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First glimpse of the soft x-ray induced excited spin-state trapping effect dynamics on spin cross-over molecules.
Davesne, V; Gruber, M; Miyamachi, T; Da Costa, V; Boukari, S; Scheurer, F; Joly, L; Ohresser, P; Otero, E; Choueikani, F; Gaspar, A B; Real, J A; Wulfhekel, W; Bowen, M; Beaurepaire, E.
Afiliación
  • Davesne V; Institut de Physique et de Chimie des Matériaux de Strasbourg, Université de Strasbourg, CNRS UMR 7504 23 rue du Loess, 67034 Strasbourg, France. vincent.davesne@ipcms.unistra.fr
J Chem Phys ; 139(7): 074708, 2013 Aug 21.
Article en En | MEDLINE | ID: mdl-23968108
The dynamics of the soft x-ray induced excited spin state trapping (SOXIESST) effect of Fe(phen)2(NCS)2 (Fe-phen) powder have been investigated by x-ray absorption spectroscopy (XAS) using the total electron yield method, in a wide temperature range. The low-spin (LS) state is excited into the metastable high-spin (HS) state at a rate that depends on the intensity of the x-ray illumination it receives, and both the temperature and the intensity of the x-ray illumination will affect the maximum HS proportion that is reached. We find that the SOXIESST HS spin state transforms back to the LS state at a rate that is similar to that found for the light induced excited spin state trapping (LIESST) effect. We show that it is possible to use the SOXIESST effect in combination with the LIESST effect to investigate the influence of cooperative behavior on the dynamics of both effects. To investigate the impact of molecular cooperativity, we compare our results on Fe-phen with those obtained for Fe{[Me2Pyrz]3BH}2 (Fe-pyrz) powder, which exhibits a similar thermal transition temperature but with a hysteresis. We find that, while the time constant of the dynamic is identical for both molecules, the SOXIESST effect is less efficient at exciting the HS state in Fe-pyrz than in Fe-phen.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2013 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2013 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos