How To Control the Crystalline Structure of Supracrystals of 5-nm Silver Nanocrystals

被引:44
作者
Courty, Alexa [1 ]
Richardi, Johannes [1 ]
Albouy, Pierre-Antoine [2 ]
Pileni, Marie-Paule [1 ]
机构
[1] Univ Paris 06, CNRS, Lab Mat Mesoscop & Nanometr LM2N, UMR 7070, F-75252 Paris 05, France
[2] Univ Paris 11, CNRS, Lab Phys Solides, UMR 8502, F-91405 Orsay, France
关键词
silver nanocrystals; crystalline structure; 3D self-assembly; computational chemistry; SUPRA-CRYSTALS; SELF-ORGANIZATION; STERIC STABILIZATION; COBALT NANOCRYSTALS; MAGNETIC-PROPERTIES; OXIDE NANOCRYSTALS; SUPERLATTICES; GOLD; NANOPARTICLES; PARTICLES;
D O I
10.1021/cm201313r
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Supracrystals of 5-nm silver nanocrystals are characterized by various structures, ranging from face-centered-cubic (fcc), to hexagonal-close-packed (hcp), to body-centered-cubic (bcc) structures. Here, it is shown that the transition from fcc to hcp is solvent-dependent and attributed to specific stacking processes, depending on the evaporation kinetics. Hence, at a fixed substrate temperature, the most volatile solvents (such as hexane and toluene) favor the growth of fcc superlattices, whereas with solvents that have a higher boiling point (such as octane, decane, and dodecane), hcp supracrystals are produced. In contrast, the formation of bcc structures is shown to be solvent-independent and is attributed to van der Waals attractions. The chain length of the coating agent and the deposition temperature govern the transition from compact (fcc/hcp) to bcc supracrystals. The experimentally phase transitions are interpreted by theoretical approaches.
引用
收藏
页码:4186 / 4192
页数:7
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