We discuss the treatment of spin-orbit coupling (SOC) in time-reversal-symmetry-broken periodic systems for relativistic electronic structure calculations of materials within the generalized noncollinear Kohn-Sham density functional theory (GKSDFT). We treat SOC self-consistently and express the GKS orbitals in a two-component spinor basis. Crucially, we present a methodology (and its corresponding implementation) for the simultaneous self-consistent treatment of SOC and exact nonlocal Fock exchange operators. The many advantages of the inclusion of nonlocal Fock exchange in the self-consistent treatment of SOC, as practically done in hybrid exchange-correlation functionals, are both formally derived and illustrated through numerical examples: (i) it imparts a local magnetic torque (i.e., the ability of the two-electron potential to locally rotate the magnetization with respect to a starting guess configuration) that is key to converge to the right solution in noncollinear DFT regardless of the initial guess for the magnetization; (ii) because of the local magnetic torque, it improves the rotational invariance of noncollinear formulations of the DFT; (iii) it introduces the dependence on specific pieces of the spinors (i.e., those mapped onto otherwise missing spin blocks of the complex density matrix) into the two-electron potential, which are key to the correct description of the orbital- and spin-current densities and their coupling with the magnetization; and (iv) when space-inversion symmetry is broken, it allows for the full breaking of time-reversal symmetry in momentum space, which would otherwise be constrained by a sum rule linking the electronic band structure at opposite points in the Brillouin zone (k and -k). The presented methodology is implemented in a developmental version of the public CRYSTAL code. Numerical tests are performed on the model system of an infinite radical chain of Ge2H with both space-inversion and time-reversal symmetries broken, which allows to highlight all the above-mentioned effects.
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Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Dept Mat Sci & Engn, Nanjing 210093, Jiangsu, Peoples R ChinaNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
He, Cheng
Sun, Xiao-Chen
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Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Dept Mat Sci & Engn, Nanjing 210093, Jiangsu, Peoples R ChinaNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Sun, Xiao-Chen
Liu, Xiao-Ping
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Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Dept Mat Sci & Engn, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R ChinaNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Liu, Xiao-Ping
Lu, Ming-Hui
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Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Dept Mat Sci & Engn, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R ChinaNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Lu, Ming-Hui
Chen, Yulin
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Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, EnglandNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Chen, Yulin
Feng, Liang
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SUNY Buffalo, Dept Elect Engn, Buffalo, NY 14260 USANanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Feng, Liang
Chen, Yan-Feng
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Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Dept Mat Sci & Engn, Nanjing 210093, Jiangsu, Peoples R China
Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R ChinaNanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China