Synergy in photomagnetic/ferromagnetic sub-50 nm core-multishell nanoparticles
DIA, Nada
Ecole Doctorale des Sciences et de Technologie
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Ecole Doctorale des Sciences et de Technologie
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
LISNARD, Laurent
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Institut Parisien de Chimie Moléculaire [IPCM]
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Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Institut Parisien de Chimie Moléculaire [IPCM]
DIA, Nada
Ecole Doctorale des Sciences et de Technologie
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Ecole Doctorale des Sciences et de Technologie
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
LISNARD, Laurent
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Institut Parisien de Chimie Moléculaire [IPCM]
< Réduire
Institut de Chimie Moléculaire et des Matériaux d'Orsay [ICMMO]
Institut Parisien de Chimie Moléculaire [IPCM]
Langue
en
Article de revue
Ce document a été publié dans
Inorganic Chemistry. 2013-09-16, vol. 52, n° 18, p. 10264-10274
American Chemical Society
Résumé en anglais
Based on nickel hexacyanidochromate and cobalt hexacyanidoferrate Prussian blue analogues, two series of photomagnetic/ferromagnetic sub-50 nm core multishell coordination nanoparticles have been synthesized in a surfactant-free ...Lire la suite >
Based on nickel hexacyanidochromate and cobalt hexacyanidoferrate Prussian blue analogues, two series of photomagnetic/ferromagnetic sub-50 nm core multishell coordination nanoparticles have been synthesized in a surfactant-free one-pot multistep procedure with good control over the dispersity (10% standard deviation) and good agreement with the targeted size at each step. The composition and the valence state of each shell have been probed by different techniques that have revealed the predominance of Co(II)-NC-Fe(III) pairs in a series synthesized without alkali while Co(III)-NC-Fe(II) photoswitchable pairs have been successfully obtained in the photoactive coordination nanoparticles by control of Cs(+) insertion. When compared, the photoinduced behavior of the latter compound is in good agreement with that of the model one. Exchange coupling favors a uniform reversal of the magnetization of the heterostructured nanoparticles, with a large magnetization brought by a soft ferromagnetic shell and a large coercivity due to a harder photomagnetic shell. Moreover, a persistent increase of the photoinduced magnetization is observed for the first time up to the ordering temperature (60 K) of the ferromagnetic component because of a unique synergy.< Réduire
Mots clés en italien
Cre-multishell nanoparticles
Cobalt
Nickel
Ferromagnetism
Photomagnetism
Origine
Importé de halUnités de recherche