材料科学
树枝状大分子
软物质
纳米技术
纳米结构
自组装
纳米颗粒
纳米尺度
化学物理
晶格常数
晶体结构
结晶学
衍射
化学
胶体
物理化学
高分子化学
物理
光学
作者
Ville Liljeström,Jani Seitsonen,Mauri A. Kostiainen
出处
期刊:ACS Nano
[American Chemical Society]
日期:2015-10-24
卷期号:9 (11): 11278-11285
被引量:80
标识
DOI:10.1021/acsnano.5b04912
摘要
Atomic crystal structure affects the electromagnetic and thermal properties of common matter. Similarly, the nanoscale structure controls the properties of higher length-scale metamaterials, for example, nanoparticle superlattices and photonic crystals. Electrostatic self-assembly of oppositely charged nanoparticles has recently become a convenient way to produce crystalline nanostructures. However, understanding and controlling the assembly of soft nonmetallic particle crystals with long-range translational order remains a major challenge. Here, we show the electrostatic self-assembly of binary soft particle cocrystals, consisting of apoferritin protein cages and poly(amidoamine) dendrimers (PAMAM), with very large crystal domain sizes. A systematic series of PAMAM dendrimers with generations from two to seven were used to produce the crystals, which showed a dendrimer generation dependency on the crystal structure and lattice constant. The systematic approach presented here offers a transition from trial-and-error experiments to a fundamental understanding and control over the nanostructure. The structure and stability of soft particle cocrystals are of major relevance for applications where a high degree of structural control is required, for example, protein-based mesoporous materials, nanoscale multicompartments, and metamaterials.
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