Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics
Renewed interest in the perovskite ferroelectric barium titanate (BaTiO3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO3 was confi...
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th-cmuir.6653943832-71662014-08-30T03:51:39Z Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics Srisombat L. Ananta S. Singhana B. Lee T.R. Yimnirun R. Renewed interest in the perovskite ferroelectric barium titanate (BaTiO3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO3 was confirmed in Fe3+/Nb 5+-doped BaTiO3 systems. It is well documented that the electronic behavior of BaTiO3 is intimately related to the chemical state of the constituents. However, information regarding the chemical states of the ions of the Fe3+/Nb5+-doped BaTiO3 ceramics is currently unavailable. Consequently, this study describes the chemical state of sintered hybrid Fe3+/Nb5+-doped BaTiO3 ceramics, compared with undoped BaTiO3 ceramics derived from the same processing. Analysis by X-ray photoelectron spectroscopy (XPS) showed that the binding energy of Ti indicates the presence of more than one component of Ti within the doped BaTiO3 ceramics, but only one component of Ti within the undoped BaTiO3 ceramics. Unlike Ti, the XPS spectra indicates that more than one type of barium and oxygen species exist in both undoped and doped BaTiO3 ceramics. © 2012 Elsevier Ltd and Techna Group S.r.l. 2014-08-30T03:51:39Z 2014-08-30T03:51:39Z 2013 Conference Paper 02728842 10.1016/j.ceramint.2012.10.142 CINND http://www.scopus.com/inward/record.url?eid=2-s2.0-84875735154&partnerID=40&md5=e7223c803cdf4ff967898e806e2b0269 http://cmuir.cmu.ac.th/handle/6653943832/7166 English |
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Renewed interest in the perovskite ferroelectric barium titanate (BaTiO3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO3 was confirmed in Fe3+/Nb 5+-doped BaTiO3 systems. It is well documented that the electronic behavior of BaTiO3 is intimately related to the chemical state of the constituents. However, information regarding the chemical states of the ions of the Fe3+/Nb5+-doped BaTiO3 ceramics is currently unavailable. Consequently, this study describes the chemical state of sintered hybrid Fe3+/Nb5+-doped BaTiO3 ceramics, compared with undoped BaTiO3 ceramics derived from the same processing. Analysis by X-ray photoelectron spectroscopy (XPS) showed that the binding energy of Ti indicates the presence of more than one component of Ti within the doped BaTiO3 ceramics, but only one component of Ti within the undoped BaTiO3 ceramics. Unlike Ti, the XPS spectra indicates that more than one type of barium and oxygen species exist in both undoped and doped BaTiO3 ceramics. © 2012 Elsevier Ltd and Techna Group S.r.l. |
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Conference or Workshop Item |
author |
Srisombat L. Ananta S. Singhana B. Lee T.R. Yimnirun R. |
spellingShingle |
Srisombat L. Ananta S. Singhana B. Lee T.R. Yimnirun R. Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
author_facet |
Srisombat L. Ananta S. Singhana B. Lee T.R. Yimnirun R. |
author_sort |
Srisombat L. |
title |
Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
title_short |
Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
title_full |
Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
title_fullStr |
Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
title_full_unstemmed |
Chemical investigation of Fe3+/Nb5+-doped barium titanate ceramics |
title_sort |
chemical investigation of fe3+/nb5+-doped barium titanate ceramics |
publishDate |
2014 |
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http://www.scopus.com/inward/record.url?eid=2-s2.0-84875735154&partnerID=40&md5=e7223c803cdf4ff967898e806e2b0269 http://cmuir.cmu.ac.th/handle/6653943832/7166 |
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