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Designing Solid Materials from Their Solute State: A Shift in Paradigms toward a Holistic Approach in Functional Materials Chemistry

机译:从溶质状态设计固体材料:范式向功能材料化学整体方法的转变

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摘要

"Non-classical" notions consider formation pathways of crystalline materials where larger species than monomeric chemical constituents, i.e., ions or single molecules, play crucial roles, which are not covered by the classical theories dating back to the 1870s and 1920s. Providing an outline of "non-classical" nucleation, we demonstrate that prenucleation clusters (PNCs) can lie on alternative pathways to phase separation, where the very event of demixing is primarily based on not the sizes of the species forming, as in the classical view, but their dynamics. Rationalizing, on the other hand, that precursors that can be analytically detected in prenucleation stages and that play a role in phase separation must be considered PNCs and cannot be explained by classical notions, we outline a variety of systems where PNCs are important. Indeed, in recent years, with the advent of "non-classical" theories, a primary focus of research concentrated on the fundamental understanding of oligomeric/polymeric and particulate species involved in nucleation and crystallization processes, respectively. At the same time, the near-to unfathomable potential of "non-classical" routes for the synthesis of inorganic functional materials slowly unfolds. An overview of recent developments in the fundamental and mechanistic understanding of "non-classical" nucleation and crystallization in this Perspective then allows us to map out the potential of cluster/particle-driven mineralization pathways to intrinsically tailor the properties of inorganic functional (hybrid) materials via structuration from the nano-to the mesoscale. This is of utter importance for the functionality and performance of materials, as it may even confer emergent properties such as self-healing. Biominerals-often formed via particle accretion mechanisms-demonstrate this impressively and thus can serve as a further source of inspiration how to exploit nonclassical crystallization routes for syntheses of structured and functional materials. These new avenues to synthetic approaches may finally provide a holistic material concept, in which fundamental chemistry and materials science synergistically alloy.
机译:“非经典”的概念考虑了晶体材料的形成途径,其中比单体化学成分更大的物种(即离子或单分子)起着至关重要的作用,这可以追溯到1870年代和1920年代的经典理论中。通过提供“非经典”成核的概述,我们证明了预成核簇(PNC)可以位于相分离的替代途径上,在这种情况下,混合的主要事件主要是基于物种形成的大小,而不是古典观点,但其动力。另一方面,合理化可以在预成核阶段进行分析检测且在相分离中起作用的前体必须视为PNC,而不能用经典概念来解释,我们概述了其中PNC非常重要的各种系统。确实,近年来,随着“非经典”理论的出现,研究的主要重点集中在对分别涉及成核和结晶过程的低聚物/聚合物和颗粒物质的基本理解上。同时,用于合成无机功能材料的“非经典”路线的近乎不可思议的潜力缓慢地展现出来。在此“透视图”中,对“非经典”成核和结晶的基本原理和机理了解的最新进展概述使我们能够绘制出簇/颗粒驱动矿化途径的潜力,以内在地调整无机功能性的特性(混合)材料通过从纳米级到中尺度的结构化。这对于材料的功能和性能非常重要,因为它甚至可以赋予诸如自愈之类的新兴特性。生物矿物(通常是通过颗粒积聚机制形成的)令人印象深刻地证明了这一点,因此可以作为进一步启发灵感的方法,探索如何利用非经典的结晶途径合成结构化和功能性材料。这些合成方法的新途径最终可能会提供一个整体的材料概念,其中基础化学和材料科学将合金协同作用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2019年第11期|4490-4504|共15页
  • 作者

    Gebauer Denis; Wolf Stephan E.;

  • 作者单位

    Univ Konstanz, Dept Chem, Phys Chem, D-78457 Constance, Germany;

    Friedrich Alexander Univ Erlangen Nuremberg, Inst Glass & Ceram, Dept Mat Sci & Engn, D-91058 Erlangen, Germany|Friedrich Alexander Univ Erlangen Nuremberg, Interdisciplinary Ctr Funct Particle Syst, D-91058 Erlangen, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 04:12:48

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