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Investigating charge-up and fragmentation dynamics of oxygen molecules after interaction with strong X-ray free-electron laser pulses.

G KastirkeF OtaD V RezvanMarkus S SchöfflerM WellerJonas RistRebecca BollN AndersT M BaumannSebastian EckartBenjamin ErkA De FanisK FehreA GattonSven GrundmannPatrik GrychtolA HartungM HofmannM IlchenC JankeM KircherM KunitskiX LiT MazzaNiklas MelzerJ MontanoV MusicGiammarco NalinY OvcharenkoA PierN RennhackD E RivasR DörnerDaniel RollesA RudenkoPhilipp SchmidtJ SiebertN StrengerD TrabertI Vela-PerezR WagnerThorsten WeberJ B WilliamsP ZiolkowskiL Ph H SchmidtA CzaschY TamuraN HaraKaoru YamazakiK HatadaFlorian TrinterM MeyerK UedaPhilipp V DemekhinTill Jahnke
Published in: Physical chemistry chemical physics : PCCP (2022)
During the last decade, X-ray free-electron lasers (XFELs) have enabled the study of light-matter interaction under extreme conditions. Atoms which are subject to XFEL radiation are charged by a complex interplay of (several subsequent) photoionization events and electronic decay processes within a few femtoseconds. The interaction with molecules is even more intriguing, since intricate nuclear dynamics occur as the molecules start to dissociate during the charge-up process. Here, we demonstrate that by analyzing photoelectron angular emission distributions and kinetic energy release of charge states of ionic molecular fragments, we can obtain a detailed understanding of the charge-up and fragmentation dynamics. Our novel approach allows for gathering such information without the need of complex ab initio modeling. As an example, we provide a detailed view on the processes happening on a femtosecond time scale in oxygen molecules exposed to intense XFEL pulses.
Keyphrases
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  • single molecule