arXiv subjects

Shuiquan Deng

Publications and source records attributed to Shuiquan Deng.

5 recordsLinked to original sources

arXiv2026

Diagonal Curvature in Second Order Jahn Teller Theory Can Be Negative: An Analytic Proof with First-Principles Confirmation in NH3

We demonstrate that the diagonal curvature in second-order Jahn-Teller theory (SOJTT) can be negative, invalidating its foundational positivity assumption. Using a frozen-phonon many-body expansion, we show no quantum-mechanical principle enforces its positivity; recasting into the Kohn-Sham framework further reveals that phonon-induced eigen-energy changes arise solely from electron-nuclear, Hartree, and exchange-correlation terms, with kinetic-energy contributions canceling identically. First principles calculations on NH3 place the D3h reference configuration at an A2" saddle point; Schwarz-inequality upper-bound analysis confines the HOMO-LUMO mixing contribution to < 0.2% of the total energy drop,while 99.8% originates from the diagonal electron-nuclear term driving N (2s-2pz) electron redistribution. These findings overturn a core SOJTT tenet and establish that spontaneous structural symmetry breaking demands prior verification of a saddle point, not assumed positivity of the diagonal curvature.

cond-mat.mtrl-sci↗

arXiv2026

Mixed Organic Cation in Chiral Two-Dimensional Organic-Inorganic Hybrid Metal Halides: An ab-initio Study of Nonlinear Optical (NLO) Properties

The mixing of organic cations represents yet another direction to explore in the field of chiral organic-inorganic hybrid metal halides (OIHMH). Here, we perform structural optimizations, electronic structures, and non-linear optical (NLO) studies using the density functional theory of two recently synthesized chiral OIHMHs, [R-MePEA][C3A]PbBr4, and [R-MePEA][C4A]PbBr4, with mixed chiral arylammonium and achiral alkylammonium cations. We find that the noncovalent weak interactions (e.g. Br...NH interactions) play an important role in the formation of these OIHMHs. Our study further indicates that the two non-centrosymmetric compounds exhibit relative wide bandgaps (~3.5 eV), strong second harmonic generation (SHG) responses (~0.5-1.5*KDP), and moderate birefringence (~0.088), indicating possible applications NLO materials. Atom response theory analysis reveals that the SHG responses are determined mainly by the occupied Br 3p non-bonding orbitals as well as by the unoccupied Pb 5p orbitals which shows the important contribution of the inorganic PbBr4 layer to the nonlinear optical properties.

cond-mat.mtrl-sci↗

arXiv2018

Interband electron pairing for superconductivity from the breakdown of the Born-Oppenheimer approximation

The origin of interband electron pairing responsible for enhancing superconductivity and the factors controlling its strength were examined. We show that the interband electron pairing is a natural consequence of breaking down the Born-Oppenheimer approximation during the electron-phonon interactions. Its strength is determined by the pair-state excitations around the Fermi surfaces that take place to form a superconducting state. Fermi surfaces favorable for the pairing were found and its implications were discussed.

cond-mat.supr-con↗

arXiv2018

Large second harmonic generation of LiCs2PO4 caused by the metal-cation-centered groups

We evaluated the individual atom contributions to the second harmonic generation (SHG) coefficients of LiCs2PO4 (LCPO) by introducing the partial response functionals on the basis of first principles calculations. The SHG response of LCPO is dominated by the metal-cation-centered groups CsO6 and LiO4, not by the nonmetal-cation-centered groups PO4 one expects from the existing models and theories. The SHG coefficients of LCPO are determined mainly by the occupied orbitals O-2p and Cs-5p as well as by the unoccupied orbitals Cs-5d and Li-2p. For the SHG response of a material, the polarizable atomic orbitals of the occupied and the unoccupied states are both important.

cond-mat.mtrl-sci↗

arXiv2009

Electronic Structure and Lattice dynamics of NaFeAs

The similarity of the electronic structures of NaFeAs and other Fe pnictides has been demonstrated on the basis of first-principle calculations. The global double-degeneracy of electronic bands along X-M and R-A direction indicates the instability of Fe pnictides and is explained on the basis of a tight-binding model. The de Haas-van Alphen parameters for the Fermi surface (FS) of NaFeAs have been calculated. A $\mathbf{Q}_{M}=(1/2,1/2,0)$ spin density wave (SDW) instead of a charge density wave (CDW) ground state is predicted based on the calculated generalized susceptibility $χ(\mathbf{q})$ and a criterion derived from a restricted Hatree-Fock model. The strongest electron-phonon (e-p) coupling has been found to involve only As, Na z-direction vibration with linear-response calculations. A possible enhancement mechanism for e-p coupling due to correlation is suggested.

cond-mat.supr-con↗