التفاصيل البيبلوغرافية
| العنوان: |
H2O2(s) and H2O2·2H2O(s) crystals compared with ices: DFT functional assessment and D3 analysis. |
| المؤلفون: |
Arismendi-Arrieta, Daniel J., Sen, Anik, Eriksson, Anders, Broqvist, Peter, Kullgren, Jolla, Hermansson, Kersti |
| المصدر: |
Journal of Chemical Physics; 11/21/2023, Vol. 159 Issue 19, p1-15, 15p |
| مصطلحات موضوعية: |
DENSITY functionals, FUNCTIONAL assessment, DENSITY functional theory, ICE crystals, FUNCTIONALS, ICE, ENERGY consumption |
| مستخلص: |
The H2O and H2O2 molecules resemble each other in a multitude of ways as has been noted in the literature. Here, we present density functional theory (DFT) calculations for the H2O2(s) and H2O2·2H2O(s) crystals and make selected comparisons with ice polymorphs. The performance of a number of dispersion-corrected density functionals—both self-consistent and a posteriori ones—are assessed, and we give special attention to the D3 correction and its effects. The D3 correction to the lattice energies is large: for H2O2(s) the D3 correction constitutes about 25% of the lattice energy using PBE, much more for RPBE, much less for SCAN, and it primarily arises from non-H-bonded interactions out to about 5 Å.The large D3 corrections to the lattice energies are likely a consequence of several effects: correction for missing dispersion interaction, the ability of D3 to capture and correct various other kinds of limitations built into the underlying DFT functionals, and finally some degree of cell-contraction-induced polarization enhancement. We find that the overall best-performing functionals of the twelve examined are optPBEvdW and RPBE-D3. Comparisons with DFT assessments for ices in the literature show that where the same methods have been used, the assessments largely agree. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |