Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba 305-8571, Japan.
J Chem Phys. 2011 Apr 14;134(14):144106. doi: 10.1063/1.3575587.
We apply the adiabatic time-dependent density functional theory to magnetic circular dichroism (MCD) spectra using the real-space, real-time computational method. The standard formulas for the MCD response and its A and B terms are derived from the observables in the time-dependent wave function. We find real-time method is well suited for calculating the overall spectrum, particularly at higher excitation energies where individual excited states are numerous and overlapping. The MCD sum rules are derived and intepreted in the real-time formalism; we find that they are very useful for normalization purposes and assessing the accuracy of the theory. The method is applied to MCD spectrum of C(60) using the adiabatic energy functional from the local density approximation. The theory correctly predicts the signs of the A and B terms for the lowest allowed excitations. However, the magnitudes of the terms only show qualitative agreement with experiment.
我们应用绝热含时密度泛函理论,采用实空间、实时计算方法,对磁圆二色性(MCD)光谱进行了研究。从含时波函数中的可观测量出发,推导出了 MCD 响应及其 A 和 B 项的标准公式。我们发现,实时方法非常适合计算整体光谱,特别是在激发能较高的情况下,此时存在大量重叠的单个激发态。在实时形式中推导出了 MCD 总和规则,并对其进行了解释;我们发现,它们对于归一化目的和评估理论的准确性非常有用。我们使用局域密度近似的绝热能量泛函,将该方法应用于 C(60)的 MCD 光谱。该理论正确预测了最低允许激发的 A 和 B 项的符号。然而,这些项的幅度仅与实验定性一致。