Time-resolved photoelectron diffraction imaging of methanol photodissociation involving molecular hydrogen ejection.
Kazuki YoshikawaManabu KannoHao XueNaoki KishimotoSoki GotoFukiko OtaYoshiaki TamuraFlorian TrinterKilian FehreLeon KaiserJonathan StindlDimitrios TsitsonisMarkus S SchöfflerReinhard DörnerRebecca BollBenjamin ErkTommaso MazzaTerence MullinsDaniel E RivasPhilipp SchmidtSergey UsenkoMichael MeyerEnliang WangDaniel RollesArtem RudenkoEdwin KukkTill JahnkeSergio Diaz-TenderoFernando MartinKeisuke HatadaKiyoshi UedaPublished in: Physical chemistry chemical physics : PCCP (2024)
Imaging ultrafast atomic and molecular hydrogen motion with femtosecond time resolution is a challenge for ultrafast spectroscopy due to the low mass and small scattering cross section of the moving neutral hydrogen atoms and molecules. Here, we propose time- and momentum-resolved photoelectron diffraction (TMR-PED) as a way to overcome limitations of existing methodologies and illustrate its performance using a prototype molecular dissociation process involving the sequential ejection of a neutral hydrogen molecule and a proton from the methanol dication. By combining state-of-the-art molecular dynamics and electron-scattering methods, we show that TMR-PED allows for direct imaging of hydrogen atoms in action. More specifically, the fingerprint of hydrogen dynamics reflects the time evolution of polarization-averaged molecular-frame photoelectron angular distributions (PA-MFPADs) as would be recorded in X-ray pump/X-ray probe experiments with few-femtosecond resolution. We present the results of two precursor experiments that support the feasibility of this approach.