Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentation
Michael Gatchell, Mark H. Stockett, Nathalie de Ruette, Tao Chen,, Linda Giacomozzi, Rodrigo F. Nascimento, Michael Wolf, Emma K. Anderson, Rudy, Delaunay, Violaine Viziano, Patrick Rousseau, Lamri Adoui, Bernd A. Huber,, Henning T. Schmidt, Henning Zettergren, Henrik Cederquist

TL;DR
This study challenges previous claims by showing that hydrogenation does not protect polycyclic aromatic hydrocarbons from fragmentation; instead, it increases the likelihood of backbone fragmentation during collisions.
Contribution
The paper provides experimental evidence that hydrogenation does not shield PAHs from fragmentation, contradicting earlier findings based on soft X-ray absorption studies.
Findings
Hydrogenation increases backbone fragmentation cross section.
Experimental results oppose previous protection hypothesis.
Fragmentation likelihood rises with hydrogenation degree.
Abstract
A recent study of soft X-ray absorption in native and hydrogenated coronene cations, CH , led to the conclusion that additional hydrogen atoms protect (interstellar) Polycyclic Aromatic Hydrocarbon (PAH) molecules from fragmentation [Reitsma et al., Phys. Rev. Lett. 113, 053002 (2014)]. The present experiment with collisions between fast (30-200 eV) He atoms and pyrene (CH, , 6, and 16) and simulations without reference to the excitation method suggests the opposite. We find that the absolute carbon-backbone fragmentation cross section does not decrease but increases with the degree of hydrogenation for pyrene molecules.
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