Mica-like vanadium pentoxide-nanostructured thin film as high-performance cathode for lithium-ion batteries

被引:16
作者
Yu, Danmei [1 ]
Qiao, Yajuan [1 ]
Zhou, Xiaoyuan [2 ]
Wang, Jie [1 ]
Li, Chao [1 ]
Chen, Changguo [1 ]
Huo, Qisheng [3 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Sch Phys, Chongqing 400044, Peoples R China
[3] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Mica-like; Nanostructure; Vanadium pentoxide; Thin film; Lithium-ion batteries; Cathode materials; HIGH-POWER; ELECTROCHEMICAL PROPERTIES; COBALT OXIDE; V2O5; CATHODE; ELECTRODES; INTERCALATION; GELS;
D O I
10.1016/j.jpowsour.2014.04.099
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Stable and homogeneous mica-like vanadium pentoxide (V2O5)-nanostructured thin films are prepared directly by simple anodic deposition from V2O5/H2O2 sol solution, and then dried at ambient temperature and annealed at 500 degrees C in air for 1 h. The films' crystal- and microstructures, surface morphology and Li-ion intercalation properties were characterized and analyzed by X-Ray diffraction (XRD), field emission scanning electron microscopy (FSEM), thermogravimetric analysis (TGA), and electrochemical techniques. When used as a lithium-ion battery (LIB) cathode, the films exhibit a large discharge capacity of 596 mAh g(-1) at a current density of 1080 mA g(-1), as well as excellent cyclic stability and a fading rate of 1% per cycle. Explanations for such significant enhancements in specific capacity, cyclic stability, and rate performance of mica-like V2O5-nanostructured thin films are demonstrated in this study. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 30 条
  • [1] Aluminum-doped lithium nickel cobalt oxide electrodes for high-power lithium-ion batteries
    Chen, CH
    Liu, J
    Stoll, ME
    Henriksen, G
    Vissers, DR
    Amine, K
    [J]. JOURNAL OF POWER SOURCES, 2004, 128 (02) : 278 - 285
  • [2] Atomic Layer Deposition of LiCoO2 Thin-Film Electrodes for All-Solid-State Li-Ion Micro-Batteries
    Donders, M. E.
    Arnoldbik, W. M.
    Knoops, H. C. M.
    Kessels, W. M. M.
    Notten, P. H. L.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2013, 160 (05) : A3066 - A3071
  • [3] Synthesis and electrochemical properties of layered LiNi0.5-xMn0.5-xCo2xO2 for lithium-ion battery from nickel manganese cobalt oxide precursor
    Dou, Shumei
    Wang, Wenlou
    [J]. JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2011, 15 (02) : 399 - 404
  • [4] Vanadia gel synthesis via peroxovanadate precursors.: 1.: In situ laser Raman and 51V NMR characterization of the gelation process
    Fontenot, CJ
    Wiench, JW
    Pruski, M
    Schrader, GL
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (49): : 11622 - 11631
  • [5] Novel ε-Cu0.95V2O5 hollow microspheres and α-CuV2O6 nanograins: Facile synthesis and application in lithium-ion batteries
    Hu, Wen
    Du, Xinchuan
    Wu, Yaoming
    Wang, Limin
    [J]. JOURNAL OF POWER SOURCES, 2013, 237 : 112 - 118
  • [6] 3-V AND 4-V LITHIUM MANGANESE OXIDE CATHODES FOR RECHARGEABLE LITHIUM BATTERIES
    HUANG, HT
    BRUCE, PG
    [J]. JOURNAL OF POWER SOURCES, 1995, 54 (01) : 52 - 57
  • [7] Electrochemical properties of spherically shaped dense V2O5 cathode powders prepared directly by spray pyrolysis
    Ko, You Na
    Kim, Jung Hyun
    Choi, Seung Ho
    Kang, Yun Chan
    [J]. JOURNAL OF POWER SOURCES, 2012, 211 : 84 - 91
  • [8] Dependence of electrochemical properties of vanadium oxide films on their nano- and microstructures
    Lee, K
    Wang, Y
    Cao, GH
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (35) : 16700 - 16704
  • [9] Roles of nanosize in lithium reactive nanomaterials for lithium ion batteries
    Lee, Kyu Tae
    Cho, Jaephil
    [J]. NANO TODAY, 2011, 6 (01) : 28 - 41
  • [10] VANADIUM PENTOXIDE GELS .2. STRUCTURAL STUDY BY X-RAY-DIFFRACTION
    LEGENDRE, JJ
    ALDEBERT, P
    BAFFIER, N
    LIVAGE, J
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1983, 94 (01) : 84 - 89