The evolution of 'sol-gel' chemistry as a technique for materials synthesis

被引:1071
作者
Danks, A. E. [1 ]
Hall, S. R. [2 ]
Schnepp, Z. [1 ]
机构
[1] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
[2] Univ Bristol, Sch Chem, Complex Funct Mat Grp, Bristol BS8 1TS, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
HIGH-T-C; LUMINESCENT PROPERTIES; COMBUSTION SYNTHESIS; IONIC LIQUIDS; IRON CARBIDE; CITRIC-ACID; OXIDE; NANOPARTICLES; NITRIDE; SILICA;
D O I
10.1039/c5mh00260e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
From its initial use to describe hydrolysis and condensation processes, the term 'sol-gel' is now used for a diverse range of chemistries. In fact, it is perhaps better defined more broadly as covering the synthesis of solid materials such as metal oxides from solution-state precursors. These can include metal alkoxides that crosslink to form metal-oxane gels, but also metal ion-chelate complexes or organic polymer gels containing metal species. What is important across all of these examples is how the choice of precursor can have a significant impact on the structure and composition of the solid product. In this review, we will attempt to classify different types of sol-gel precursor and how these can influence a sol-gel process, from self-assembly and ordering in the initial solution, to phase separation during the gelation process and finally to crystallographic transformations at high temperature.
引用
收藏
页码:91 / 112
页数:22
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