Abstract

We present a new complex-scaling Fourier-grid Hamiltonian (CSFGH) method for accurate and efficient determination of laser-induced (multichannel) molecular resonance states without the use of basis set expansions. The method requires neither the computation of potential matrix elements nor the imposition of boundary conditions, and the eigenvectors provide directly the values of the resonance wave functions at the space grid points. The procedure is particularly valuable for excited-state problems where basis set expansion methods face the challenge. The simplicity and usefulness of the CSFGH method is demonstrated by a case study of the intensity-dependent complex quasivibrational energy eigenvalues (ER, −Γ/2) and eigenvectors associated with multiphoton and above-threshold dissociation of H+2 ions in the presence of intense laser fields (I=1012–1014 W/cm2 ).

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