Communication: Non-additivity of van der Waals interactions between nanostructures

被引:24
|
作者
Tao, Jianmin [1 ]
Perdew, John P. [2 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[2] Temple Univ, Dept Phys, Philadelphia, PA 19122 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 141卷 / 14期
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; DISPERSION COEFFICIENTS; LONDON; POLARIZABILITIES; FULLERENES;
D O I
10.1063/1.4897957
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Due to size-dependent non-additivity, the van der Waals interaction (vdW) between nanostructures remains elusive. Here we first develop a model dynamic multipole polarizability for an inhomogeneous system that allows for a cavity. The model recovers the exact zero- and high-frequency limits and respects the paradigms of condensed matter physics (slowly varying density) and quantum chemistry (one- and two-electron densities). We find that the model can generate accurate vdW coefficients for both spherical and non-spherical clusters, with an overall mean absolute relative error of 4%, without any fitting. Based on this model, we study the non-additivity of vdW interactions. We find that there is strong non-additivity of vdW interactions between nanostructures, arising from electron delocalization, inequivalent contributions of atoms, and non-additive many-body interactions. Furthermore, we find that the non-additivity can have increasing size dependence as well as decreasing size dependence with cluster size. (C) 2014 AIP Publishing LLC.
引用
收藏
页数:4
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