標題: Effect of geometry on the magnetic properties of CoFe2O4-PbTiO3 multiferroic composites
作者: Wang, B. Y.
Wang, H. T.
Singh, Shashi B.
Shao, Y. C.
Wang, Y. F.
Chuang, C. H.
Yeh, P. H.
Chiou, J. W.
Pao, C. W.
Tsai, H. M.
Lin, H. J.
Lee, J. F.
Tsai, C. Y.
Hsieh, W. F.
Tsai, M. -H.
Pong, W. F.
光電工程學系
Department of Photonics
公開日期: 2013
摘要: In this study, X-ray absorption near-edge structure (XANES), extended X-ray absorption fine structure (EXAFS), X-ray magnetic circular dichroism (XMCD) and element-and site-specific magnetic hysteresis (ESMH) are used to elucidate the effect of geometry (0-3- and 2-2-type) on the magnetic properties of CoFe2O4-PbTiO3 (CFO-PTO) multiferroic composites by comparison with those of the reference CFO and PTO powders. Magnetic Co ions in CFO have been confirmed to be located at both the tetrahedral (A)- and octahedral (B)-sites. CFO retains its mixed-spinel structure as verified by the EXAFS, XMCD and ESMH measurements. ESMH measurements further demonstrate that the magnetic moments of Co2+ and Fe3+/Fe2+ cations at both the A-and B-sites in the composites are smaller than those of the CFO powder. The reduction of the magnetic moments in the 2-2-type composite was larger than that in the 0-3-type composite. The reduction of the magnetic moments in the composites was attributable to the formation of anti-phase boundaries owing to the compressive strain in CFO, which is the largest strain in the 2-2-type composite. Based on the Ti L-3,L-2-edge XMCD measurements of the CFO-PTO composites, no induced magnetic moment was observed at the Ti sites in the PTO matrix, excluding the possibility that the Ti ions in the PTO matrix affect the magnetic properties of these CFO-PTO composites.
URI: http://hdl.handle.net/11536/21957
http://dx.doi.org/10.1039/c3ra00104k
ISSN: 2046-2069
DOI: 10.1039/c3ra00104k
期刊: RSC ADVANCES
Volume: 3
Issue: 21
起始頁: 7884
結束頁: 7893
Appears in Collections:Articles


Files in This Item:

  1. 000318634000036.pdf

If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.