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学術論文

Direct tracking of ultrafast proton transfer in water dimers

MPS-Authors
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Schnorr,  Kirsten       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Augustin,  Sven       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Lindenblatt,  Hannes       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Liu,  Yifan
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Meister,  Severin       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Pfeifer,  Thomas       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Schmid,  Georg
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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Moshammer,  Robert       
Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society;

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引用

Schnorr, K., Belina, M., Augustin, S., Lindenblatt, H., Liu, Y., Meister, S., Pfeifer, T., Schmid, G., Treusch, R., Trost, F., Slavilek, P., & Moshammer, R. (2023). Direct tracking of ultrafast proton transfer in water dimers. Science Advances, 9(28):. doi:10.1126/sciadv.adg7864.


引用: https://hdl.handle.net/21.11116/0000-000D-CCF9-5
要旨
Upon ionization, water forms a highly acidic radical cation H2O+· that undergoes ultrafast proton transfer (PT)—a pivotal step in water radiation chemistry, initiating the production of reactive H3O+, OH radicals, and a (hydrated) electron. Until recently, the time scales, mechanisms, and state-dependent reactivity of ultrafast PT could not be directly traced. Here, we investigate PT in water dimers using time-resolved ion coincidence spectroscopy applying a free-electron laser. An extreme ultraviolet (XUV) pump photon initiates PT, and only dimers that have undergone PT at the instance of the ionizing XUV probe photon result in distinct H3O+ + OH+ pairs. By tracking the delay-dependent yield and kinetic energy release of these ion pairs, we measure a PT time of (55 ± 20) femtoseconds and image the geometrical rearrangement of the dimer cations during and after PT. Our direct measurement shows good agreement with nonadiabatic dynamics simulations for the initial PT and allows us to benchmark nonadiabatic theory.