Analysis of electrical-field-dependent Dzyaloshinskii-Moriya interaction and magnetocrystalline anisotropy in a two-dimensional ferromagnetic monolayer

2018 ◽  
Vol 97 (5) ◽  
Author(s):  
Jie Liu ◽  
Mengchao Shi ◽  
Jiwu Lu ◽  
M. P. Anantram
2011 ◽  
Vol 32 (5) ◽  
pp. 605-607 ◽  
Author(s):  
Jiaqi Yang ◽  
Jingfeng Yang ◽  
X. Y. Liu ◽  
R. Q. Han ◽  
J. F. Kang ◽  
...  

1998 ◽  
Vol 58 (16) ◽  
pp. 10709-10720 ◽  
Author(s):  
D. Merbach ◽  
E. Schöll ◽  
W. Ebeling ◽  
P. Michler ◽  
J. Gutowski

2015 ◽  
Vol 84 (12) ◽  
pp. 124704 ◽  
Author(s):  
Ágnes Antal ◽  
Titusz Fehér ◽  
Bálint Náfrádi ◽  
László Forró ◽  
András Jánossy

AIP Advances ◽  
2018 ◽  
Vol 8 (5) ◽  
pp. 055316 ◽  
Author(s):  
Jie Liu ◽  
Mengchao Shi ◽  
Pinghui Mo ◽  
Jiwu Lu

2020 ◽  
Vol 101 (18) ◽  
Author(s):  
Jinghua Liang ◽  
Weiwei Wang ◽  
Haifeng Du ◽  
Ali Hallal ◽  
Karin Garcia ◽  
...  

1970 ◽  
Vol 25 (5) ◽  
pp. 627-634 ◽  
Author(s):  
E. G. Weidemann ◽  
G. Zundel

The displacement of the excess charge of the proton in acid solutions is caused by a structure migration of groupings H5O2+ or H9O4+ . The processes which take place during structure migration are discussed on the basis of results gained in IR-investigations. In an electrical field the structure migration is given a preferred direction. The hydrogen bond with the tunneling proton in H5O2+ and the grouping H3O+ in H5O2+ become polarized. Comparison of both polarizabilities demonstrates that, contrary to previous assumptions, the polarization of the hydrogen bond is the field-dependent mechanism. This conclusion is reached upon calculating the polarizability of the hydrogen bond with a symmetrical double minimum potential well. It is shown that the polarizability is extremely large, being approximately two orders of magnitude greater than that of H3O+ . Despite the large polarizability, the shift of the weights of the proton boundary structures is very small for the external fields usually applied in conductivity measurements. It is demonstrated, however, that this slight shift is large enough for the structure diffusion to obtain a preferred direction consistent with the anomalous high proton conductivity.


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