Erjun Kan

Erjun Kan

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 December 2015 in Angewandte Chemie International Edition
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Journal Article
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SZShengli Zhang
Shengli Zhang
MXMeiqiu Xie
Meiqiu Xie
FLFengyu Li
Fengyu Li
ZYZhong Yan
Zhong Yan
YLYafei Li
Yafei Li
Haibo ZengHaibo Zeng
Haibo Zeng

11 March 2008 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
EKErjun Kan
Erjun Kan
ZLZhenyu Li
Zhenyu Li
JYJinlong Yang
Jinlong Yang
JHJ. G. Hou
J. G. Hou

27 December 2011 in Physical Review B
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Journal Article
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HXHongjun Xiang
Hongjun Xiang
EKErjun Kan
Erjun Kan
SWSu-Huai Wei
Su-Huai Wei
MWM.-H. Whangbo
M.-H. Whangbo
XGX. G. Gong
X. G. Gong
A novel general method of describing the spin-lattice interactions in magnetic solids is proposed in terms of first-principles calculations. The spin exchange and Dzyaloshinskii-Moriya interactions, as well as their derivatives with respect to atomic displacements, can be evaluated efficiently on the basis of density-functional calculations for four ordered spin states. By taking into consideration the spin-spin interactions, the phonons, and the coupling between them, we show that the ground-state structure of a representative spin-frustrated spinel, MgCr2O4, is tetragonally distorted, in agreement with experiments. However, our calculations find the lowest energy for the collinear spin ground state, in contrast to previously suggested noncollinear models.

21 August 2018 in Journal of the American Chemical Society
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Journal Article
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CHChengxi Huang
Chengxi Huang
JFJunsheng Feng
Junsheng Feng
FWFang Wu
Fang Wu
DADildar Ahmed
Dildar Ahmed
BHBing Huang
Bing Huang
EKErjun Kan
Erjun Kan

2 April 2018 in Physical Review Letters
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CHChengxi Huang
Chengxi Huang
YDYongping Du
Yongping Du
HWHaiping Wu
Haiping Wu
HXHongjun Xiang
Hongjun Xiang
KDKaiming Deng
Kaiming Deng
EKErjun Kan
Erjun Kan
The realization of multiferroics in nanostructures, combined with a large electric dipole and ferromagnetic ordering, could lead to new applications, such as high-density multistate data storage. Although multiferroics have been broadly studied for decades, ferromagnetic ferroelectricity is rarely explored, especially in two-dimensional (2D) systems. Here we report the discovery of 2D ferromagnetic ferroelectricity in layered transition-metal halide systems. On the basis of first-principles calculations, we reveal that a charged CrBr3 monolayer exhibits in-plane multiferroicity, which is ensured by the combination of orbital and charge ordering as realized by the asymmetric Jahn-Teller distortions of octahedral Cr─Br6 units. As an example, we further show that (CrBr3)2Li is a ferromagnetic ferroelectric multiferroic. The explored phenomena and mechanism of multiferroics in this 2D system not only are useful for fundamental research in multiferroics but also enable a wide range of applications in nanodevices.

10 December 2007 in Applied Physics Letters
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Journal Article
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EKErjun Kan
Erjun Kan
ZLZhenyu Li
Zhenyu Li
JYJinlong Yang
Jinlong Yang
JHJ. G. Hou
J. G. Hou
At B3LYP level of theory, we predict that the half-metallicity in zigzag edge graphene nanoribbon (ZGNR) can be realized when an external electric field is applied across the ribbon. The critical electric field decreases with the increase of the ribbon width to induce the half-metallicity. Both the spin polarization and half-metallicity are removed when the edge state electrons fully transferred from one side to the other under very strong electric field. The electric field range under which ZGNR remains half-metallic increases with the ribbon width. Our study demonstrates a rich field-induced spin polarization behavior, which may lead to some important applications in spinstronics.