Vibrational-resolved ion and ion-pair yield spectra of N-2 and CO taken at
their 1s --> pi* resonance excitations reveal decay-channel-dependent core
hole lifetimes. The linewidths of the yield spectra tend to be shortened wh
en the number of electrons ejected in the deexcitation process increases, f
inally becoming narrower than the total ion yield or absorption natural lif
etime width of the core-excited states of N-2 and CO, respectively. In cont
rast to this, the linewidths of the yield spectra for the singly charged mo
lecular ions, N-2(+) and CO+, are shown to be broader than their correspond
ing natural linewidths. This linewidth shortening and broadening observed i
n the ion yield spectra are explained by the effect of different internucle
ar distances on the lifetime of an excited molecular state.