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Shilie Pan

Publications and source records attributed to Shilie Pan.

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Impact of scissors-correction schemes on first-principles calculations of second-harmonic generation in ultraviolet nonlinear-optical crystals

In this work, we assess two widely used scissors-correction schemes for first-principles calculations of second-harmonic generation in representative borate and phosphate ultraviolet nonlinear-optical (UV-NLO) crystals, namely scheme-L [Phys.\ Rev.\ Lett.\ \textbf{63}, 1719 (1989)] and scheme-N [Phys.\ Rev.\ B \textbf{72}, 045223 (2005)]. To enable controlled and numerically robust comparisons, we derive a unified static-limit formulation that avoids spurious divergences and is applicable to both schemes, thereby extending earlier static-limit treatments that were effectively restricted to scheme-L. Benchmark calculations show that both schemes largely preserve the spectral line shape while mainly rescaling the overall response. Scheme-N systematically yields 15\%--25\% larger SHG magnitudes than scheme-L, although for some tensor components and experimental datasets scheme-L shows closer agreement with experiment. We further show that Kleinman symmetry is satisfied in the static limit at the level of the formal theory, whereas apparent violations in practical calculations arise mainly from the numerical approximation used to evaluate generalized derivatives.

physics.chem-ph

Origin of second harmonic generation in non-centrosymmetric crystal structures containing lone-pairs electrons

Material systems with lone-pair electrons have long been a treasure trove in the search for large second harmonic generation effects. Revealing the origin of second harmonic generation in nonlinear optical materials can provide theoretical guidance for the design of new materials. In this work, the origin of second harmonic generation in non-centrosymmetric materials containing lone pair electrons is revealed by analyzing the orbital interactions on the sublattice. Stereochemically inactive Pb 6\textit{s} orbitals with high symmetry in CsPbCO3F contribute less to the second harmonic generation. In contrast, the contribution of stereochemically active Pb 6s orbital in PbB5O7F3 and PbB2O3F2 is more obvious. Significantly, the orbitals of the interaction between lead and oxygen make a very significant contribution because these orbitals are located at the band edge and in non-centrosymmetric sublattices.

cond-mat.mtrl-sci

A full breakthrough in vacuum ultraviolet nonlinear optical performance of NH4B4O6F

The lack of suitable vacuum ultraviolet (VUV) nonlinear optical (NLO) crystals has hindered the development of compact, high-power VUV sources via second harmonic generation (SHG). Here, we report on the development of the fluorooxoborate crystal NH4B4O6F (ABF) as a promising material for VUV light generation. For the first time, devices with specific phase-matching angles were constructed, achieving a record 158.9 nm VUV light through phase-matching SHG and a maximum nanosecond pulse energy of 4.8 mJ at 177.3 nm with a conversion efficiency of 5.9 %. The enhanced NLO performance is attributed to optimized arrangements of fluorine-based units creating asymmetric sublattices. This work marks a significant milestone in the field of NLO materials, facilitating the future applications of compact, high-power VUV lasers utilizing ABF.

cond-mat.mtrl-sci

A family of air-stable chalcogenide solid electrolytes in Li$_2$BMQ$_4$ (B = Ca, Sr and Ba; M = Si, Ge and Sn; Q = O, S and Se) systems

Combining high-throughput first-principles calculations and experimental measurements, we have identified a novel family of fast lithium-ion chalcogenide conductors in Li$_2$BMQ$_4$ (2114, B = Ca, Sr and Ba; M = Si, Ge and Sn; Q = O, S and Se) systems. Our calculations demonstrate that most of the thermodynamically and kinetically stable sulfides and selenides in this new system exhibit ultralow Li$^+$ ion migration activation energy (0.16 eV ~ 0.56 eV) and considerable bandgaps varying between ~ 2 eV and 3.5 eV. We have successfully synthesized Li$_2$BaSnS$_4$ and Li$_2$SrSiS$_4$, and they exhibit excellent moisture stability through H$_2$S gas measurements. Electrochemical impedance measurements indicate 2114 systems show the typical features of solid ionic conductors, with a room-temperature Li$^+$ conductivity close to 5$\times$10$^{-4}$ mS/cm aligning with our molecular dynamics simulations. Furthermore, we have theoretically investigated the substitution of Cl$^-$ at S$^{2-}$ site. The doped compounds display significantly higher conductivity, with an increase of about three orders of magnitude (up to a maximum of 0.72 mS/cm) compared to the undoped compounds. These findings offer valuable insights for the further exploration of potential chalcogenide solid electrolyte materials with robust air stability and enhanced ionic conductivity for practical applications in lithium-ion batteries.

cond-mat.mtrl-sci

Prediction of Ternary Fluorooxoborates with Coplanar Triangle Units [BOxF3-x]x- From First-Principles

Ten new ternary fluorooxoborate structures were obtained from first-principles prediction. Coplanar aligned triangle structure units [BO2F]2- and [BOF2]- like [BO3]3- in borates were found from the computational simulation. We identified new covalent coordination patterns of the F atom connected with the B atoms which are located in the bridging site, -B--F--B-. Besides, one molecular crystal with [B4O4F4] molecular unit was attached.

cond-mat.mtrl-sci