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发布时间：2019-03-10

论文类型：期刊论文

发表时间：2017-05-03

发表刊物：2nd Molecular Simulation Conference

收录刊物：CPCI-S、EI、SCIE

卷号：43

期号：7

页面范围：568-574

ISSN号：0892-7022

关键字：Energetic materials; dispersion correction; lattice energy; bulk modulus; assessment

摘要：Accurate description of the non-covalent intermolecular interaction is significant for the study of energetic materials. Here, the performance of a variety of dispersion correction methods within density functional theory (DFT) is assessed carefully for six energetic molecular crystals using experimental data as benchmark. We consider semi-empirical DFT plus dispersion correction methods (DFT-D, including DFT-D2 and DFT-D3) and non-empirical van der Waals density functional correction methods (including vdW-DF, vdW-DF2, optPBE-vdW, optB88-vdW and optB86b-vdW). The calculative cell volume, lattice energies, pressure-induced change of volume and bulk modulus are compared with the available experimental data. At ambient condition, theoretical cell volumes by optPBE-vdW, PBE-D3 and vdW-DF2 are in reasonable accordance with experimental data, while PBE-D3 and vdW-DF2 give satisfactory for lattice energies. Under high pressure, both semi-empirical PBE-D3 and non-empirical vdW-DF2 methods could yield reliable results, in which the results by PBE-D3 have smaller deviation from experiment than vdW-DF2 in the entire pressure range. Furthermore, bulk modulus by PBE-D3 calculations also compares reasonably with experimental data. These present assessments provide valuable guidelines for selecting the appropriate method to investigate physical and chemical proprieties of energetic materials in the future.