Abstract

AbstractThe Auger spectrum of solid hydrogen fluoride is calculated by an ab initio Green's function method. Already small clusters lead to saturation with respect to cluster size. The differences which arise when going from the gas to the solid phase Auger spectrum are mainly a broadening of the lines and the emergence of an additional feature at high kinetic energies. This additional feature is assigned to transitions to delocalized final states.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call