Abstract
An observed broad resonance peak in dissociative electron attachment (DEA) cross sections to a molecule might be due to either closely lying or overlapping resonances involved in the process. We developed a state-of-the-art experimental approach that enables us to identify unambiguously both the closely lying and the overlapping resonances based on kinetic energy and/or angular distribution measurements of fragment negative ion(s) generated from DEA process. Experimental observations strongly supported by theoretical potential energy curve calculations unambiguously identify previously unresolved overlapping resonances in DEA to chlorine molecule.
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