Largely Enhanced Ferromagnetism in Bare CuO Nanoparticles by a Small Size Effect

被引:21
作者
Batsaikhan, Erdembayalag [1 ,3 ]
Lee, Chi-Hung [1 ]
Hsu, Han [1 ]
Wu, Chun-Ming [2 ]
Peng, Jen-Chih [2 ]
Ma, Ma-Hsuan [1 ]
Deleg, Sangaa [3 ]
Li, Wen-Hsien [1 ]
机构
[1] Natl Cent Univ, Dept Phys, Jhongli 32001, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[3] Mongolian Acad Sci, Inst Phys & Technol, Ulaanbaatar 13330, Mongolia
关键词
ROOM-TEMPERATURE FERROMAGNETISM; FIELD-EMISSION; OXIDE; DEPENDENCE; GAP;
D O I
10.1021/acsomega.9b02913
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnetic properties of fully oxygenated bare CuO nanoparticles have been investigated using magnetization, X-ray diffraction, neutron diffraction, and Raman scattering measurements. The Langevin field profile is clearly revealed in the isothermal magnetization of 8.8 nm CuO nanoparticle assembly even at 300 K, revealing a 172 times enhancement of the ferromagnetic responses over that of bulk CuO. Surface magnetization of 8.8 nm CuO reaches 18% of the core magnetization. The Cu spins in 8.8 nm CuO order below 400 K, which is 1.7 times higher than the 231 K observed in bulk CuO. A relatively simple magnetic structure that may be indexed using a modulation vector of (0.2, 0, 0.2) was found for the 8.8 nm CuO, but no magnetic incommensurability was observed in bulk CuO. The Cu spins in 8.8 nm CuO form spin density waves with length scales of 5 chemical unit cells long along the crystallographic a- and c-axis directions. Considerable amounts of electronic charge shift from around the Cu lattice sites toward the interconnecting regions of two neighboring Cu-Cu ions, resulting in a stronger ferromagnetic direct exchange interaction for the neighboring Cu spins in 8.8 nm CuO.
引用
收藏
页码:3849 / 3856
页数:8
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