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Vapor–Solid Reaction Growth of Rutile TiO2 Nanorodsand Nanowires for Li-Ion-Battery Electrodes

机译:金红石型TiO2纳米棒的汽固反应生长和用于锂离子电池电极的纳米线

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摘要

A 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 μm) at 973 K under atmospheric pressure to generate TiO2(s) NRs (diameters 80–120 nm, lengths 1–4 μm). The reaction employing TiCl4(g) and CaO(s) at 973 K also generated CaTiO3(s) (size 4–13 μm) as the intermediate which reacted further with TiCl4(g) to produce NWs (diameters 80–120 nm, lengths 4–15 μm). 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 (DLi+) of the NRs (29.52 × 10–15 cm2 s–1), which exceedsthat of the NWs (8.61 × 10–15 cm2 s–1). Although the [001] growth direction of theNR crystals would provide the fastest channels for the diffusion ofLi+ ions and enhance the battery capacity, the extremelylong channels in the NWs could hamper the diffusion of the Li+ ions. The O-deficiency in the structure would increase theconductivity of the electrode material and improve the stable cyclingstability of the batteries also. The long-term cycling test at 2 Cfor 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 lossof only 0.04% per cycle.
机译:开发了一种新的通过汽固反应生长法生长缺氧的金红石型TiO2(s)纳米棒(NRs)和纳米线(NWs)的合成方法。 TiCl4(g)用于在大气压力下于973 K下与市售的CaTiO3(尺寸2–4μm)反应,生成TiO2(s)NR(直径80-120 nm,长度1-4μm)。在973 K下使用TiCl4(g)和CaO(s)的反应还生成了CaTiO3(s)(大小为4–13μm)作为中间体,进一步与TiCl4(g)反应生成NW(直径80-120 nm,长度) 4-15微米)。这是具有高纵横比的一维金红石型TiO2纳米结构的首次报道。分别具有组成TiO1.81和TiO1.65的NR和NW均为沿[001]方向生长的单晶。它们的形态受反应温度,TiCl4(g)的浓度和CaTiO3(s)的粒径的影响。研究了NRs和NWs作为Li + 离子电池的负极材料。在1、2和5 C恒定电流速率下(1 C = 170 mA g –1 )持续100个循环,NR的循环(1.0–3.0 V)性能数据为146、123,和104 mA hg –1 。另一方面,NW的循环性能数据分别为120、80和52 mA h g –1 。这归因于NR的高Li + 离子扩散率(DLi + )(29.52×10 –15 cm 2 s –1 ),超过NWs(8.61×10 –15 cm 2 s –1 )。尽管[001]的增长方向NR晶体将提供最快的通道扩散Li + 离子可增强电池容量NWs中的长通道可能会阻碍Li + 离子的扩散。结构中的O缺陷会增加电极材料的电导率并改善稳定循环电池也稳定。 2 C的长期循环测试由NR制成的电池在200次循环后保留121 mA h g -1 ,在800次循环后保留99.2 mA h g -1 。该器件具有出色的长期循环稳定性,但损耗小每个周期只有0.04%。

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