystals stabilized with Na2Sn2S6 we observed very high electrical conductivities (>1000 S cm(-1)).
引用
收藏
页码:10085 / 10092
页数:8
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