Chemical synthesis of Co/Cu core/shell nanocomposites and evaluation of their magnetic properties

被引:7
作者
Kamal, S. S. Kalyan [1 ]
Sahoo, P. K. [1 ]
Sreedhar, B. [2 ]
Raja, M. Manivel [1 ]
Durai, L. [1 ]
Ram, S. [3 ]
机构
[1] Def Met Res Lab, Hyderabad 500058, Andhra Pradesh, India
[2] Indian Inst Chem Technol, Hyderabad 500007, Andhra Pradesh, India
[3] Indian Inst Technol, Ctr Mat Sci, Kharagpur 721302, W Bengal, India
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2012年 / 177卷 / 14期
关键词
Chemical synthesis; Co/Cu core/shell; Nanocomposites; Magnetic properties; CORE-SHELL NANOPARTICLES; MODIFIED POLYOL PROCESS; HYSTERESIS; IRON;
D O I
10.1016/j.mseb.2012.06.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Co/Cu core/shell nanocomposites (CSNCs) with varying shell thickness were synthesized through a modified polyol process in conjunction with a transmetallation reaction. Tuning of shell thickness was achieved by subtle change in concentration of copper acetate infused in different experiments against a fixed cobalt precursor concentration. Formation of Cu nanoparticles (NPs) was observed from UV-vis spectra, which showed a typical surface plasmon resonance peak at 560 nm. Precise control over particle size was obtained by the use of PVP as stabilizer, which was confirmed by a red shift of 20 cm(-1) in the C=O stretching frequency of various PVP coated Co/Cu CSNCs. Powder x-ray diffraction patterns elucidate the co-existence of distinctive fundamental peaks for both Co and Cu indicating that they have not formed an alloy during the reaction. TEM images corroborate with the above result by revealing the existence of lighter shaded Cu shells coated over dark inner cores of Co. Coalescence of adjacent Cu shells gives a matrix like appearance in case of Co21.2Cu78.8 NPs; whereas Co90.7Cu9.3 NPs were distinctly separated from each other. Magnetic hysteresis loops of all the Co/Cu CSNCs showed ferromagnetic behavior and an increase in magnetization value with decrease in shell thickness was observed. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1200 / 1206
页数:7
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