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首页> 外文期刊>ACS Omega >Vapor–Solid Reaction Growth of Rutile TiO2 Nanorods and Nanowires for Li-Ion-Battery Electrodes
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Vapor–Solid Reaction Growth of Rutile TiO2 Nanorods and Nanowires for Li-Ion-Battery Electrodes

机译:锂离子电池电极用金红石型TiO2纳米棒和纳米线的汽固反应生长

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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 exceeds that of the NWs (8.61 × 10–15 cm2 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.
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)(尺寸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作为锂离子电池的负极材料。在恒定电流速率1、2和5 C(1 C = 170 mA g-1)下进行100个循环,NR的循环(1.0-3.0 V)性能数据分别为146、123和104 mA hg-1,分别。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NRs的高Li +离子扩散率(DLi +)(29.52×10–15 cm2 s-1),超过了NWs(8.61×10–15 cm2 s-1)。尽管NR晶体的[001]生长方向将为Li +离子的扩散提供最快的通道并增强电池容量,但NW中极长的通道可能会阻碍Li +离子的扩散。该结构中的O-缺乏会增加电极材料的电导率并也改善电池的稳定循环稳定性。由NR制成的电池在2 C下的长期循环测试在200个循环后保持121 mA h g-1,在800个循环后保持99.2 mA h g-1。该器件具有出色的长期循环稳定性,每个循环仅损失0.04%。

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