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  1. AU="Bozek, John D"
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  1. Article ; Online: Resonant Auger decay of dissociating CH3I near the I 4d threshold.

    Pratt, Stephen T / Jacovella, Ugo / Gans, Bérenger / Bozek, John D / Holland, David M P

    The Journal of chemical physics

    2024  Volume 160, Issue 7

    Abstract: Resonant Auger processes provide a unique perspective on electronic interactions and excited vibrational and electronic states of molecular ions. Here, new data are presented on the resonant Auger decay of excited CH3I in the region just below the I 4d-1 ...

    Abstract Resonant Auger processes provide a unique perspective on electronic interactions and excited vibrational and electronic states of molecular ions. Here, new data are presented on the resonant Auger decay of excited CH3I in the region just below the I 4d-1 ionization threshold. The resonances include the Rydberg series converging to the five spin-orbit and ligand-field split CH3I (I 4d-1) thresholds, as well as resonances corresponding to excitation from the I 4d5/2,3/2 orbitals into the σ* lowest unoccupied molecular orbital. This study focuses on participator decay that populates the lowest lying states of CH3I+, in particular, the X̃2E3/2 and 2E1/2 states, and on spectator decay that populates the lowest-lying (CH3I2+)σ* states of CH3I+. The CH3I (I 4d-1)σ* resonances are broad, and dissociation to CH3 + I competes with the autoionization of the core-excited states. Auger decay as the molecule dissociates produces a photoelectron spectrum with a long progression (up to v3+ ∼ 25) in the C-I stretching mode of the X̃2E3/2 and 2E1/2 states, providing insights into the shape of the dissociative core-excited surface. The observed spectator decay processes indicate that CH3I+ is formed on the repulsive wall of the lower-lying (CH3I2+)σ* potentials, and the photon-energy dependence of the processes provides insights into the relative slopes of the (4d-1)σ* and (CH3I2+)σ* potential surfaces. Data are also presented for the spectator decay of higher lying CH3I (I 4d-1)nl Rydberg resonances. Photoelectron angular distributions for the resonant Auger processes provide additional information that helps distinguish these processes from the direct ionization signal.
    Language English
    Publishing date 2024-02-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/5.0190794
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Resonant Auger decay of iodobenzene below the I 4d edge.

    Pratt, Stephen T / Jacovella, Ugo / Gans, Bérenger / Bozek, John D / Holland, David M P

    The Journal of chemical physics

    2024  Volume 160, Issue 17

    Abstract: New data are presented on the resonant Auger decay of iodobenzene (C6H5I) in the region of the I 4d-1 ionization threshold. The excited molecules decay by participator and spectator processes to populate single-hole valence states and two-hole, one- ... ...

    Abstract New data are presented on the resonant Auger decay of iodobenzene (C6H5I) in the region of the I 4d-1 ionization threshold. The excited molecules decay by participator and spectator processes to populate single-hole valence states and two-hole, one-particle excited states of the cation, providing new information on the structure of C6H5I+. Excitation of dissociative C6H5I (I 4d5/2,3/2-1)σ* resonances can, in principle, result in ultrafast dissociation to C6H5 + I** and the subsequent autoionization of I**, but no evidence for this process is observed. The results are compared with our recent study of the resonant Auger decay of methyl iodide (CH3I).
    Language English
    Publishing date 2024-05-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/5.0203661
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Auger electron angular distributions following excitation or ionization from the Xe 3d and F 1s levels in xenon difluoride.

    Forbes, Ruaridh / Hockett, Paul / Powis, Ivan / Bozek, John D / Pratt, Stephen T / Holland, David M P

    Physical chemistry chemical physics : PCCP

    2022  Volume 24, Issue 3, Page(s) 1367–1379

    Abstract: Linearly polarized synchrotron radiation has been used to record polarization dependent, non-resonant Auger electron spectra of ... ...

    Abstract Linearly polarized synchrotron radiation has been used to record polarization dependent, non-resonant Auger electron spectra of XeF
    Language English
    Publishing date 2022-01-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 1476244-4
    ISSN 1463-9084 ; 1463-9076
    ISSN (online) 1463-9084
    ISSN 1463-9076
    DOI 10.1039/d1cp04797c
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Resonant Photoelectron Confinement in the SF

    Plésiat, Etienne / Canton, Sophie E / Bozek, John D / Decleva, Piero / Martín, Fernando

    The journal of physical chemistry. A

    2019  Volume 123, Issue 5, Page(s) 1062–1068

    Abstract: Recent thorough experimental activity aiming to generate high harmonics in the ... ...

    Abstract Recent thorough experimental activity aiming to generate high harmonics in the SF
    Language English
    Publishing date 2019-01-25
    Publishing country United States
    Document type Journal Article
    ISSN 1520-5215
    ISSN (online) 1520-5215
    DOI 10.1021/acs.jpca.8b12237
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A study of the valence photoelectron spectrum of uracil and mixed water-uracil clusters.

    Mattioli, Giuseppe / Avaldi, Lorenzo / Bolognesi, Paola / Casavola, Annarita / Morini, Filippo / Van Caekenberghe, Thomas / Bozek, John D / Castrovilli, Mattea C / Chiarinelli, Jacopo / Domaracka, Alicja / Indrajith, Suvasthika / Maclot, Sylvain / Milosavljević, Aleksandar R / Nicolafrancesco, Chiara / Nicolas, Christophe / Rousseau, Patrick

    The Journal of chemical physics

    2023  Volume 158, Issue 11, Page(s) 114301

    Abstract: The valence ionization of uracil and mixed water-uracil clusters has been studied experimentally and by ab initio calculations. In both measurements, the spectrum onset shows a red shift with respect to the uracil molecule, with the mixed cluster ... ...

    Abstract The valence ionization of uracil and mixed water-uracil clusters has been studied experimentally and by ab initio calculations. In both measurements, the spectrum onset shows a red shift with respect to the uracil molecule, with the mixed cluster characterized by peculiar features unexplained by the sum of independent contributions of the water or uracil aggregation. To interpret and assign all the contributions, we performed a series of multi-level calculations, starting from an exploration of several cluster structures using automated conformer-search algorithms based on a tight-binding approach. Ionization energies have been assessed on smaller clusters via a comparison between accurate wavefunction-based approaches and cost-effective DFT-based simulations, the latter of which were applied to clusters up to 12 uracil and 36 water molecules. The results confirm that (i) the bottom-up approach based on a multilevel method [Mattioli et al. Phys. Chem. Chem. Phys. 23, 1859 (2021)] to the structure of neutral clusters of unknown experimental composition converges to precise structure-property relationships and (ii) the coexistence of pure and mixed clusters in the water-uracil samples. A natural bond orbital (NBO) analysis performed on a subset of clusters highlighted the special role of H-bonds in the formation of the aggregates. The NBO analysis yields second-order perturbative energy between the H-bond donor and acceptor orbitals correlated with the calculated ionization energies. This sheds light on the role of the oxygen lone-pairs of the uracil CO group in the formation of strong H-bonds, with a stronger directionality in mixed clusters, giving a quantitative explanation for the formation of core-shell structures.
    Language English
    Publishing date 2023-02-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/5.0135574
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Dynamics of core-excited ammonia: disentangling fragmentation pathways by complementary spectroscopic methods.

    Travnikova, Oksana / Hosseini, Farzad / Marchenko, Tatiana / Guillemin, Renaud / Ismail, Iyas / Moussaoui, Roba / Journel, Loïc / Milosavljević, Aleksandar R / Bozek, John D / Kukk, Edwin / Püttner, Ralph / Piancastelli, Maria Novella / Simon, Marc

    Physical chemistry chemical physics : PCCP

    2022  

    Abstract: Fragmentation dynamics of core-excited isolated ammonia molecules is studied by two different and complementary experimental methods, high-resolution resonant Auger spectroscopy and electron energy-selected Auger electron-photoion coincidence ... ...

    Abstract Fragmentation dynamics of core-excited isolated ammonia molecules is studied by two different and complementary experimental methods, high-resolution resonant Auger spectroscopy and electron energy-selected Auger electron-photoion coincidence spectroscopy (AEPICO). The combined use of these two techniques allows obtaining information on different dissociation patterns, in particular fragmentation before relaxation, often called ultrafast dissociation (UFD), and fragmentation after relaxation. The resonant Auger spectra contain the spectral signature of both molecular and fragment final states, and therefore can provide information on all events occurring during the core-hole lifetime, in particular fragmentation before relaxation. Coincidence measurements allow correlating Auger electrons with ionic fragments from the same molecule, and relating the ionic fragments to specific Auger final electronic states, and yield additional information on which final states are dissociative, and which ionic fragments can be produced in timescales either corresponding to the core-hole lifetime or longer. Furthermore, we show that by the combined use of two complementary experimental techniques we are able to identify more electronic states of the NH
    Language English
    Publishing date 2022-11-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 1476244-4
    ISSN 1463-9084 ; 1463-9076
    ISSN (online) 1463-9084
    ISSN 1463-9076
    DOI 10.1039/d2cp03488c
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Electronic Structure and Solvation Effects from Core and Valence Photoelectron Spectroscopy of Serum Albumin.

    Renault, Jean-Philippe / Huart, Lucie / Milosavljević, Aleksandar R / Bozek, John D / Palaudoux, Jerôme / Guigner, Jean-Michel / Marichal, Laurent / Leroy, Jocelyne / Wien, Frank / Hervé Du Penhoat, Marie-Anne / Nicolas, Christophe

    International journal of molecular sciences

    2022  Volume 23, Issue 15

    Abstract: X-ray photoelectron spectroscopy of bovine serum albumin (BSA) in a liquid jet is used to investigate the electronic structure of a solvated protein, yielding insight into charge transfer mechanisms in biological systems in their natural environment. No ... ...

    Abstract X-ray photoelectron spectroscopy of bovine serum albumin (BSA) in a liquid jet is used to investigate the electronic structure of a solvated protein, yielding insight into charge transfer mechanisms in biological systems in their natural environment. No structural damage was observed in BSA following X-ray photoelectron spectroscopy in a liquid jet sample environment. Carbon and nitrogen atoms in different chemical environments were resolved in the X-ray photoelectron spectra of both solid and solvated BSA. The calculations of charge distributions demonstrate the difficulty of assigning chemical contributions in complex systems in an aqueous environment. The high-resolution X-ray core electron spectra recorded are unchanged upon solvation. A comparison of the valence bands of BSA in both phases is also presented. These bands display a higher sensitivity to solvation effects. The ionization energy of the solvated BSA is determined at 5.7 ± 0.3 eV. Experimental results are compared with theoretical calculations to distinguish the contributions of various molecular components to the electronic structure. This comparison points towards the role of water in hole delocalization in proteins.
    MeSH term(s) Electronics ; Photoelectron Spectroscopy ; Serum Albumin ; Serum Albumin, Bovine ; Water/chemistry
    Chemical Substances Serum Albumin ; Water (059QF0KO0R) ; Serum Albumin, Bovine (27432CM55Q)
    Language English
    Publishing date 2022-07-26
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms23158227
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  8. Article ; Online: Alternative Pathway to Double-Core-Hole States.

    Ismail, Iyas / Ferté, Anthony / Penent, Francis / Guillemin, Renaud / Peng, Dawei / Marchenko, Tatiana / Travnikova, Oksana / Inhester, Ludger / Taïeb, Richard / Verma, Abhishek / Velasquez, Nicolas / Kukk, Edwin / Trinter, Florian / Koulentianos, Dimitris / Mazza, Tommaso / Baumann, Thomas M / Rivas, Daniel E / Ovcharenko, Yevheniy / Boll, Rebecca /
    Dold, Simon / De Fanis, Alberto / Ilchen, Markus / Meyer, Michael / Goldsztejn, Gildas / Li, Kai / Doumy, Gilles / Young, Linda / Sansone, Giuseppe / Dörner, Reinhard / Piancastelli, Maria Novella / Carniato, Stéphane / Bozek, John D / Püttner, Ralph / Simon, Marc

    Physical review letters

    2024  Volume 131, Issue 25, Page(s) 253201

    Abstract: Excited double-core-hole states of isolated water molecules resulting from the sequential absorption of two x-ray photons have been investigated. These states are formed through an alternative pathway, where the initial step of core ionization is ... ...

    Abstract Excited double-core-hole states of isolated water molecules resulting from the sequential absorption of two x-ray photons have been investigated. These states are formed through an alternative pathway, where the initial step of core ionization is accompanied by the shake-up of a valence electron, leading to the same final states as in the core-ionization followed by core-excitation pathway. The capability of the x-ray free-electron laser to deliver very intense, very short, and tunable light pulses is fully exploited to identify the two different pathways.
    Language English
    Publishing date 2024-01-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.131.253201
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  9. Article ; Online: NEXAFS and MS-AES spectroscopy of the C 1s and Cl 2p excitation and ionization of chlorobenzene: Production of dicationic species.

    Coutinho, Lúcia H / de A Ribeiro, Fabio / Tenorio, Bruno N C / Coriani, Sonia / Dos Santos, Antonio C F / Nicolas, Christophe / Milosavljevic, Aleksandar R / Bozek, John D / Wolff, Wania

    Physical chemistry chemical physics : PCCP

    2021  Volume 23, Issue 48, Page(s) 27484–27497

    Abstract: We report on single- and double-charge photofragment formation by synchrotron radiation, following C 1s core excitation and ionization and Cl 2p inner excitation and ionization of chlorobenzene, ... ...

    Abstract We report on single- and double-charge photofragment formation by synchrotron radiation, following C 1s core excitation and ionization and Cl 2p inner excitation and ionization of chlorobenzene, C
    Language English
    Publishing date 2021-12-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 1476244-4
    ISSN 1463-9084 ; 1463-9076
    ISSN (online) 1463-9084
    ISSN 1463-9076
    DOI 10.1039/d1cp03121j
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  10. Article ; Online: Water-biomolecule clusters studied by photoemission spectroscopy and multilevel atomistic simulations: hydration or solvation?

    Mattioli, Giuseppe / Avaldi, Lorenzo / Bolognesi, Paola / Bozek, John D / Castrovilli, Mattea C / Chiarinelli, Jacopo / Domaracka, Alicja / Indrajith, Suvasthika / Maclot, Sylvain / Milosavljević, Aleksandar R / Nicolafrancesco, Chiara / Rousseau, Patrick

    Physical chemistry chemical physics : PCCP

    2021  Volume 23, Issue 28, Page(s) 15049–15058

    Abstract: The properties of mixed water-uracil nanoaggregates have been probed by core electron-photoemission measurements to investigate supramolecular assembly in the gas phase driven by weak interactions. The interpretation of the measurements has been assisted ...

    Abstract The properties of mixed water-uracil nanoaggregates have been probed by core electron-photoemission measurements to investigate supramolecular assembly in the gas phase driven by weak interactions. The interpretation of the measurements has been assisted by multilevel atomistic simulations, based on semi-empirical tight-binding and DFT-based methods. Our protocol established a positive-feedback loop between experimental and computational techniques, which has enabled a sound and detailed atomistic description of such complex heterogeneous molecular aggregates. Among biomolecules, uracil offers interesting and generalized skeletal features; its structure encompasses an alternation of hydrophilic H-bond donor and acceptor sites and hydrophobic moieties, typical in biomolecular systems, that induces a supramolecular core-shell-like organization of the mixed clusters with a water core and an uracil shell. This structure is far from typical models of both solid-state hydration, with water molecules in defined positions, or liquid solvation, where disconnected uracil molecules are completely surrounded by water.
    MeSH term(s) Density Functional Theory ; Hydrogen Bonding ; Hydrophobic and Hydrophilic Interactions ; Models, Molecular ; Nanostructures/chemistry ; Photoelectron Spectroscopy ; Solvents/chemistry ; Spectrometry, Fluorescence ; Thermodynamics ; Uracil/chemistry ; Water/chemistry
    Chemical Substances Solvents ; Water (059QF0KO0R) ; Uracil (56HH86ZVCT)
    Language English
    Publishing date 2021-07-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 1476244-4
    ISSN 1463-9084 ; 1463-9076
    ISSN (online) 1463-9084
    ISSN 1463-9076
    DOI 10.1039/d1cp02031e
    Database MEDical Literature Analysis and Retrieval System OnLINE

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