Visible-Light-Induced Reversible Photomagnetism in Rubidium Manganese Hexacyanoferrate

The photoreversibility of a photoinduced phase transition was investigated in a rubidium manganese hexacyanoferrate, Rb0.88Mn[Fe(CN)6]0.96·0.5H2O. The present material shows a charge-transfer phase transition from the MnII−FeIII [high-temperature (HT)] phase to the MnIII−FeII [low-temperature (LT)]...

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Veröffentlicht in:Chemistry of materials 2008-01, Vol.20 (2), p.423-428
Hauptverfasser: Tokoro, Hiroko, Matsuda, Tomoyuki, Nuida, Tomohiro, Moritomo, Yutaka, Ohoyama, Kenji, Dangui, Edgard Davy Loutete, Boukheddaden, Kamel, Ohkoshi, Shin-ichi
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Sprache:eng
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Zusammenfassung:The photoreversibility of a photoinduced phase transition was investigated in a rubidium manganese hexacyanoferrate, Rb0.88Mn[Fe(CN)6]0.96·0.5H2O. The present material shows a charge-transfer phase transition from the MnII−FeIII [high-temperature (HT)] phase to the MnIII−FeII [low-temperature (LT)] phase, and the LT phase shows ferromagnetism. Spectroscopic ellipsometry measurements of the dielectric constant suggest that the optical transitions in the LT and HT phases are a metal-to-metal charge transfer (FeII → MnIII) band at 420–540 nm and a ligand-to-metal charge transfer (CN– → FeIII) band of [FeIII(CN)6] at 410 nm, respectively. By irradiation with 532 nm light, the LT phase is transmitted to the photoinduced (PI) phase, which has a valence state similar to that of the HT phase, and photodemagnetization is observed. In contrast, irradiating the PI phase with 410 ± 30 nm light causes the reverse phase transition. Neutron powder diffraction measurement of an analogue compound, Rb0.58Mn[Fe(CN)6]0.86·2.3H2O, which does not show a charge-transfer phase transition and maintains the MnII−FeIII phase at a very low temperature, confirms that the PI phase is an antiferromagnet. Hence, the present visible-light-induced reversible photomagnetic effect is due to optical switching between the ferromagnetic LT phase and the antiferromagnetic PI phase.
ISSN:0897-4756
1520-5002
DOI:10.1021/cm701873s