Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/145066
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dc.contributor.authorKjellsson, L.en_US
dc.contributor.authorNanda, K. D.en_US
dc.contributor.authorRubensson, J.-E.en_US
dc.contributor.authorDoumy, G.en_US
dc.contributor.authorSouthworth, S. H.en_US
dc.contributor.authorHo, P. J.en_US
dc.contributor.authorMarch, A. M.en_US
dc.contributor.authorAl Haddad, A.en_US
dc.contributor.authorKumagai, Y.en_US
dc.contributor.authorTu, M.-F.en_US
dc.contributor.authorSchaller, R. D.en_US
dc.contributor.authorDebnath, Tusharen_US
dc.contributor.authorMuhamamd Shafiq Mohd Yusofen_US
dc.contributor.authorArnold, C.en_US
dc.contributor.authorSchlotter, W. F.en_US
dc.contributor.authorMoeller, S.en_US
dc.contributor.authorCoslovich, G.en_US
dc.contributor.authorKoralek, J. D.en_US
dc.contributor.authorMinitti, M. P.en_US
dc.contributor.authorVidal, M. L.en_US
dc.contributor.authorSimon, M.en_US
dc.contributor.authorSantra, R.en_US
dc.contributor.authorLoh, Zhi-Hengen_US
dc.contributor.authorCoriani, S.en_US
dc.contributor.authorKrylov, A. I.en_US
dc.contributor.authorYoung, L.en_US
dc.date.accessioned2020-12-10T01:46:27Z-
dc.date.available2020-12-10T01:46:27Z-
dc.date.issued2020-
dc.identifier.citationKjellsson, L., Nanda, K. D., Rubensson, J.-E., Doumy, G., Southworth, S. H., Ho, P. J., . . . Young, L. (2020). Resonant inelastic x-ray scattering reveals hidden local transitions of the aqueous OH radical. Physical Review Letters, 124(23), 236001-. doi:10.1103/PhysRevLett.124.236001en_US
dc.identifier.issn0031-9007en_US
dc.identifier.urihttps://hdl.handle.net/10356/145066-
dc.description.abstractResonant inelastic x-ray scattering (RIXS) provides remarkable opportunities to interrogate ultrafast dynamics in liquids. Here we use RIXS to study the fundamentally and practically important hydroxyl radical in liquid water, OH(aq). Impulsive ionization of pure liquid water produced a short-lived population of OH(aq), which was probed using femtosecond x-rays from an x-ray free-electron laser. We find that RIXS reveals localized electronic transitions that are masked in the ultraviolet absorption spectrum by strong charge-transfer transitions-thus providing a means to investigate the evolving electronic structure and reactivity of the hydroxyl radical in aqueous and heterogeneous environments. First-principles calculations provide interpretation of the main spectral features.en_US
dc.description.sponsorshipMinistry of Education (MOE)en_US
dc.language.isoenen_US
dc.relationMOE2014-T2-2-052en_US
dc.relationRG105/17en_US
dc.relationRG109/18en_US
dc.relation.ispartofPhysical Review Lettersen_US
dc.rights© 2020 American Physical Society. All rights reserved. This paper was published in Physical Review Letters and is made available with permission of American Physical Society.en_US
dc.subjectPhysics - Chemical Physicsen_US
dc.subjectPhysics - Chemical Physicsen_US
dc.subjectScience::Physicsen_US
dc.titleResonant inelastic x-ray scattering reveals hidden local transitions of the aqueous OH radicalen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1103/PhysRevLett.124.236001-
dc.description.versionPublished versionen_US
dc.identifier.pmid32603165-
dc.identifier.issue23en_US
dc.identifier.volume124en_US
dc.subject.keywordsX-rayen_US
dc.subject.keywordsHydroxyl Radicalen_US
dc.description.acknowledgementThis work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Science, Chemical Sciences, Geosciences and Biosciences Division that supported the Argonne group under Contract No. DE-AC02- 06CH11357. Use of the Linac Coherent Light Source (LCLS), SLAC National Accelerator Laboratory, and resources of the Center for Nanoscale Materials (CNM), Argonne National Laboratory, are supported by the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES) under Contracts No. DEAC02-76SF00515 and No. DE-AC02-06CH11357. L. Y. acknowledges support from Laboratory Directed Research and Development (LDRD) funding from Argonne National Laboratory for conceptual design and proposal preparation. L. K., J.-E. R. acknowledge support from the Swedish Science Council (Grant No. 2018-04088). L. K. was also supported by the European X-ray Free Electron Laser. Z.-H. L., T. D., and M. S. B. M. Y. acknowledge support from the Singapore Ministry of Education (MOE2014-T2-2- 052, RG105/17, and RG109/18). M. S. was supported by the CNRS GotoXFEL program. C. A. and R. S. were supported by the Cluster of Excellence “Advanced Imaging of Matter” of the Deutsche Forschungsgemeinschaft (DFG)—EXC 2056—Project ID No. 390715994. R. S. acknowledges support by the Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy, Grant No. DE-SC0019451. M. L. V. and S. C. acknowledge support from DTU Chemistry (start-up PhD grant). S. C. acknowledges support from the Independent Research Fund Denmark DFF-RP2 Grant No. 7014-00258B. At USC, this work was supported by the U.S. National Science Foundation (Grant No. CHE-1856342 to A. I. K.). A. I. K. is also a grateful recipient of the Simons Fellowship in Theoretical Physics and Mildred Dresselhaus Award from the Hamburg Centre for Ultrafast Imaging, which supported her sabbatical stay in Germany.en_US
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