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首页> 外文期刊>Electrochimica Acta >The electrochemical performanceand multielectron reaction mechanism of NiV2O6 as anovel anode material for lithium-ion batteries
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The electrochemical performanceand multielectron reaction mechanism of NiV2O6 as anovel anode material for lithium-ion batteries

机译:NiV2O6的电化学性能和多电子反应机理作为锂离子电池新型阳极材料

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Based on the existence of multiple valence states of Ni and V, the single-phase nickel vanadium bimetal oxide NiV2O6 is successfully synthesized by asimple sol-gel method. Benefiting from the multielectron reaction of nickel (Ni) and vanadium (V), as novel anode materials of lithium-ion batteries (LIBs), the NiV2O6 electrode exhibits excellent electrochemical performance. After activation, attributed to the decrease in the particle size and an increased pseudocapacitance contribution, the electrode material exhibits a highly stable reversible capacity. At a small current density of 0.1 A g(-1), a stable discharge specific capacity of around 1200 mA h g(-1) can be observed, which is more than three times the capacity of the commercial graphite anode. Using electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) measurement methods, we discuss the function of the activation process. To explore the discharge/charge process, based on in situ X-ray diffraction (XRD) measurements, combined with the X-ray photoelectron spectroscopy (XPS) and SEM results, we analyze the charge/discharge reaction mechanism of the NiV2O6 electrode in detail for the first time. In addition, a full cell is employed to confirm the practicality of the NiV2O6 anode material. (C) 2020 Elsevier Ltd. All rights reserved.
机译:基于Ni和V的多种价态的存在,通过Asimple溶胶 - 凝胶法成功地合成单相镍钒二金属氧化物NiV2O6。受益于镍(Ni)和钒(V)的多电元件反应,作为锂离子电池(Libs)的新型阳极材料,NiV2O6电极表现出优异的电化学性能。在激活之后,归因于粒度的减小和增加的假焦距贡献,电极材料表现出高度稳定的可逆容量。在小电流密度为0.1Ag(-1),可以观察到稳定的放电比容量约为1200mA H(-1),这是商业石墨阳极容量的三倍以上。使用电化学阻抗谱(EIS)和扫描电子显微镜(SEM)测量方法,我们讨论了激活过程的功能。为了探索放电/充电过程,基于原位X射线衍射(XRD)测量,与X射线光电子谱(XPS)和SEM结果相结合,我们详细分析了NIV2O6电极的充电/放电反应机理首次。此外,使用全细胞来证实NIV2O6阳极材料的实用性。 (c)2020 elestvier有限公司保留所有权利。

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