Magnetization reversal dependence on effective magnetic anisotropy in electroplated Co–Cu nanowire arrays

2015 ◽  
Vol 3 (18) ◽  
pp. 4688-4697 ◽  
Author(s):  
J. García ◽  
V. M. Prida ◽  
L. G. Vivas ◽  
B. Hernando ◽  
E. D. Barriga-Castro ◽  
...  

Arrays of Co(100−x)Cu(x) (0 ≤ x ≤ 27) nanowires with 45 nm of diameter and 18 μm in length, have been potentiostatically electrodeposited into the hexagonally self-assembled nanopores of anodic alumina membranes.

2001 ◽  
Vol 16 (4) ◽  
pp. 1138-1144 ◽  
Author(s):  
Y. Lei ◽  
L. D. Zhang

Highly ordered TiO2 nanowire arrays were prepared in anodic alumina membranes by a sol-gel method. The nanowires are single-crystalline anatase phase with uniform diameters around 50 nm. At room temperature, photoluminescence (PL) measurements of these TiO2 nanowire arrays showed a visible broad band with three peaks, which were located at about 425, 460, and 530 nm that are attributed to self-trapped excitons, F, and F+ centers, respectively. A model is also presented to explain the PL intensity drop-down of the TiO2 nanowire arrays embedded in the alumina membrane: the blue PL band of the anodic alumina membranes arises from the F+ centers on the pore walls, and the TiO2 nanowires first form in the center area of the pores and then extend to the pore walls.


2010 ◽  
Vol 2010 ◽  
pp. 1-4 ◽  
Author(s):  
Youwen Yang ◽  
Yanbiao Chen ◽  
Yucheng Wu ◽  
Xiangying Chen ◽  
Mingguang Kong

The Co nanowires with different diameters were prepared by pulsed electrodeposition into anodic alumina membranes oxide templates. The micrographs and crystal structures of nanowires were studied by FE-SEM, TEM, and XRD. Due to their cylindrical shape, the nanowires exhibit perpendicular anisotropy. The coercivity and loop squareness (Mr/Ms) of Co nanowires depend strongly on the diameter. Both coercivity and Mr/Ms decrease with increasing wire diameter. The behavior of the nanowires is explained briefly in terms of localized magnetization reversal.


2002 ◽  
Vol 14 (17) ◽  
pp. 1227-1230 ◽  
Author(s):  
Y. Zhang ◽  
G. Li ◽  
Y. Wu ◽  
B. Zhang ◽  
W. Song ◽  
...  

2008 ◽  
Vol 254 (13) ◽  
pp. 3845-3848 ◽  
Author(s):  
Xiaoye Hu ◽  
Zhenyang Wang ◽  
Tianci Zhang ◽  
Xiaoyan Zeng ◽  
Wei Xu ◽  
...  

2001 ◽  
Vol 339 (3-4) ◽  
pp. 174-178 ◽  
Author(s):  
Y.W. Wang ◽  
G.W. Meng ◽  
C.H. Liang ◽  
G.Z. Wang ◽  
L.D. Zhang

2001 ◽  
Vol 674 ◽  
Author(s):  
M. Kröll ◽  
L. J. de Jongh ◽  
F. Luis ◽  
P. Paulus ◽  
G. Schmid

ABSTRACTThe magnetization reversal and magnetic anisotropy of Fe, Ni and Co nanowires is studied at low temperatures. All nanowires show a strong shape anisotropy with the easy axis being parallel to the long axis of the wires. Co nanowires additionally show a temperature dependent magnetocrystalline anisotropy along the hexagonal c-axis, which is directed nearly perpendicular to the long axis of the wires, as is confirmed by X-Ray diffraction measurements [1] and reported by Strijkers et al. who performed NMR measurements on samples prepared in a similar way [2]. Therefore, at low temperatures and for large wire diameters a competition between magnetocrystalline and shape anisotropies can be observed. Co wires with a small diameter, however, do not show a significant magnetocrystalline anisotropy. Fcc-Co, which is only known as a high-temperature Co modification and which does not have a large magnetocrystalline anisotropy constant, becomes the predominant Co modification here [1,3]. Investigations on the size dependence of the switching field for Fe and Ni nanowires provide information about the magnetization reversal process, which takes place via a nucleation of small magnetic domains probably at the end of the wires, and subsequent propagation of the domain wall along the wire.


2005 ◽  
Vol 80 (8) ◽  
pp. 1701-1706 ◽  
Author(s):  
M. Hernández-Vélez ◽  
K.R. Pirota ◽  
F. Pászti ◽  
D. Navas ◽  
A. Climent ◽  
...  

2012 ◽  
Vol 135 (1) ◽  
pp. 77-81 ◽  
Author(s):  
Yantao Pang ◽  
Baojin Zhang ◽  
Junqing Zhao ◽  
Jie Wang ◽  
Yanqi Wu

Sign in / Sign up

Export Citation Format

Share Document