1. Thermal expansion in dispersion-bound molecular crystals
- Author
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Hsin-Yu Ko, Robert A. DiStasio, Biswajit Santra, and Roberto Car
- Subjects
Condensed Matter - Materials Science ,Materials science ,Physics and Astronomy (miscellaneous) ,Condensed matter physics ,Intermolecular force ,Anharmonicity ,Materials Science (cond-mat.mtrl-sci) ,FOS: Physical sciences ,02 engineering and technology ,021001 nanoscience & nanotechnology ,01 natural sciences ,Thermal expansion ,symbols.namesake ,Pauli exclusion principle ,0103 physical sciences ,Dispersion (optics) ,symbols ,Melting point ,General Materials Science ,010306 general physics ,0210 nano-technology ,Debye model ,Quantum fluctuation - Abstract
We explore how anharmonicity, nuclear quantum effects (NQE), many-body dispersion interactions, and Pauli repulsion influence thermal properties of dispersion-bound molecular crystals. Accounting for anharmonicity with ab initio molecular dynamics yields cell parameters accurate to within $2%$ of experiment for a set of pyridinelike molecular crystals at finite temperatures and pressures. From the experimental thermal expansion curve, we find that pyridine-I has a Debye temperature just above its melting point, indicating sizable NQE across the entire crystalline range of stability. We find that NQE lead to a substantial volume increase in pyridine-I $(\ensuremath{\approx}40$% more than classical thermal expansion at 153 K) and attribute this to intermolecular Pauli repulsion promoted by intramolecular quantum fluctuations. When predicting delicate properties such as the thermal expansivity, we show that many-body dispersion interactions and more sophisticated density functional approximations improve the accuracy of the theoretical model.
- Published
- 2018
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