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dc.contributor.authorLee, Tzu-Yuanen_US
dc.contributor.authorLee, Chi-Youngen_US
dc.contributor.authorChiu, Hsin-Tienen_US
dc.date.accessioned2019-12-13T01:10:04Z-
dc.date.available2019-12-13T01:10:04Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn2470-1343en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acsomega.9b02453en_US
dc.identifier.urihttp://hdl.handle.net/11536/153127-
dc.description.abstractA new synthetic method to grow O-deficient rutile TiO2(s) nanorods (NRs) and nanowires (NWs) by a vapor-solid reaction growth method is developed. TiCl4(g) was employed to react with commercially supplied CaTiO3(s) (size 2-4 mu m) at 973 K under atmospheric pressure to generate TiO2(s) NRs (diameters 80-120 nm, lengths 1-4 mu m). The reaction employing TiCl4(g) and CaO(s) at 973 K also generated CaTiO3(s) (size 4-13 mu m) as the intermediate which reacted further with TiCl4(g) to produce NWs (diameters 80-120 nm, lengths 4-15 mu m). This is the first report of 1D rutile TiO2(s) nanostructure with such a high aspect ratio. Both of the NRs and the NWs, with compositions TiO1.81 and TiO1.65, respectively, were single crystals grown in the [001] direction. Their morphology was affected by the reaction temperature, the concentration of TiCl4(g), and the particle size of CaTiO3(s). The NRs and the NWs were investigated as anode materials for Li+-ion batteries. At constant current rates 1, 2, and 5 C (1 C = 170 mA g-1) for 100 cycles, the cycling (1.0-3.0 V) performance data of the NRs were 146, 123, and 104 mA h g(-1), respectively. On the other hand, the cycling performance data of the NWs were 120, 80, and 52 mA h g(-1), respectively. This is attributed to the high Li+ ion diffusion rate (D-Li(+)) of the NRs (29.52 x 10(-15) cm(2) s(-1)), which exceeds that of the NWs (8.61 x 10(-1)5 cm(2) s(-1)). Although the [001] growth direction of the NR crystals would provide the fastest channels for the diffusion of Li+ ions and enhance the battery capacity, the extremely long channels in the NWs could hamper the diffusion of the Li+ ions. The O-deficiency in the structure would increase the conductivity of the electrode material and improve the stable cycling stability of the batteries also. The long-term cycling test at 2 C for the battery constructed from the NRs retained 121 mA h g(-1) after 200 cycles and 99.2 mA h g(-1) after 800 cycles. The device has an excellent long-term cycling stability with a loss of only 0.04% per cycle.en_US
dc.language.isoen_USen_US
dc.titleVapor-Solid Reaction Growth of Rutile TiO2 Nanorods and Nanowires for Li-Ion-Battery Electrodesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acsomega.9b02453en_US
dc.identifier.journalACS OMEGAen_US
dc.citation.volume4en_US
dc.citation.issue14en_US
dc.citation.spage16217en_US
dc.citation.epage16225en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000489241700053en_US
dc.citation.woscount0en_US
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