Electrochemical deposition of (Mn, Co)-codoped ZnO nanorod arrays without any template

被引:36
作者
Li, Gao-Ren [1 ]
Qu, Dun-Lin
Zhao, Wen-Xia
Tong, Ye-Xiang
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Peoples R China
[2] Sun Yat Sen Univ, Inst Optoelect & Funct Composite Mat, Guangzhou 510275, Peoples R China
[3] State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China
[4] Sun Yat Sen Univ, Instrumental Anal & Res Ctr, Guangzhou 510725, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrodeposition; zinc oxide; dopant; diluted magnetic semiconductor;
D O I
10.1016/j.elecom.2007.03.012
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
(Mn,Co)-codoped ZnO nanorod arrays were successfully prepared on Cu substrates by electrochemical self-assembly in solution of 0.5 mol/l ZnCl2-0.01 mol/l MnCl2-0.01 mol/1 COCl2-0.1 m01/1 KCl-0.05 mol/l tartaric acid at a temperature of 90 degrees C, and these nanorods were found to be oriented in the c-axis direction with wurtzite structure. Energy dispersive X-ray spectroscopy and x-ray diffraction show that the dopants Mn and Co are incorporated into the wurtzite-structure of ZnO. The concentrations of the dopants, and the orientations and densities of nanorods can easily be well controlled by the current densities of deposition or salt concentrations. Magnetization measurement indicates that the prepared (Mn, Co)-codoped ZnO nanorods with a coercivity of about 91 Oe and a saturation magnetization (M-s) of about 0.23 emu/g. The anisotropic magnetism for the (Mn, Co)-codoped ZnO nanorod arrays prepared in solution of 0.5 mol/l ZnCl2-0.01 mol/l MnCl2-0.01 mol/l COCl2-0.1 mol/l KCl-0.05 mol/l tartaric acid with current density of 0.5 mA/cm(2) was also investigated, and the crossover where the magnetic easy axis switches from parallel to perpendicular occurs at a calculated time of about 112 min. The anisotropic magnetism, depending on the rod geometry and density, can be explained in terms of a competition between self-demagnetization and magnetostatic coupling among the nanorods. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1661 / 1666
页数:6
相关论文
共 28 条
  • [1] Field-effect transistors based on single semiconducting oxide nanobelts
    Arnold, MS
    Avouris, P
    Pan, ZW
    Wang, ZL
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (03) : 659 - 663
  • [2] Optically pumped lasing of ZnO at room temperature
    Bagnall, DM
    Chen, YF
    Zhu, Z
    Yao, T
    Koyama, S
    Shen, MY
    Goto, T
    [J]. APPLIED PHYSICS LETTERS, 1997, 70 (17) : 2230 - 2232
  • [3] Electrodeposition and room temperature ferromagnetic anisotropy of Co and Ni-doped ZnO nanowire arrays
    Cui, JB
    Gibson, UJ
    [J]. APPLIED PHYSICS LETTERS, 2005, 87 (13) : 1 - 3
  • [4] Low-temperature growth and field emission of ZnO nanowire arrays -: art. no. 044315
    Cui, JB
    Daghlian, CP
    Gibson, UJ
    Püsche, R
    Geithner, P
    Ley, L
    [J]. JOURNAL OF APPLIED PHYSICS, 2005, 97 (04)
  • [5] Single-nanowire electrically driven lasers
    Duan, XF
    Huang, Y
    Agarwal, R
    Lieber, CM
    [J]. NATURE, 2003, 421 (6920) : 241 - 245
  • [6] ECINASOROOPESA A, 2001, PHYS REV B, V63, P4415
  • [7] Low-temperature wafer-scale production of ZnO nanowire arrays
    Greene, LE
    Law, M
    Goldberger, J
    Kim, F
    Johnson, JC
    Zhang, YF
    Saykally, RJ
    Yang, PD
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (26) : 3031 - 3034
  • [8] Angular dependence of the coercivity and remanence of ferromagnetic nanowire arrays
    Han, GC
    Zong, BY
    Luo, P
    Wu, YH
    [J]. JOURNAL OF APPLIED PHYSICS, 2003, 93 (11) : 9202 - 9207
  • [9] Room-temperature ultraviolet nanowire nanolasers
    Huang, MH
    Mao, S
    Feick, H
    Yan, HQ
    Wu, YY
    Kind, H
    Weber, E
    Russo, R
    Yang, PD
    [J]. SCIENCE, 2001, 292 (5523) : 1897 - 1899
  • [10] Simple solvothermal route to synthesize ZnO nanosheets, nanonails, and well-aligned nanorod arrays
    Kar, Soumitra
    Dev, Apurba
    Chaudhuri, Subhadra
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (36) : 17848 - 17853