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Molecular dynamics simulations of some amorphous and crystalline photonic materials

Published online by Cambridge University Press:  31 January 2011

Pradeep P. Phule
Affiliation:
Department of Materials Science and Engineering, University of Arizona, Tucson, Arizona 85721
Pierre A. Deymier
Affiliation:
Department of Materials Science and Engineering, University of Arizona, Tucson, Arizona 85721
Subhash H. Risbud
Affiliation:
Department of Materials Science and Engineering, University of Arizona, Tucson, Arizona 85721
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Abstract

Constant pressure molecular dynamics (MD) simulations have been used to simulate amorphous and crystalline forms of BaTiO3 and TiO2. Simulation results for pure RaTiO3 and TiO2 glasses show fourfold titanium coordination with a Ti–O bond distance of 1.8 Å, consistent with experimental evidence for the structure of titania doped glasses for all optical switching and ultra low expansivity (ULE) TiO2–SiO2 glasses. Radial distribution function data for crystalline, liquid, and amorphous forms of BaTiO3 were also obtained. The displacement polarization and its contribution to susceptibilities have been calculated by application of an electric field to the simulation cell. The calculated ionic dielectric constants (Ki) for simulated NaCI (crystal), TiO2 glass, and TiO2 (crystal) were 3.34, 5.96, and 19.4 as compared to the experimental values of ≍3.34, 3–10, and 78, respectively. The calculated cubic nonlinear susceptibility (ξ3) values for NaCI (crystal), TiO2 (glass), and TiO2 (crystal) were, respectively, 0.194, 2.175, and 4.68 (x 10−18m2V−2). The increase in ξ3 values is consistent with experimentally observed trends of the linear refractive indices. Improved agreement between experimental and calculated values of susceptibilities and dielectric constant was obtained for materials with higher ionicity.

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Articles
Copyright
Copyright © Materials Research Society 1990

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References

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