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Ferromagnetic Ge1−xMx (M = Mn, Fe, and Co) Nanowires

Authors
Cho, Yong JaeKim, Chang HyunKim, Han SungLee, Wang SuPark, Seong-HunPark, JeungheeBae, Seung YongKim, BongsooLee, HangilKim, Jae-Young
Issue Date
Jul-2008
Publisher
ACS
Citation
Chemistry of Materials, v.20, no.14, pp 4694 - 4702
Pages
9
Journal Title
Chemistry of Materials
Volume
20
Number
14
Start Page
4694
End Page
4702
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148196
DOI
10.1021/cm7035635
ISSN
0897-4756
Abstract
We synthesized Ge and Ge1−xMx (M = Mn, Co, and Fe, x ≤ 0.4) nanowires using the thermal vapor transport method. All of the nanowires consisted of single-crystalline Ge nanocrystals grown uniformly with the [111] direction. High-resolution X-ray diffraction showed no metal cluster formation for any of the Ge1−xMx nanowires, and the reduction of the lattice constant for the Mn-substituted nanowires. X-ray absorption spectroscopy and X-ray magnetic circular dichroism measurements revealed that the Mn2+ ions preferentially occupy the tetrahedral sites, substituting for Ge. The magnetic moment of the Mn ions reaches a maximum for x = 0.1, which is much larger than that of the Fe or Co ions. The magnetic hysteresis confirms the room-temperature ferromagnetism of the Ge1−xMnx nanowires, which is also maximized at x = 0.1. We suggest that the Mn ions produce dopant−acceptor hybridization with host defects in the p-type Ge nanowires. The Mn substitution is more effective to form significant ferromagnetic Ge nanowires, compared to the Fe or Co substitution.
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