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Issue 22, 2009
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Towards a gauge invariant method for molecular chiroptical properties in TDDFT

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Abstract

We present an efficient scheme to calculate the chiroptical response of molecular systems within time dependent density functional theory using either a real-time propagation or a frequency-dependent Sternheimer method. The scheme avoids the commonly used sum over empty orbitals and has a very favorable scaling with system size. Moreover, the method is general and can be easily implemented. In the present work, we implemented it using a real-space pseudo-potential representation of the wave-functions and Hamiltonian. The specific use of non-local pseudo-potentials implies that a gauge correction term in the angular momentum operator must be included to ensure that the total scheme is fully gauge invariant. Applications to small organic chiral molecules are shown and discussed, addressing some deficiencies of present exchange–correlation functionals to describe the absolute position of the excitations. However, the shape or sign of the dichroism spectra comes out in excellent agreement with available experiments.

Graphical abstract: Towards a gauge invariant method for molecular chiroptical properties in TDDFT

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Publication details

The article was received on 16 Feb 2009, accepted on 17 Mar 2009 and first published on 14 Apr 2009


Article type: Paper
DOI: 10.1039/B903200B
Citation: Phys. Chem. Chem. Phys., 2009,11, 4481-4489
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    Towards a gauge invariant method for molecular chiroptical properties in TDDFT

    D. Varsano, L. A. Espinosa-Leal, X. Andrade, M. A. L. Marques, R. di Felice and A. Rubio, Phys. Chem. Chem. Phys., 2009, 11, 4481
    DOI: 10.1039/B903200B

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