Colloidal Nanocube Supercrystals Stabilized by Multipolar Coulombic Coupling

被引:46
作者
Chan, Henry [2 ]
Demortiere, Arnaud [1 ,3 ]
Vukovic, Lela [2 ]
Kral, Petr [2 ,4 ]
Petit, Christophe [1 ]
机构
[1] Univ Paris 06, Lab Mat Mesoscop & Nanometr, CNRS, UMR 7070, F-75252 Paris 05, France
[2] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[3] Argonne Natl Lab, Ctr Nanoscale Mat, Argonne, IL 60439 USA
[4] Univ Illinois, Dept Phys, Chicago, IL 60607 USA
关键词
molecular dynamics; self-assembly; nanocubes; multipolar coupling; charge transfer; BINARY NANOPARTICLE SUPERLATTICES; NANOCRYSTAL SUPERLATTICES; SELF-ORGANIZATION; GOLD NANOPARTICLES; MOLECULAR-DYNAMICS; CDSE NANOCRYSTALS; BUILDING-BLOCKS; SHAPE; ASSEMBLIES; PARTICLES;
D O I
10.1021/nn3007338
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We explore microscopic principles governing the self-assembly of colloidal octylamine-coated platinum nanocubes solvated In toluene. Our experiments show that regular nanocubes with an edge length of I-RC = 55 nm form supercrystals with simple cubic packing, while slightly truncated nanocubes with an edge length of I-TC = 4.7 nm tend to arrange in fcc packing. We model by averaged force fields and atomistic molecular dynamics simulations the coupling forces between these nanocrystals. Our detailed analysis shows that the fcc packing, which for cubes has a lower density than simple cubic packing, is favored by the truncated nanocubes due to their Coulombic coupling by multipolar electrostatic fields, formed during charge transfer between the octylamine ligands and the Pt cores.
引用
收藏
页码:4203 / 4213
页数:11
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