Abbreviated Journal Title
J. Chem. Phys.
QUANTUM-DEFECT THEORY; DOUBLE-RESONANCE SPECTROSCOPY; HIGH RYDBERG; STATES; ELECTRON-ION RECOMBINATION; VIBRATIONAL AUTOIONIZATION; TEMPERATURE-DEPENDENCE; AB-INITIO; IONIZATION; COEFFICIENTS; EXCITATION; Physics, Atomic, Molecular & Chemical
We present a theoretical study of the indirect dissociative recombination of linear polyatomic ions at low collisional energies. The approach is based on the computation of the scattering matrix just above the ionization threshold and enables the explicit determination of all diabatic electronic couplings responsible for dissociative recombination. In addition, we use the multi-channel quantum-defect theory to demonstrate the precision of the scattering matrix by reproducing accurately ab initio Rydberg state energies of the neutral molecule. We consider the molecular ions N2H+ and HCO+ as benchmark systems of astrophysical interest and improve former theoretical studies, which had repeatedly produced smaller cross sections than experimentally measured. Specifically, we demonstrate the crucial role of the previously overlooked stretching modes for linear polyatomic ions with large permanent dipole moment. The theoretical cross sections for both ions agree well with experimental data over a wide energy range. Finally, we consider the potential role of the HOC+ isomer in the experimental cross sections of HCO+ at energies below 10 meV.
Journal of Chemical Physics
Fonseca dos Santos, S.; Douguet, N.; Kokoouline, V.; and Orel, A E., "Scattering matrix approach to the dissociative recombination of HCO+ and N2H+" (2014). Faculty Bibliography 2010s. 5267.