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Autor(en) / Beteiligte
Titel
Near-infrared absorption and radiative cooling of naphthalene dimers (CH)
Ist Teil von
  • Physical chemistry chemical physics : PCCP, 2024-07, Vol.26 (27), p.18571-18583
Erscheinungsjahr
2024
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • The radiative cooling of naphthalene dimer cations, (C 10 H 8 ) 2 + was studied experimentally through action spectroscopy using two different electrostatic ion-beam storage rings, DESIREE in Stockholm and Mini-Ring in Lyon. The spectral characteristics of the charge resonance (CR) band were observed to vary significantly with a storage time of up to 30 seconds in DESIREE. In particular, the position of the CR band shifts to the blue, with specific times (inverse of rates) of 0.64 s and 8.0 s in the 0-5 s and 5-30 s storage time ranges, respectively. These long-time scales indicate that the internal energy distribution of the stored ions evolves by vibrational radiative cooling, which is consistent with the absence of fast radiative cooling via recurrent fluorescence for (C 10 H 8 ) 2 + . Density functional based tight binding calculations with local excitations and configuration interactions (DFTB-EXCI) were used to simulate the absorption spectrum for ion temperatures between 10 and 500 K. The evolution of the bandwidth and position with temperature is in qualitative agreement with the experimental findings. Furthermore, these calculations yielded linear temperature dependencies for both the shift and the broadening. Combining the relationship between the CR band position and the ion temperature with the results of the statistical model, we demonstrate that the observed blue shift can be used to determine the radiative cooling rate of (C 10 H 8 ) 2 + . Time-dependent blue shift of action spectra in storage rings are used to determine the radiative cooling rate of naphthalene dimer cations, (C 10 H 8 ) 2 + . DFTB-EXCI and Monte-Carlo models are successful in reproducing infrared cooling temporal evolution.
Sprache
Identifikatoren
ISSN: 1463-9076
eISSN: 1463-9084
DOI: 10.1039/d4cp01200c
Titel-ID: cdi_rsc_primary_d4cp01200c
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