纳米晶
成核
材料科学
纳米技术
胶体
化学物理
自组装
亚稳态
相(物质)
量子点
化学工程
化学
物理化学
工程类
有机化学
作者
Igor Coropceanu,Eric M. Janke,Joshua Portner,Danny Haubold,Trung Dac Nguyen,Avishek Das,Christian Tanner,James K. Utterback,Samuel W. Teitelbaum,Margaret H. Hudson,Nivedina A. Sarma,Alex Hinkle,Christopher J. Tassone,Alexander Eychmüller,David T. Limmer,Mónica Olvera de la Cruz,Naomi S. Ginsberg,Dmitri V. Talapin
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-03-24
卷期号:375 (6587): 1422-1426
被引量:124
标识
DOI:10.1126/science.abm6753
摘要
Colloidal nanocrystals of metals, semiconductors, and other functional materials can self-assemble into long-range ordered crystalline and quasicrystalline phases, but insulating organic surface ligands prevent the development of collective electronic states in ordered nanocrystal assemblies. We reversibly self-assembled colloidal nanocrystals of gold, platinum, nickel, lead sulfide, and lead selenide with conductive inorganic ligands into supercrystals exhibiting optical and electronic properties consistent with strong electronic coupling between the constituent nanocrystals. The phase behavior of charge-stabilized nanocrystals can be rationalized and navigated with phase diagrams computed for particles interacting through short-range attractive potentials. By finely tuning interparticle interactions, the assembly was directed either through one-step nucleation or nonclassical two-step nucleation pathways. In the latter case, the nucleation was preceded by the formation of two metastable colloidal fluids.
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