“…Also in these cases we recorded negative energy shifts having a bigger value, indicating a more attractive behavior in the case of He * -M collisions respect to Ne * -M collisions (with M = H2S, NH3). This observation is in fairly good agreement with previous results obtained by Ohno et al [27] and Ben Arfa et al [39] P2 state), which is the fundamental physical property of the partners, enhancing the attractive interaction behavior of the potential energy surfaces [22]. As already discussed in previous papers [22,23], by a simple analysis of obtained PIES spectra, in the case of H2O + -1b1, H2S + -2b1, and NH3 + shift, εmax, from the change in position of the maximum of peak but also the shift between the electron energy value where the peak intensity drops down to 44% of its maximum at the lower energy side, εA, with respect to the nominal energy, ε0 [40].…”