Spontaneous Charge Separation and Recombination ...
Type de document :
Article dans une revue scientifique
DOI :
URL permanente :
Titre :
Spontaneous Charge Separation and Recombination Induced by Tetracene Incorporation in Pores of Acidic HnZSM-5 Zeolites
Auteur(s) :
Marquis, Séverine [Auteur]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Moissette, Alain [Auteur]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Hureau, Matthieu [Auteur]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Vezin, Herve [Auteur]
Laboratoire de Chimie Organique et Macromoleculaire [UMR CNRS 8009]
Brémard, Claude [Auteur]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Moissette, Alain [Auteur]

Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Hureau, Matthieu [Auteur]

Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Vezin, Herve [Auteur]

Laboratoire de Chimie Organique et Macromoleculaire [UMR CNRS 8009]
Brémard, Claude [Auteur]
Centre d'Etudes et de Recherches Lasers et Applications [CERLA]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Titre de la revue :
The Journal of Physical Chemistry C
Nom court de la revue :
J. Phys. Chem. C
Numéro :
111
Pagination :
17346-17356
Éditeur :
American Chemical Society (ACS)
Date de publication :
2007-10-30
ISSN :
1932-7455
Mot(s)-clé(s) en anglais :
Sorption
Zeolites
Molecules
Ionization
Cations
Zeolites
Molecules
Ionization
Cations
Discipline(s) HAL :
Chimie/Chimie théorique et/ou physique
Résumé en anglais : [en]
In situ CW-EPR and diffuse reflectance UV−visible spectroscopy were used to monitor the spontaneous incorporation of ACENE-4 or tetracene (C18H12) in the medium-pore MnZSM-5 zeolites [Mn(AlO2)n(SiO2)96-n; MNa+, H+; n = ...
Lire la suite >In situ CW-EPR and diffuse reflectance UV−visible spectroscopy were used to monitor the spontaneous incorporation of ACENE-4 or tetracene (C18H12) in the medium-pore MnZSM-5 zeolites [Mn(AlO2)n(SiO2)96-n; MNa+, H+; n = 3.4, 6.6] by direct exposure under dry and inert atmosphere of solid ACENE-4 to dehydrated porous materials without any solvent. The sorption of the large ACENE-4 molecule with relatively low ionization potential (6.97 eV) occurs in Brønsted acidic HnZSM-5 zeolites according to a complex and slow reaction sequence including protonation, charge separation, hole transfer, and charge recombination while ACENE-4 is incorporated as an intact molecule in nonacidic NanZSM-5. After a long organization period, ACENE-4 lies in the straight channel in front of sodium cation in close proximity of Al framework atom as simulated by Monte Carlo calculations. The multivariate curve resolution (MCR) analysis of the huge DRUVv spectra set recorded during the ACENE-4 sorption course in acidic HnZSM-5 resolved successfully the specific absorption spectra and respective concentrations of all species as function of time. HACENE-4+@Hn-1ZSM-5- protonated species and ACENE-4•+@HnZSM-5•- radical pair are generated in the first steps of sorption while a long-lived ACENE-4@HnZSM-5•-•+ electron−hole pair is formed through hole transfer and recombines slowly to ACENE-4@HnZSM-5 without any protonation. Two-dimensional hyperfine-sublevel correlation (2D-HYSCORE) experiments reveal the structural surroundings of the unpaired electrons through the proper assignment of unpaired electron couplings with 1H, 29Si, and 27Al nuclei. The tight fit between the rod shape ACENE-4 and the pore size of ZSM-5 zeolites combined with the efficient polarizing effect of proton and aluminum electron trapping sites are the most important factors responsible for the stabilization of the electron−hole moiety and hinder the charge recombination efficiently.Lire moins >
Lire la suite >In situ CW-EPR and diffuse reflectance UV−visible spectroscopy were used to monitor the spontaneous incorporation of ACENE-4 or tetracene (C18H12) in the medium-pore MnZSM-5 zeolites [Mn(AlO2)n(SiO2)96-n; MNa+, H+; n = 3.4, 6.6] by direct exposure under dry and inert atmosphere of solid ACENE-4 to dehydrated porous materials without any solvent. The sorption of the large ACENE-4 molecule with relatively low ionization potential (6.97 eV) occurs in Brønsted acidic HnZSM-5 zeolites according to a complex and slow reaction sequence including protonation, charge separation, hole transfer, and charge recombination while ACENE-4 is incorporated as an intact molecule in nonacidic NanZSM-5. After a long organization period, ACENE-4 lies in the straight channel in front of sodium cation in close proximity of Al framework atom as simulated by Monte Carlo calculations. The multivariate curve resolution (MCR) analysis of the huge DRUVv spectra set recorded during the ACENE-4 sorption course in acidic HnZSM-5 resolved successfully the specific absorption spectra and respective concentrations of all species as function of time. HACENE-4+@Hn-1ZSM-5- protonated species and ACENE-4•+@HnZSM-5•- radical pair are generated in the first steps of sorption while a long-lived ACENE-4@HnZSM-5•-•+ electron−hole pair is formed through hole transfer and recombines slowly to ACENE-4@HnZSM-5 without any protonation. Two-dimensional hyperfine-sublevel correlation (2D-HYSCORE) experiments reveal the structural surroundings of the unpaired electrons through the proper assignment of unpaired electron couplings with 1H, 29Si, and 27Al nuclei. The tight fit between the rod shape ACENE-4 and the pore size of ZSM-5 zeolites combined with the efficient polarizing effect of proton and aluminum electron trapping sites are the most important factors responsible for the stabilization of the electron−hole moiety and hinder the charge recombination efficiently.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
CNRS
Collections :
Date de dépôt :
2021-06-18T09:09:43Z
2021-10-12T10:38:39Z
2021-10-12T10:38:39Z