Hierarchically organized CNT@TiO 2 @Mn 3 O 4 nanostructures for enhanced lithium storage performance
Here a new concept is conceived to design CNT@TiO 2 @Mn 3 O 4 nanostructures, in which CNTs, TiO 2 nanosheets and Mn 3 O 4 nanoparticles are hierarchically organized in a three-stage order. In this concept, each component plays a unique, indispensable role. In the first stage, 1D CNTs serve not only...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2017, Vol.5 (32), p.17048-17055 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Here a new concept is conceived to design CNT@TiO 2 @Mn 3 O 4 nanostructures, in which CNTs, TiO 2 nanosheets and Mn 3 O 4 nanoparticles are hierarchically organized in a three-stage order. In this concept, each component plays a unique, indispensable role. In the first stage, 1D CNTs serve not only as a backbone to accommodate mechanical stress, but also as a conductive dopant to facilitate electron transport. In the second stage, 2D TiO 2 nanosheets act as a major active material to ensure high safety and a long cycle life. In the third stage, 0D Mn 3 O 4 nanoparticles function as an auxiliary active material to contribute an extraordinarily high theoretical capacity. Besides, the CNTs can minimize the restacking of the TiO 2 nanosheets, thus guaranteeing good structural integrity. TiO 2 nanosheets, being flexible and elastic in nature, are able to inhibit the aggregation of Mn 3 O 4 nanoparticles, as well as buffer the volume variation suffered during repeated lithiation/delithiation. Mn 3 O 4 nanoparticles, in turn, are capable of physically isolating the TiO 2 nanosheets to enlarge their interlayer distances for easy lithium and electron access. Thanks to the significant synergy, CNT@TiO 2 @Mn 3 O 4 nanostructures exhibit enhanced cycle and rate performances and represent a new step towards high-performance anode candidates of lithium-ion batteries. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C7TA02823G |