Sun Jiuyu, Lee Cheng-Wei, Kononov Alina, Schleife André, Ullrich Carsten A
Department of Physics and Astronomy, University of Missouri, Columbia, Missouri 65211, USA.
Max Planck Institute for the Structure and Dynamics of Matter, 22761 Hamburg, Germany.
Phys Rev Lett. 2021 Aug 13;127(7):077401. doi: 10.1103/PhysRevLett.127.077401.
Linear-response time-dependent density-functional theory (TDDFT) can describe excitonic features in the optical spectra of insulators and semiconductors, using exchange-correlation (xc) kernels behaving as -1/k^{2} to leading order. We show how excitons can be modeled in real-time TDDFT, using an xc vector potential constructed from approximate, long-range corrected xc kernels. We demonstrate, for various materials, that this real-time approach is consistent with frequency-dependent linear response, gives access to femtosecond exciton dynamics following short-pulse excitations, and can be extended with some caution into the nonlinear regime.
线性响应含时密度泛函理论(TDDFT)能够利用在主导阶表现为-1/k² 的交换关联(xc)核来描述绝缘体和半导体光谱中的激子特性。我们展示了如何在实时TDDFT中对激子进行建模,即使用由近似的、长程校正的xc核构建的xc矢量势。我们针对各种材料证明,这种实时方法与频率相关的线性响应一致,能够获取短脉冲激发后的飞秒激子动力学,并且可以谨慎地扩展到非线性 regime。