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Sökning: WFRF:(Cederquist H.)

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1.
  • Najeeb, P. K., et al. (författare)
  • Spontaneous decay of small carbon cluster dianions C-n(2-) (n=7-11)
  • 2020
  • Ingår i: Journal of Physics, Conference Series, Vol 1412, Article 232014. - : IOP Publishing. - 1742-6588 .- 1742-6596.
  • Konferensbidrag (refereegranskat)abstract
    • We have studied the stabilities of small carbon dianion clusters, C-n(2-) (n=7-11) in the cryogenic electrostatic ion storage ring, DESIREE. We observe spontaneous electron emission for tens of milliseconds, where dianions containing an even number of carbons decay slower in comparison to their neighbouring cluster sizes. For all the systems considered here, we find that there is a component which is stable at least on the time scales of hundreds of milliseconds.
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4.
  • Hartman, Henrik, et al. (författare)
  • Negative ion relaxation and reactions in a cryogenic storage ring
  • 2020
  • Ingår i: Journal of Physics: Conference Series Vol 1412. - : IOP Publishing. - 1742-6588 .- 1742-6596.
  • Konferensbidrag (refereegranskat)abstract
    • An overview of recent experimental results of studies of negative atomic and molecular ions in the Double ElectroStatic Ion-Ring ExpEriment, DESIREE is given. Metastable level lifetimes in atomic negative ions have been measured by time-dependent laser photodetachment. Rotational relaxation of diatomic anions is studied by near-threshold photodetachment. Spontaneous decays of small metal cluster anions by electron emission and fragmentation is studied with decay-channel specificity. Finally, mutual neutralisation of pairs of negative and positive ions has been investigated with initial and final state selectivity.
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5.
  • Schmidt, HT, et al. (författare)
  • Recoil-ion momentum distributions for transfer ionization in fast proton-He collisions
  • 2005
  • Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics. - : American physical society. - 1050-2947 .- 1094-1622. ; 72:1
  • Tidskriftsartikel (refereegranskat)abstract
    • We present high-luminosity experimental investigations of the transfer ionization (TI:p+He -> H-0+He2++e(-)) process in collisions between fast protons and neutral helium atoms in the earlier inaccessibly high-energy range 1.4-5.8 MeV. The protons were stored in the heavy-ion storage and cooler ring CRYRING, where they intersected a narrow supersonic helium gas jet. We discuss the longitudinal recoil-ion momentum distribution, as measured by means of cold-target recoil-ion momentum spectroscopy and find that this distribution splits into two completely separated peaks at the high end of our energy range. These separate contributions are discussed in terms of the earlier proposed Thomas TI (TTI) and kinematic TI mechansims. The cross section of the TTI process is found to follow a sigma proportional to v(-b) dependence with b=10.78 +/- 0.27 in accordance with the expected v(-11) asymptotic behavior. Further, we discuss the probability for shake-off accompanying electron transfer and the relation of this TI mechanism to photodouble ionization. Finally the influence of the initial-state electron velocity distribution on the TTI process is discussed.
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6.
  • Stockett, M.H., et al. (författare)
  • Spontaneous decay of small copper cluster anions, Cu_N^-, N = 3 - 6
  • 2015
  • Ingår i: Journal of Physics, Conference Series. - 1742-6588 .- 1742-6596. ; 635
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • We have measured the spontaneous neutral particle emission from beams of copper cluster anions (Cu_N, N = 3 to 6) stored in an electrostatic storage ring. These experiments have show that multiple structural isomers may be present in the beam.
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10.
  • Chartkunchand, K. C., et al. (författare)
  • Lifetimes of bound excited states of Pt-
  • 2017
  • Ingår i: Journal of Physics: Conference Series, Vol. 875, no. 022051. - : IOP Publishing. - 1742-6588.
  • Konferensbidrag (refereegranskat)abstract
    • Measurements of the radiative lifetimes of the two excited states of the platinum anion Pt- are presented. Pt- ions stored in the cryogenic ion storage ring DESIREE were photodetached at different photon wavelengths and the resulting yield of neutral Pt measured as a function of time was recorded. Analysis of the neutral decay curves show a 2.54 +/- 0.10 s lifetime for the higher-lying 5d(10)6(s) S-2(1/2) excited state and a lifetime in the range of 50-200 ms for the lower- lying 5d(9)6(s)(2) D-2(3/2) excited state. This is the first study to report the lifetime of a bound anion excited state with an electron configuration different from that of the anion ground state.
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11.
  • Eklund, G., et al. (författare)
  • Final state resolved mutual neutralization of Li+ and D-
  • 2020
  • Ingår i: 31St International Conference On Photonic, Electronic And Atomic Collisions (Icpeac Xxxi). - : IOP PUBLISHING LTD.
  • Konferensbidrag (refereegranskat)abstract
    • We have performed a merged beam experiment on mutual neutralization of Li+ and D-, at center of mass energies close to 0 eV using the DESIREE storage rings. The final state channels Li(3s) and Li(3p+3d) are resolved and the branching ratio is found to be more equal than predicted from theoretical models.
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17.
  • Kristiansson, M. K., et al. (författare)
  • Photodetachment Studies of Ir- Ions at DESIREE
  • 2020
  • Ingår i: Journal of Physics: Conference Series, Volume 1412, Structure / Spectroscopy. - : IOP. - 1742-6588.
  • Konferensbidrag (refereegranskat)abstract
    • Anions of iridium were stored in the cryogenic storage ring, DESIREE [1, 2, 3] and investigated using laser photodetachment. The ions were stored for up to 2000 seconds and the relaxation of several metastable states were studied by selecting different photon energies. The threshold of the previously not observed P-3(2) level is located and the lifetime of this sate is found to be longer than the storage time of the ion beam. We also find that a state exists higher in energy than the previously known level with a lifetime in the range of hundreds of milliseconds.
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25.
  • Tomita, S., et al. (författare)
  • Lifetimes of C602- and C702- dianions in a storage ring
  • 2006
  • Ingår i: J. Chem. Phys.. - : AIP Publishing. - 0021-9606. ; 124
  • Tidskriftsartikel (refereegranskat)abstract
    • C602- and C702- dianions have been produced by electrospray of the monoanions and subsequent electron pickup in a Na vapor cell. The dianions were stored in an electrostatic ring and their decay by electron emission was measured up to 1 s after injection. While C ions are stable on this time scale, except for a small fraction of the ions which have been excited by gas collisions, most of the C ions decay on a millisecond time scale, with a lifetime depending strongly on their internal temperature. The results can be modeled as decay by electron tunneling through a Coulomb barrier, mainly from thermally populated triplet states about 120 meV above a singlet ground state. At times longer than about 100 ms, the absorption of blackbody radiation plays an important role for the decay of initially cold ions. The tunneling rates obtained from the modeling, combined with WKB estimates of the barrier penetration, give a ground-state energy 200±30 meV above the energy of the monoanion plus a free electron and a ground-state lifetime of the order of 20 s.
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27.
  • Wethekam, S., et al. (författare)
  • Resonant electron capture by C-60 ions at a metal surface with projected band gap
  • 2010
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 81:12, s. 121416-
  • Tidskriftsartikel (refereegranskat)abstract
    • C-60(+) and C-60(2+) ions are scattered under grazing incidence from an atomically clean and flat Be(0001) surface at kilo-electron-volt energies. Distances for electron transfer are deduced from shifts of angular distributions for incident C-60(+) and C-60(2+) projectiles, which reflect changes in the interaction potentials at the instants of electron transfers. These distances are consistent with classical over-the-barrier model results indicating that the suppression of charge transfer, observed for atomic projectiles in front of metal surfaces with a projected band gap, is absent for fullerenes.
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28.
  • Wolf, Michael, et al. (författare)
  • PHOTO-STABILITY OF SUPER-HYDROGENATED PAHs DETERMINED BY ACTION SPECTROSCOPY EXPERIMENTS
  • 2016
  • Ingår i: Astrophysical Journal. - 0004-637X .- 1538-4357. ; 832:1
  • Tidskriftsartikel (refereegranskat)abstract
    • We have investigated the photo-stability of pristine and super-hydrogenated pyrene cations (C16H10+m+, m = 0, 6, or 16) by means of gas-phase action spectroscopy. Optical absorption spectra and photoinduced dissociation mass spectra are presented. By measuring the yield of mass-selected photo-fragment ions as a function of laser pulse intensity, the number of photons (and hence the energy) needed for fragmentation of the carbon backbone was determined. Backbone fragmentation of pristine pyrene ions (C16H10+) requires absorption of three photons of energy just below 3 eV, whereas super-hydrogenated hexahydropyrene (C16H16+) must absorb two such photons and fully hydrogenated hexadecahydropyrene (C16H26+) only a single photon. These results are consistent with previously reported dissociation energies for these ions. Our experiments clearly demonstrate that the increased heat capacity from the additional hydrogen atoms does not compensate for the weakening of the carbon backbone when pyrene is hydrogenated. In photodissociation regions, super-hydrogenated Polycyclic Aromatic Hydrocarbons (PAHs) have been proposed to serve as catalysts for H-2 formation. Our results indicate that carbon backbone fragmentation may be a serious competitor to H-2 formation at least for small hydrogenated PAHs like pyrene.
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31.
  • Zettergren, H., et al. (författare)
  • Even-odd effects in the ionization cross sections of [C60]2 and [C60C70] dimers
  • 2007
  • Ingår i: Physical Review A. Atomic, Molecular, and Optical Physics. - 1050-2947 .- 1094-1622. ; 75:5, s. 051201-
  • Tidskriftsartikel (refereegranskat)abstract
    • We report strong even-odd effects in multiple ionization yields of van der Waals dimers in slowXe30+ + ͓C60͔2͓͑C60C70͔͒ →  ̄ + ͓C60͔2r+͓͑C60C70͔r+͒ electron-transfer collisions as functions of r Յ 7. Thisbehavior may be due to even-odd variations in the sequences of dimer ionization energies as calculated with anelectrostatic model including an electrical fullerene-fullerene contact at the 19a0 center-center separation in͓C60͔2+. Prompt dissociations predominantly yield intact fullerenes ͓C60͔2r+ → C60r1+ + C60r2+ in the same͑r1 = r2, even r͒ or nearby ͑r1 = r2 ± 1, odd r Ͼ 1͒ charge states.
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34.
  • Zettergren, H., et al. (författare)
  • Stabilities of multiply charged dimers and clusters of fullerenes
  • 2007
  • Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 126:22, s. 224303-
  • Tidskriftsartikel (refereegranskat)abstract
    • The authors find even-odd variations as functions of r (...+[C60]2(r+)([C60C70](r+)) electron-transfer collisions. This even-odd behavior is in sharp contrast to the smooth one for fullerene monomers and may be related to even-odd effects in dimer ionization energies in agreement with results from an electrostatic model. The kinetic energy releases for dimer dissociations [predominantly yielding intact fullerenes [C60]2(r+)-->C60(r1+)+C60(r2+) in the same (r1=r2) or nearby (r1=r2+/-1) charge states] are found to be low in comparison with the corresponding model results indicating that internal excitations of the separating (intact) fullerenes are important. Experimental appearance sizes for the heavier clusters of fullerenes [C60]n(r+) (n>3 and r=2-5) compare well with predictions from a new nearest-neighbor model assuming that r unit charges in [C60]n(r+) are localized to r C60 molecules such that the Coulomb energy of the system is minimized. The system is then taken to be stable if (i) two (singly) charged C60 are not nearest neighbors and (ii) the r C60(+) molecules have binding energies to their neutral nearest neighbors which are larger than the repulsive energies for the (r-1) C60(+)-C60(+) pairs. Essential ingredients in the nearest-neighbor model are cluster geometries and the present results on dimer stabilities.
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35.
  • Andersson, Ulrika, et al. (författare)
  • Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer
  • 2014
  • Ingår i: Neuro-Oncology. - : Oxford University Press. - 1522-8517 .- 1523-5866. ; 16:10, s. 1333-1340
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Although familial susceptibility to glioma is known, the genetic basis for this susceptibility remains unidentified in the majority of glioma-specific families. An alternative approach to identifying such genes is to examine cancer pedigrees, which include glioma as one of several cancer phenotypes, to determine whether common chromosomal modifications might account for the familial aggregation of glioma and other cancers. Methods: Germline rearrangements in 146 glioma families (from the Gliogene Consortium; http://www.gliogene.org/) were examined using multiplex ligation-dependent probe amplification. These families all had at least 2 verified glioma cases and a third reported or verified glioma case in the same family or 2 glioma cases in the family with at least one family member affected with melanoma, colon, or breast cancer. The genomic areas covering TP53, CDKN2A, MLH1, and MSH2 were selected because these genes have been previously reported to be associated with cancer pedigrees known to include glioma. Results: We detected a single structural rearrangement, a deletion of exons 1-6 in MSH2, in the proband of one family with 3 cases with glioma and one relative with colon cancer. Conclusions: Large deletions and duplications are rare events in familial glioma cases, even in families with a strong family history of cancers that may be involved in known cancer syndromes.
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36.
  • Bernard, J, et al. (författare)
  • A
  • 2008
  • Ingår i: Rev Sci Instrum. - 0034-6748. ; 79:7, s. 075109-
  • Tidskriftsartikel (refereegranskat)
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37.
  • Chartkunchand, C, et al. (författare)
  • Measuring the 2D3/2 Ni− excited state lifetime in DESIREE
  • 2015
  • Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 635
  • Konferensbidrag (refereegranskat)abstract
    • Experimental studies of the radiative lifetime of the sole excited state in the nickel anion are presented. Beams of Ni− stored in DESIREE at cryogenic temperatures were subject to photodetachment at different photon energies and the resulting neutrals collected. Preliminary analysis of the decay in neutral production yields a radiative lifetime of approximately 15 seconds for the 3d94s2 2D3/2 excited state.
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38.
  • Gatchell, Michael, et al. (författare)
  • Commissioning of the DESIREE storage rings - a new facility for cold ion-ion collisions
  • 2014
  • Ingår i: XXVIII International Conference on Photonic, Electronic and Atomic Collisions (ICPEAC 2013). - : Institute of Physics (IOP). ; 488:1
  • Konferensbidrag (refereegranskat)abstract
    • We report on the ongoing commissioning of the Double ElectroStatic Ion Ring ExpEriment, DESIREE, at Stockholm University. Beams of atomic carbon anions (C-) and smaller carbon anion molecules (C-2(-), C-3(-), C-4(-) etc.) have been produced in a sputter ion source, accelerated to 10 keV or 20 keV, and stored successfully in the two electrostatic rings. The rings are enclosed in a common vacuum chamber cooled to below 13 Kelvin. The DESIREE facility allows for studies of internally relaxed single isolated atomic, molecular and cluster ions and for collision experiments between cat-and anions down to very low center-of-mass collision energies (meV scale). The total thermal load of the vacuum chamber at this temperature is measured to be 32 W. The decay rates of stored ion beams have two components: a non-exponential component caused by the space charge of the beam itself which dominates at early times and an exponential term from the neutralization of the beam in collisions with residual gas at later times. The residual gas limited storage lifetime of carbon anions in the symmetric ring is over seven minutes while the 1/e lifetime in the asymmetric ring is measured to be about 30 seconds. Although we aim to improve the storage in the second ring, the number of stored ions are now sufficient for many merged beams experiments with positive and negative ions requiring milliseconds to seconds ion storage.
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39.
  • Gudmundsson, Magnus, et al. (författare)
  • Angular scattering in fast ion-atom electron transfer collisions : projectile wave diffraction and Thomas mechanisms
  • 2010
  • Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 43:18, s. 185209-
  • Tidskriftsartikel (refereegranskat)abstract
    • We report experimental angular differential cross sections for double-electron capture in He2+ + He collisions and single-electron capture in H+ + He collisions for the 1.3-12.5 MeV kinetic energy range. In all cases, the total cross sections are dominated by forward scattering peaks in d sigma/d Omega. The shapes and widths (but not the magnitudes) of these peaks are very similar for all energies and for capture of one or two electrons corresponding also to our measured linear increases in the transverse momentum transfers with increasing projectile velocities. These observations may be ascribed to diffraction limitations which are connected to electron transfer probabilities P(b) which are significant in limited regions of b only. For the H+ + He single-electron capture we observe two additional maxima in the angular differential cross sections. We conclude that while the secondary maxima at similar to 0.5 mrad probably have large contributions from the Thomas proton-electron-nucleus scattering mechanism, the third maxima at similar to 0.75 mrad are most likely mainly due to projectile de Broglie wave diffraction.
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40.
  • Kaminska, M, et al. (författare)
  • Storing keV negative ions for hours: Lifetime measurements in new time domains
  • 2015
  • Ingår i: Journal of Physics: Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 635
  • Konferensbidrag (refereegranskat)abstract
    • We have used one of the cryogenic ion storage rings of DESIREE to measure the lifetime of the 2P o 1/2 level in the sulfur anion to be 503 ± 43 seconds. This is orders of magnitude longer than any previously measured lifetime in a negatively charged ion.
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43.
  • Najeeb, P. K., 1986-, et al. (författare)
  • Stability and Cooling of the C72- Dianion
  • 2023
  • Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 131:11
  • Tidskriftsartikel (refereegranskat)abstract
    • We have studied the stability of the smallest long-lived all carbon molecular dianion (C72-) in new time domains and with a single ion at a time using a cryogenic electrostatic ion-beam storage ring. We observe spontaneous electron emission from internally excited dianions on millisecond timescales and monitor the survival of single colder C72- molecules on much longer timescales. We find that their intrinsic lifetime exceeds several minutes - 6 orders of magnitude longer than established from earlier experiments on C72-. This is consistent with our calculations of vertical electron detachment energies predicting one inherently stable isomer and one isomer which is stable or effectively stable behind a large Coulomb barrier for C72-→C7-+e- separation.
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44.
  • Najeeb, P. K., 1986-, et al. (författare)
  • Stability and Cooling of the C2−7 Dianion
  • 2023
  • Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 131:11
  • Tidskriftsartikel (refereegranskat)abstract
    • We have studied the stability of the smallest long-lived all carbon molecular dianion () in new time domains and with a single ion at a time using a cryogenic electrostatic ion-beam storage ring. We observe spontaneous electron emission from internally excited dianions on millisecond timescales and monitor the survival of single colder molecules on much longer timescales. We find that their intrinsic lifetime exceeds several minutes—6 orders of magnitude longer than established from earlier experiments on . This is consistent with our calculations of vertical electron detachment energies predicting one inherently stable isomer and one isomer which is stable or effectively stable behind a large Coulomb barrier for →+e− separation.
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45.
  • Thomas, Richard D., et al. (författare)
  • DESIREE : Physics with cold stored ion beams
  • 2015
  • Ingår i: DR2013. - : EDP Sciences. ; 84, s. 01004-01004
  • Konferensbidrag (refereegranskat)abstract
    • Here we will briefly describe the commissioning of the Double ElectroStatic Ion Ring ExpEriment (DESIREE) facility at Stockholm University, Sweden. This device uses purely electrostatic focussing and deflection elements and allows ion beams of opposite charge to be confined under extreme high vacuum and cryogenic conditions in separate rings and then merged over a common straight section. This apparatus allows for studies of interactions between cations and anions at very low and well-defined centre-of-mass energies (down to a few meV) and at very low internal temperatures (down to a few K).
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46.
  • Zettergren, Henning, et al. (författare)
  • Roadmap on dynamics of molecules and clusters in the gas phase
  • 2021
  • Ingår i: European Physical Journal D. - : Springer Science and Business Media LLC. - 1434-6060 .- 1434-6079. ; 75:5
  • Tidskriftsartikel (refereegranskat)abstract
    • This roadmap article highlights recent advances, challenges and future prospects in studies of the dynamics of molecules and clusters in the gas phase. It comprises nineteen contributions by scientists with leading expertise in complementary experimental and theoretical techniques to probe the dynamics on timescales spanning twenty order of magnitudes, from attoseconds to minutes and beyond, and for systems ranging in complexity from the smallest (diatomic) molecules to clusters and nanoparticles. Combining some of these techniques opens up new avenues to unravel hitherto unexplored reaction pathways and mechanisms, and to establish their significance in, e.g. radiotherapy and radiation damage on the nanoscale, astrophysics, astrochemistry and atmospheric science.
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47.
  • Allu, P. K. R., et al. (författare)
  • FoxK1 associated gene regulatory network in hepatic insulin action and its relationship to FoxO1 and insulin receptor mediated transcriptional regulation
  • 2023
  • Ingår i: Molecular Metabolism. - 2212-8778. ; 78
  • Tidskriftsartikel (refereegranskat)abstract
    • Objective: Insulin acts on the liver via changes in gene expression to maintain glucose and lipid homeostasis. This study aimed to the Forkhead box protein K1 (FOXK1) associated gene regulatory network as a transcriptional regulator of hepatic insulin action and to determine its role versus FoxO1 and possible actions of the insulin receptor at the DNA level.Methods: Genome-wide analysis of FoxK1 binding were studied by chromatin immunoprecipitation sequencing and compared to those for IR and FoxO1. These were validated by knockdown experiments and gene expression analysis.Results: Chromatin immunoprecipitation (ChIP) sequencing shows that FoxK1 binds to the proximal promoters and enhancers of over 4000 genes, and insulin enhances this interaction for about 75% of them. These include genes involved in cell cycle, senescence, steroid biosynthesis, autophagy, and metabolic regulation, including glucose metabolism and mitochondrial function and are enriched in a TGTTTAC consensus motif. Some of these genes are also bound by FoxO1. Comparing this FoxK1 ChIP-seq data to that of the insulin receptor (IR) reveals that FoxK1 may act as the transcription factor partner for some of the previously reported roles of IR in gene regulation, including for LARS1 and TIMM22, which are involved in rRNA processing and cell cycle.Conclusion: These data demonstrate that FoxK1 is an important regulator of gene expression in response to insulin in liver and may act in concert with FoxO1 and IR in regulation of genes in metabolism and other important biological pathways.(c) 2023 The Authors. Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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48.
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49.
  • Anderson, Emma K., 1986-, et al. (författare)
  • Fragmentation of and electron detachment from hot copper and silver dimer anions : A comparison
  • 2023
  • Ingår i: Physical Review A: covering atomic, molecular, and optical physics and quantum information. - 2469-9926 .- 2469-9934. ; 107:6
  • Tidskriftsartikel (refereegranskat)abstract
    • We measured the spontaneous decays of internally hot copper and silver dimer anions, and , stored in one of the two ion-beam storage rings of the Double Electrostatic Ion Ring Experiment (DESIREE) at Stockholm University. A coincidence detection technique was utilized enabling essentially background-free measurements of -> Cu + Cu- and -> Ag + Ag- fragmentation rates. Furthermore, the total rates of neutral decay products (monomers and dimers) were measured and the relative contributions of fragmentation and electron emission ( -> Cu2 + e- and -> Ag2 + e-) were deduced as functions of storage time. Fragmentation is completely dominant at early times. However, after about 20 ms of storage, electron emission is observed and becomes the leading decay path after 100 ms for both dimer anions. The branching ratios between fragmentation and electron emission (vibrationally assisted autodetachment processes) are very nearly the same for and Ag-2 throughout the present storage cycle of 10 seconds. This is surprising considering the difference between the electron affinities of the neutral dimers, Cu2 and Ag2, and the difference between the and the dissociation energies.
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50.
  • Bernard, Jérôme, et al. (författare)
  • Efficient radiative cooling of tetracene cations C18H12+ : absolute recurrent fluorescence rates as a function of internal energy
  • 2023
  • Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 25:15, s. 10726-10740
  • Tidskriftsartikel (refereegranskat)abstract
    • We have measured recurrent fluorescence (RF) cooling rates of internally hot tetracene cations, C18H12+, as functions of their storage times and internal energies in two different electrostatic ion-beam storage rings – the cryogenic ring DESIREE with a circumference of 8.6 meters in Stockholm and the much smaller room temperature ring Mini-Ring in Lyon, which has a circumference of 0.71 meters. The RF rates were measured to be as high as 150 to 1000 s−1 for internal energies in the 7 to 9.4 eV energy range, where we have probed the time evolution of the internal energy distribution with nanosecond laser pulses with a 1 kHz repetition rate. These RF rates are found to be significantly higher than those of previously investigated smaller PAHs such as e.g. anthracene and naphthalene, for which the lowest non-forbidden electronic excited state, the D2 state, is populated with a smaller probability by inverse internal conversion. Furthermore, the D2–D0 transition rate is smaller for these smaller molecules than for tetracene. The complementary features of the two storage rings allow for RF rate measurements in a broader internal energy range than has been possible before. The smaller sampling period of about 6 μs in Mini-Ring is ideal to study the cooling dynamics of the hotter ions that decay fast, whereas DESIREE with a sampling period of about 60 μs is better suited to study the colder ions that decay on longer timescales ranging up to hundreds of milliseconds. The excellent agreement between the two series of measurements in the region where they overlap demonstrates the complementarity of the two electrostatic ion-beam storage rings.
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