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arXiv 1007.3305cond-mat.mtrl-sci
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分子晶体中束缚的范德华密度泛函计算

van der Waals density functional calculations of binding in molecular crystals

Kristian Berland, Oyvind Borck, Per Hyldgaard

摘要:

最近的论文[J.Chem.Phys.132,134705(2010)]说明了范德华密度泛函(vdW-DF)方法的潜力[Phys.Rev.Lett. 92,246401(2004)]用于分子晶体中结构和内聚的有效第一原理解释。从那时起,已经提出了对原始vdW-DF版本(标识为vdW-DF 1)的修改,并且在vdW-DF框架内还有一个称为vdW-DF 2的新版本[ArXiv 1003.5255]。在这里,我们调查的性能和性质的修改和一组简单的分子晶体的绑定的新版本:六胺,dodecahedrane,C60,和石墨。这些扩展的系统提供了处理稀疏物质的计算方法的基准。我们发现,以前记录的增强vdw-DF 1的非本地相关性的渐近原子为基础的帐户接近和几个A,超越绑定分离持续在vdw-DF 2。计算和分析分子晶体中的结合需要适当的计算工具。在本文中,我们还介绍了我们的vdw-DF相关的实空间并行实现的细节和用于生成渐近原子为基础的对电位的基础上vdw-DF的方法。

英文摘要:

A recent paper [J. Chem. Phys. 132, 134705 (2010)] illustrated the potential of the van der Waals density functional (vdW-DF) method [Phys. Rev. Lett. 92, 246401 (2004)] for efficient first-principle accounts of structure and cohesion in molecular crystals. Since then, modifications of the original vdW-DF version (identified as vdW-DF1) has been proposed, and there is also a new version called vdW-DF2 [ArXiv 1003.5255], within the vdW-DF framework. Here we investigate the performance and nature of the modifications and the new version for the binding of a set of simple molecular crystals: hexamine, dodecahedrane, C60, and graphite. These extended systems provide benchmarks for computational methods dealing with sparse matter. We show that a previously documented enhancement of non-local correlations of vdW-DF1 over an asymptotic atom-based account close to and a few A, beyond binding separation persists in vdW-DF2. The calculation and analysis of the binding in molecular crystals requires appropriate computational tools. In this paper, we also present details on our real-space parallel implementation of the vdW-DF correlation and on the method used to generate asymptotic atom-based pair potentials based on vdW-DF.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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