Electrochemical deposition of Co nanowire arrays; quantitative consideration of concentration profiles

被引:83
作者
Valizadeh, S
George, JM
Leisner, P
Hultman, L
机构
[1] ACREO AB, Interconnect & Packaging, S-60221 Norrkoping, Sweden
[2] Ctr Natl Rech Sci & Thomson, UMR, Lab Cent Rech Thomson, F-91404 Orsay, France
[3] Linkoping Univ, Dept Phys, Thin Film Phys Div, S-58183 Linkoping, Sweden
关键词
nanodes; spherical diffusion; magnetic properties; nanostructures;
D O I
10.1016/S0013-4686(01)00797-6
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrodeposition of Co into ion track etched polycarbonate membranes by a chronoamperometric method has been studied. The concentration variation and diffusion limiting current during nanoprocessing for growth of Co in nanoelectrode applications are described for two regimes; in the vicinity of the electrode and at the mouth of pores. The behaviour of the as-deposited nanoelectrodes can be modelled as a recessed microelectrode. A diffusion controlled limiting current of the nanodes is studied by the Cottrell equation at short times, i.e. current alphat(-1/2), At longer times, a steady-state current is obtained due to gradually increasing radii, r, of the spherical diffusion zones from each recessed nanode, i.e. current alpha (1/(r + L)), where L is the membrane thickness. The experimental value of diffusion coefficient D for Co ions was found: D = 2.5 x 10(-5) cm(2) s(-1). XRD and TEM measurements on 250 nm diameter and 20 mum long Co nanowires showed a hexagonal closed packed phase with a < 100 > texturing. The nanowires exhibited an enhanced magnetic coercivity in comparison to bulk Co. The difference of saturation fields between the parallel and perpendicular orientation fields corresponds well to the expected demagnetisation field of 2 piM = 8796 Oe value due to the shape anisotropy in case of an infinite thin Co cylinder. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:865 / 874
页数:10
相关论文
共 18 条
[1]  
AIMAWLAWI D, 1991, J APPL PHYS, V70, P4421
[2]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[3]   ELECTROCHEMISTRY IN ORGANIC-SOLVENTS WITHOUT SUPPORTING ELECTROLYTE USING PLATINUM MICROELECTRODES [J].
BOND, AM ;
FLEISCHMANN, M ;
ROBINSON, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 168 (1-2) :299-312
[4]   THEORY OF ELECTROCHEMICAL PROCESSES AT AN INLAID DISK MICROELECTRODE UNDER STEADY-STATE CONDITIONS [J].
BOND, AM ;
OLDHAM, KB ;
ZOSKI, CG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 245 (1-2) :71-104
[5]   MAGNETIC-ANISOTROPY OF ELECTRODEPOSITED COBALT ON ALUMITE SUBSTRATE [J].
CHENG, TJ ;
JORNE, J ;
GAU, JS .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (01) :93-95
[6]   HEAVY-ION TRACKS IN POLYCARBONATE - COMPARISON WITH A HEAVY-ION IRRADIATED MODEL-COMPOUND (DIPHENYL CARBONATE) [J].
FERAIN, E ;
LEGRAS, R .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 1993, 82 (04) :539-548
[7]   POTENTIOSTATIC STUDIES OF ELECTROCHEMICAL NUCLEATION [J].
GUNAWARDENA, GA ;
HILLS, GJ ;
MONTENEGRO, I .
ELECTROCHIMICA ACTA, 1978, 23 (08) :693-697
[8]   DIFFUSION CURRENT AT MICRODISK ELECTRODES - APPLICATION TO ACCURATE MEASUREMENT OF DIFFUSION-COEFFICIENTS [J].
KAKIHANA, M ;
IKEUCHI, H ;
SATO, GP ;
TOKUDA, K .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1981, 117 (02) :201-211
[9]  
KHOMTOV NE, 1969, ELECTROCHEMISTRY ELE
[10]  
MARTIN CR, 1994, SCIENCE, V266, P196