离子键合
离子势
凝聚态物理
偶极子
再分配(选举)
从头算
化学
电偶极矩
基本电荷
张量(固有定义)
电荷(物理)
有效核电荷
拉曼光谱
物理
离子
电子
光学
量子力学
有机化学
政治
法学
纯数学
数学
政治学
作者
E. Burstein,M. H. Brodsky,G. Lucovsky
标识
DOI:10.1002/qua.560010682
摘要
The ionic charges of zincblende type crystals are discussed. Since the static ionic charges are, in general, quite small in these crystals, the magnitudes of the dynamic ionic charge, e*T, are attributed largely to the effects of charge redistribution. The fairly sizeable values of e*T in Se and Te trigonal crystals must, in fact, be attributed entirely to charge redistribution effects since their static ionic charges are identically zero. Efforts to account for the e*T values in ZnS type crystals using either the shell model or the deformation dipole model have not been too successful. It is urged that theorists turn their attention to ab initio energy-band calculations of long wavelength dynamical properties of zincblende and diamond type crystals, namely: the first-order electric moment (infrared) tensor, ∂M/∂uT; the first-order electric susceptibility (Raman) tensor, ∂χ0/∂uT; and the change in the electric susceptibility with interatomic distance (piezo-optic) tensor, ∂χ0/∂∂.
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