Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Biointerfaces Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Science. 2020 May 8;368(6491):642-648. doi: 10.1126/science.aaz7949. Epub 2020 Apr 9.
The structural complexity of composite biomaterials and biomineralized particles arises from the hierarchical ordering of inorganic building blocks over multiple scales. Although empirical observations of complex nanoassemblies are abundant, the physicochemical mechanisms leading to their geometrical complexity are still puzzling, especially for nonuniformly sized components. We report the self-assembly of hierarchically organized particles (HOPs) from polydisperse gold thiolate nanoplatelets with cysteine surface ligands. Graph theory methods indicate that these HOPs, which feature twisted spikes and other morphologies, display higher complexity than their biological counterparts. Their intricate organization emerges from competing chirality-dependent assembly restrictions that render assembly pathways primarily dependent on nanoparticle symmetry rather than size. These findings and HOP phase diagrams open a pathway to a large family of colloids with complex architectures and unusual chiroptical and chemical properties.
复合生物材料和生物矿化颗粒的结构复杂性源于无机构建块在多个尺度上的分级有序排列。尽管对复杂纳米组装体的经验观察比比皆是,但导致其几何复杂性的物理化学机制仍然令人费解,特别是对于非均匀尺寸的组件。我们报告了带有半胱氨酸表面配体的多分散金硫醇纳米板自组装成具有螺旋状刺和其他形态的分级组织颗粒(HOP)。图论方法表明,这些 HOP 比其生物对应物具有更高的复杂性。它们复杂的组织来自于竞争的手性依赖性组装限制,这些限制使得组装途径主要取决于纳米颗粒的对称性而不是尺寸。这些发现和 HOP 相图为具有复杂结构和异常手性和化学性质的一大类胶体开辟了道路。