About this book
This book presents wet chemical sol-gel and hydrothermal methods for 1D oxide nanostructure preparation. These methods represent an attractive route to multifunctional nanomaterials synthesis, as they are versatile, inexpensive and, thus, appropriate for obtaining a wide range of oxide materials with tailored morphology and properties. Three specific oxides (SiO2, TiO2, ZnO) are discussed in detail in order to illustrate the principle of the sol-gel and hydrothermal preparation of 1D oxide nanostructures. Other oxides synthesized via this method are also briefly presented.
Throughout the book, the correlation between the tubular structure and the physico-chemical properties of these materials is highlighted. 1D oxide nanostructures exhibit interesting optical and electrical properties, due to their confined morphology. In addition, a well-defined geometry can be associated with chemically active species. For example, the pure SiO2 nanotubes presented a slight photocatalytic activity, while the Pt-doped SiO2 tubular materials act as microreactors in catalytic reactions. In the case of titania and titanate nanotubes, large specific surface area and pore volume, ion-exchange ability, enhanced light absorption, and fast electron-transport capability have attracted significant research interest. The chemical and physical modifications (microwave assisted hydrothermal methods) discussed here improve the formation kinetics of the nanotubes. The ZnO nanorods/tubes were prepared as random particles or as large areas of small, oriented 1D ZnO nanostructures on a variety of substrates. In the latter case a sol-gel layer is deposited on the substrate prior to the hydrothermal preparation. Using appropriate dopants, coatings of ZnO nanorods with controlled electrical behavior can be obtained.
- DOI https://doi.org/10.1007/978-3-319-32988-8
- Copyright Information The Authors 2016
- Publisher Name Springer, Cham
- eBook Packages Chemistry and Materials Science
- Print ISBN 978-3-319-32986-4
- Online ISBN 978-3-319-32988-8
- Series Print ISSN 2192-1091
- Series Online ISSN 2192-1105
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