Cölfen Helmut, Mann Stephen
Max-Planck-Institut für Kolloid- und Grenzflächenforschung, Kolloidchemie, Forschungscampus Golm, 14424 Potsdam, Germany.
Angew Chem Int Ed Engl. 2003 May 30;42(21):2350-65. doi: 10.1002/anie.200200562.
The organization of nanostructures across extended length scales is a key challenge in the design of integrated materials with advanced functions. Current approaches tend to be based on physical methods, such as patterning, rather than the spontaneous chemical assembly and transformation of building blocks across multiple length scales. It should be possible to develop a chemistry of organized matter based on emergent processes in which time- and scale-dependent coupling of interactive components generate higher-order architectures with embedded structure. Herein we highlight how the interplay between aggregation and crystallization can give rise to mesoscale self-assembly and cooperative transformation and reorganization of hybrid inorganic-organic building blocks to produce single-crystal mosaics, nanoparticle arrays, and emergent nanostructures with complex form and hierarchy. We propose that similar mesoscale processes are also relevant to models of matrix-mediated nucleation in biomineralization.
在具有先进功能的集成材料设计中,跨扩展长度尺度的纳米结构组织是一项关键挑战。当前的方法往往基于物理方法,如图案化,而非跨多个长度尺度的构建单元的自发化学组装和转变。应该有可能基于涌现过程开发一种有序物质化学,其中相互作用组分的时间和尺度依赖性耦合会产生具有嵌入式结构的高阶架构。在此,我们强调聚集与结晶之间的相互作用如何导致中尺度自组装以及无机 - 有机混合构建单元的协同转变和重组,从而产生单晶镶嵌体、纳米颗粒阵列以及具有复杂形态和层次结构的涌现纳米结构。我们提出,类似的中尺度过程也与生物矿化中基质介导成核的模型相关。