Chemical investigation of Fe 3+/Nb 5+-doped barium titanate ceramics
Renewed interest in the perovskite ferroelectric barium titanate (BaTiO 3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO 3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO 3 was co...
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th-cmuir.6653943832-69592014-08-30T03:51:25Z Chemical investigation of Fe 3+/Nb 5+-doped barium titanate ceramics Srisombat L. Ananta S. Singhana B. Lee T.R. Yimnirun R. Renewed interest in the perovskite ferroelectric barium titanate (BaTiO 3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO 3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO 3 was confirmed in Fe 3+/Nb 5+-doped BaTiO 3 systems. It is well documented that the electronic behavior of BaTiO 3 is intimately related to the chemical state of the constituents. However, information regarding the chemical states of the ions of the Fe 3+/Nb 5+-doped BaTiO 3 ceramics is currently unavailable. Consequently, this study describes the chemical state of sintered hybrid Fe 3+/Nb 5+-doped BaTiO 3 ceramics, compared with undoped BaTiO 3 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 BaTiO 3 ceramics, but only one component of Ti within the undoped BaTiO 3 ceramics. Unlike Ti, the XPS spectra indicates that more than one type of barium and oxygen species exist in both undoped and doped BaTiO 3 ceramics. © 2012 Elsevier Ltd and Techna Group S.r.l. 2014-08-30T03:51:25Z 2014-08-30T03:51:25Z 2012 Article in Press 2728842 10.1016/j.ceramint.2012.10.142 CINND http://www.scopus.com/inward/record.url?eid=2-s2.0-84868226507&partnerID=40&md5=cd48d2829bcd3c26d38e374c5150149e http://cmuir.cmu.ac.th/handle/6653943832/6959 English |
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Renewed interest in the perovskite ferroelectric barium titanate (BaTiO 3) has been driven by the introduction of large recoverable electrostrain in doped BaTiO 3-based materials. Our previous work demonstrated that the potential for high-performance in Pb-free ferroelectrics based on BaTiO 3 was confirmed in Fe 3+/Nb 5+-doped BaTiO 3 systems. It is well documented that the electronic behavior of BaTiO 3 is intimately related to the chemical state of the constituents. However, information regarding the chemical states of the ions of the Fe 3+/Nb 5+-doped BaTiO 3 ceramics is currently unavailable. Consequently, this study describes the chemical state of sintered hybrid Fe 3+/Nb 5+-doped BaTiO 3 ceramics, compared with undoped BaTiO 3 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 BaTiO 3 ceramics, but only one component of Ti within the undoped BaTiO 3 ceramics. Unlike Ti, the XPS spectra indicates that more than one type of barium and oxygen species exist in both undoped and doped BaTiO 3 ceramics. © 2012 Elsevier Ltd and Techna Group S.r.l. |
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Article |
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 Fe 3+/Nb 5+-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 Fe
3+/Nb
5+-doped barium titanate ceramics |
title_short |
Chemical investigation of Fe
3+/Nb
5+-doped barium titanate ceramics |
title_full |
Chemical investigation of Fe
3+/Nb
5+-doped barium titanate ceramics |
title_fullStr |
Chemical investigation of Fe
3+/Nb
5+-doped barium titanate ceramics |
title_full_unstemmed |
Chemical investigation of Fe
3+/Nb
5+-doped barium titanate ceramics |
title_sort |
chemical investigation of fe
3+/nb
5+-doped barium titanate ceramics |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-84868226507&partnerID=40&md5=cd48d2829bcd3c26d38e374c5150149e http://cmuir.cmu.ac.th/handle/6653943832/6959 |
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