Materials with combined ferroelectric and ferromagnetic properties or magneto-electric coupling effects are promising candidates for information technology, photosensoring, and device fabrication. Preparation and characterization of multiferroic materials in which ferroelectricity and ferromagnetism coexist attracted much interest in research for functionalized materials and devices. They present a possibility to electrically control magnetic memory devices and, conversely, magnetically manipulate electric devices. In this work we considered Fe3O4 magnetic nanoparticles with and without a protective SiO2/TiO2 double-layer coating embedded into the carbazole-based, namely, polyepoxypropylcarbazole (PEPC) thin (500 nm) film. Optical characterization of the PEPC films was performed using light irradiation in the UV/VIS and NIR ranges. A shift in the optical absorption edge toward a higher wavelength region of the spectrum took place for all irradiated samples: the polymer film, as well as for the samples with Fe3O4 and Fe3O4/SiO2/TiO2 nanoparticles inside of the polymer matrix. We suggest that changes in the UV/VIS/NIR spectra took place as a function of the degree of structural changes and stabilizing of the atomic matrix, as well as due to change in the values of the refractive index following irradiation, calculated from the spectral data. In such a way photo-structural modifications induced by the UV irradiation and the implantation of the magnetic nanoparticles make these materials perspective for optical recording media. We conclude, therefore, that Fe3O4 and Fe3O4/SiO2/TiO2 nanoparticles considerably affect the optical properties of the PEPC thin film, and result in the enhancement of the photodarkening effect following the UV irradiation.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.