Department of Chemistry, University of Warwick, Coventry, CV4 7AL, UK.
Chem Soc Rev. 2010 Nov;39(11):4303-25. doi: 10.1039/b904702f. Epub 2010 Jun 7.
In this critical review we consider the large literature that has accumulated in the past 5-10 years concerning solution-mediated crystallisation of complex oxide materials using hydrothermal, or more generally solvothermal, reaction conditions. The aim is to show how the synthesis of dense, mixed-metal oxide materials, usually prepared using the high temperatures associated with solid-chemistry, is perfectly feasible from solution in one step reactions, typically at temperatures as low as 200 °C, and that important families of oxide materials have now been reported to crystallise using such synthetic approaches. We will focus on two common structures seen in oxide chemistry, ABO(3) perovskites and A(2)B(2)O(6)O' pyrochlores, and include a systematic survey of the variety of chemical elements now included in these two prototypical structure types, from transition metals, in families of materials that include titanates, niobates, manganites and ferrites, to main-group elements in stannates, plumbates and bismuthates. The significant advantages of solution-mediated crystallisation are well illustrated by the recent literature: examples are provided of elegant control of crystal form from the nanometre to the micron length scale to give thin films, anisotropic crystal morphologies, or hierarchical structures of materials with properties desirable for many important contemporary applications. In addition, new metastable materials have been reported, not stable once high temperatures and pressures are applied and hence not amenable using conventional synthesis. We critically discuss the possible control offered by solvothermal synthesis from crystal chemistry to crystal form and how the discovery of new materials may be achieved. Computer simulation, combinatorial synthesis approaches and in situ methods to follow crystallisation will be vital in providing the predictability in synthesis that is needed for rational design of new materials (232 references).
在这篇评论中,我们回顾了过去 5-10 年中关于使用水热或更一般的溶剂热反应条件下复合氧化物材料的溶液介导结晶的大量文献。目的是展示如何通过一步反应从溶液中制备致密的混合金属氧化物材料,通常使用与固态化学相关的高温,在 200°C 以下的温度下即可实现,并且现在已经报道了许多重要的氧化物材料家族可以使用这种合成方法来结晶。我们将重点介绍氧化物化学中两种常见的结构,ABO(3)钙钛矿和 A(2)B(2)O(6)O' pyrochlore,并对这两种典型结构类型中现在包含的各种化学元素进行系统调查,从过渡金属到主族元素,包括钛酸盐、铌酸盐、锰酸盐和铁酸盐等材料家族中的过渡金属,以及锡酸盐、铅酸盐和铋酸盐中的主族元素。溶液介导结晶的显著优势通过最近的文献得到了很好的说明:从纳米到微米长度尺度的晶体形态的优雅控制的例子提供了对材料的性质有吸引力的薄膜、各向异性晶体形态或分级结构的控制,这些性质对于许多重要的当代应用是理想的。此外,还报道了新的亚稳材料,这些材料在高温高压下不稳定,因此不能使用传统的合成方法制备。我们从晶体化学到晶体形态的角度对溶剂热合成提供的可能控制进行了批判性讨论,并讨论了如何实现新材料的发现。计算机模拟、组合合成方法和原位方法对于提供新的材料合理设计所需的合成可预测性至关重要(232 篇参考文献)。