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Photoelectrochemical properties of the relaxor Ba(Ti0.90Sc0.05Nb0.05)O3: application to the degradation of amoxicillin under solar light
Polycrystalline sample Ba(Ti 0.9 Sc 0.05 Nb 0.05 )O 3 (BTSN) has been synthesized by solid-state reaction. The effects on the symmetry and dielectric properties of simultaneous cationic substitution of scandium and niobium in the titanium site of BaTiO 3 were investigated. The room-temperature X-ray...
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Published in: | Journal of materials science. Materials in electronics 2018-03, Vol.29 (6), p.5042-5048 |
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creator | Haddadou, N. Bensemma, N. Rekhila, G. Trari, M. Taïbi, K. |
description | Polycrystalline sample Ba(Ti
0.9
Sc
0.05
Nb
0.05
)O
3
(BTSN) has been synthesized by solid-state reaction. The effects on the symmetry and dielectric properties of simultaneous cationic substitution of scandium and niobium in the titanium site of BaTiO
3
were investigated. The room-temperature X-ray diffraction revealed a cubic perovskite phase after sintering at 1350 °C. The dielectric properties in the ranges (80–445 K) and (10
2
–10
6
Hz) were studied. A broad dielectric band anomaly coupled with the shift of dielectric maxima toward higher temperatures with increasing frequency indicates a diffuse phase transition with a relaxor behavior. The parameters of the diffuse phase transition were evaluated from the linear plot of the modified Curie–Weiss law and a good fit to the Vogel–Fülcher relation corroborates the relaxor nature. The relaxor ferroelectric is characterized by a spontaneous polarization which should promote the separation of electron/hole (e
−
/h
+
) pairs and favors the photocatalytic properties in the nanodomains. The electrochemical impedance spectroscopy, measured over the region (1 mH–10
5
Hz) at pH ~ 7, shows the predominance of the bulk contribution. This BTSN ferroelectric ceramic possesses attractive photoelectrochemical properties with an optical gap of 2.54 eV and a flat band potential of 0.45 V
SCE
. As application, the oxide was successfully tested for the photooxydation under solar light of amoxicillin (AMX), a currently used antibiotic. Indeed, the energy band diagram indicates an electron transfer from the conduction band to dissolved oxygen, forming O
2
·
radicals, responsible of the AMX degradation. The AMX concentration was followed by high performance liquid chromatography. A conversion of 92% is recorded in AMX solution (50 mg L
−1
) within 4 h under solar light and the kinetic obeys to a first order model with a rate constant of 7.73 × 10
−3
min
−1
. |
doi_str_mv | 10.1007/s10854-017-8466-1 |
format | article |
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0.9
Sc
0.05
Nb
0.05
)O
3
(BTSN) has been synthesized by solid-state reaction. The effects on the symmetry and dielectric properties of simultaneous cationic substitution of scandium and niobium in the titanium site of BaTiO
3
were investigated. The room-temperature X-ray diffraction revealed a cubic perovskite phase after sintering at 1350 °C. The dielectric properties in the ranges (80–445 K) and (10
2
–10
6
Hz) were studied. A broad dielectric band anomaly coupled with the shift of dielectric maxima toward higher temperatures with increasing frequency indicates a diffuse phase transition with a relaxor behavior. The parameters of the diffuse phase transition were evaluated from the linear plot of the modified Curie–Weiss law and a good fit to the Vogel–Fülcher relation corroborates the relaxor nature. The relaxor ferroelectric is characterized by a spontaneous polarization which should promote the separation of electron/hole (e
−
/h
+
) pairs and favors the photocatalytic properties in the nanodomains. The electrochemical impedance spectroscopy, measured over the region (1 mH–10
5
Hz) at pH ~ 7, shows the predominance of the bulk contribution. This BTSN ferroelectric ceramic possesses attractive photoelectrochemical properties with an optical gap of 2.54 eV and a flat band potential of 0.45 V
SCE
. As application, the oxide was successfully tested for the photooxydation under solar light of amoxicillin (AMX), a currently used antibiotic. Indeed, the energy band diagram indicates an electron transfer from the conduction band to dissolved oxygen, forming O
2
·
radicals, responsible of the AMX degradation. The AMX concentration was followed by high performance liquid chromatography. A conversion of 92% is recorded in AMX solution (50 mg L
−1
) within 4 h under solar light and the kinetic obeys to a first order model with a rate constant of 7.73 × 10
−3
min
−1
.</description><identifier>ISSN: 0957-4522</identifier><identifier>EISSN: 1573-482X</identifier><identifier>DOI: 10.1007/s10854-017-8466-1</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Amoxicillin ; Antibiotics ; Barium titanates ; Characterization and Evaluation of Materials ; Chemical synthesis ; Chemistry and Materials Science ; Conduction bands ; Degradation ; Dielectric properties ; Electrochemical impedance spectroscopy ; Electron transfer ; Ferroelectric materials ; Ferroelectricity ; High performance liquid chromatography ; Materials Science ; Maxima ; Niobium ; Optical and Electronic Materials ; Optical properties ; Oxidation ; Phase transitions ; Scandium ; Substitution reactions ; Titanium</subject><ispartof>Journal of materials science. Materials in electronics, 2018-03, Vol.29 (6), p.5042-5048</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2017</rights><rights>Journal of Materials Science: Materials in Electronics is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2701-255e9a4caabf98d899b5c9a9dfa969616aa7316b295bbd2acc9a3a2fc76b6e493</citedby><cites>FETCH-LOGICAL-c2701-255e9a4caabf98d899b5c9a9dfa969616aa7316b295bbd2acc9a3a2fc76b6e493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Haddadou, N.</creatorcontrib><creatorcontrib>Bensemma, N.</creatorcontrib><creatorcontrib>Rekhila, G.</creatorcontrib><creatorcontrib>Trari, M.</creatorcontrib><creatorcontrib>Taïbi, K.</creatorcontrib><title>Photoelectrochemical properties of the relaxor Ba(Ti0.90Sc0.05Nb0.05)O3: application to the degradation of amoxicillin under solar light</title><title>Journal of materials science. Materials in electronics</title><addtitle>J Mater Sci: Mater Electron</addtitle><description>Polycrystalline sample Ba(Ti
0.9
Sc
0.05
Nb
0.05
)O
3
(BTSN) has been synthesized by solid-state reaction. The effects on the symmetry and dielectric properties of simultaneous cationic substitution of scandium and niobium in the titanium site of BaTiO
3
were investigated. The room-temperature X-ray diffraction revealed a cubic perovskite phase after sintering at 1350 °C. The dielectric properties in the ranges (80–445 K) and (10
2
–10
6
Hz) were studied. A broad dielectric band anomaly coupled with the shift of dielectric maxima toward higher temperatures with increasing frequency indicates a diffuse phase transition with a relaxor behavior. The parameters of the diffuse phase transition were evaluated from the linear plot of the modified Curie–Weiss law and a good fit to the Vogel–Fülcher relation corroborates the relaxor nature. The relaxor ferroelectric is characterized by a spontaneous polarization which should promote the separation of electron/hole (e
−
/h
+
) pairs and favors the photocatalytic properties in the nanodomains. The electrochemical impedance spectroscopy, measured over the region (1 mH–10
5
Hz) at pH ~ 7, shows the predominance of the bulk contribution. This BTSN ferroelectric ceramic possesses attractive photoelectrochemical properties with an optical gap of 2.54 eV and a flat band potential of 0.45 V
SCE
. As application, the oxide was successfully tested for the photooxydation under solar light of amoxicillin (AMX), a currently used antibiotic. Indeed, the energy band diagram indicates an electron transfer from the conduction band to dissolved oxygen, forming O
2
·
radicals, responsible of the AMX degradation. The AMX concentration was followed by high performance liquid chromatography. A conversion of 92% is recorded in AMX solution (50 mg L
−1
) within 4 h under solar light and the kinetic obeys to a first order model with a rate constant of 7.73 × 10
−3
min
−1
.</description><subject>Amoxicillin</subject><subject>Antibiotics</subject><subject>Barium titanates</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemical synthesis</subject><subject>Chemistry and Materials Science</subject><subject>Conduction bands</subject><subject>Degradation</subject><subject>Dielectric properties</subject><subject>Electrochemical impedance spectroscopy</subject><subject>Electron transfer</subject><subject>Ferroelectric materials</subject><subject>Ferroelectricity</subject><subject>High performance liquid chromatography</subject><subject>Materials Science</subject><subject>Maxima</subject><subject>Niobium</subject><subject>Optical and Electronic Materials</subject><subject>Optical properties</subject><subject>Oxidation</subject><subject>Phase transitions</subject><subject>Scandium</subject><subject>Substitution reactions</subject><subject>Titanium</subject><issn>0957-4522</issn><issn>1573-482X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kMFO3DAQhq2KSl1oH4CbpV7KIcvYiZ24N0AUkBBU6lbiZk0cZ9crbxzsrETfoI9db8OBC5cZaeb__tH8hJwyWDKA-jwxaERVAKuLppKyYB_Igom6LKqGPx2RBShRF5Xg_BM5TmkLALIqmwX5-3MTpmC9NVMMZmN3zqCnYwyjjZOziYaeThtLo_X4EiK9xG8rB0sFvwwsQTy0h3r2WH6nOI4-w5MLA53Cf6iz64jdPMo-uAsvzjjv3UD3Q2cjTcFjpN6tN9Nn8rFHn-yX135Cfv-4Xl3dFvePN3dXF_eF4TWwggthFVYGse1V0zVKtcIoVF2PSirJJGJdMtlyJdq242jyskTem1q20laqPCFfZ9_84_Pepklvwz4O-aRmqgHZqBLKrGKzysSQUrS9HqPbYfyjGehD4HoOXOfA9SFwzTLDZyZl7bC28Y3zu9A_sxuEBQ</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Haddadou, N.</creator><creator>Bensemma, N.</creator><creator>Rekhila, G.</creator><creator>Trari, M.</creator><creator>Taïbi, K.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>L7M</scope><scope>P5Z</scope><scope>P62</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>S0W</scope></search><sort><creationdate>20180301</creationdate><title>Photoelectrochemical properties of the relaxor Ba(Ti0.90Sc0.05Nb0.05)O3: application to the degradation of amoxicillin under solar light</title><author>Haddadou, N. ; Bensemma, N. ; Rekhila, G. ; Trari, M. ; Taïbi, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2701-255e9a4caabf98d899b5c9a9dfa969616aa7316b295bbd2acc9a3a2fc76b6e493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amoxicillin</topic><topic>Antibiotics</topic><topic>Barium titanates</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemical synthesis</topic><topic>Chemistry and Materials Science</topic><topic>Conduction bands</topic><topic>Degradation</topic><topic>Dielectric properties</topic><topic>Electrochemical impedance spectroscopy</topic><topic>Electron transfer</topic><topic>Ferroelectric materials</topic><topic>Ferroelectricity</topic><topic>High performance liquid chromatography</topic><topic>Materials Science</topic><topic>Maxima</topic><topic>Niobium</topic><topic>Optical and Electronic Materials</topic><topic>Optical properties</topic><topic>Oxidation</topic><topic>Phase transitions</topic><topic>Scandium</topic><topic>Substitution reactions</topic><topic>Titanium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haddadou, N.</creatorcontrib><creatorcontrib>Bensemma, N.</creatorcontrib><creatorcontrib>Rekhila, G.</creatorcontrib><creatorcontrib>Trari, M.</creatorcontrib><creatorcontrib>Taïbi, K.</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>https://resources.nclive.org/materials</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>DELNET Engineering & Technology Collection</collection><jtitle>Journal of materials science. Materials in electronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haddadou, N.</au><au>Bensemma, N.</au><au>Rekhila, G.</au><au>Trari, M.</au><au>Taïbi, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoelectrochemical properties of the relaxor Ba(Ti0.90Sc0.05Nb0.05)O3: application to the degradation of amoxicillin under solar light</atitle><jtitle>Journal of materials science. Materials in electronics</jtitle><stitle>J Mater Sci: Mater Electron</stitle><date>2018-03-01</date><risdate>2018</risdate><volume>29</volume><issue>6</issue><spage>5042</spage><epage>5048</epage><pages>5042-5048</pages><issn>0957-4522</issn><eissn>1573-482X</eissn><abstract>Polycrystalline sample Ba(Ti
0.9
Sc
0.05
Nb
0.05
)O
3
(BTSN) has been synthesized by solid-state reaction. The effects on the symmetry and dielectric properties of simultaneous cationic substitution of scandium and niobium in the titanium site of BaTiO
3
were investigated. The room-temperature X-ray diffraction revealed a cubic perovskite phase after sintering at 1350 °C. The dielectric properties in the ranges (80–445 K) and (10
2
–10
6
Hz) were studied. A broad dielectric band anomaly coupled with the shift of dielectric maxima toward higher temperatures with increasing frequency indicates a diffuse phase transition with a relaxor behavior. The parameters of the diffuse phase transition were evaluated from the linear plot of the modified Curie–Weiss law and a good fit to the Vogel–Fülcher relation corroborates the relaxor nature. The relaxor ferroelectric is characterized by a spontaneous polarization which should promote the separation of electron/hole (e
−
/h
+
) pairs and favors the photocatalytic properties in the nanodomains. The electrochemical impedance spectroscopy, measured over the region (1 mH–10
5
Hz) at pH ~ 7, shows the predominance of the bulk contribution. This BTSN ferroelectric ceramic possesses attractive photoelectrochemical properties with an optical gap of 2.54 eV and a flat band potential of 0.45 V
SCE
. As application, the oxide was successfully tested for the photooxydation under solar light of amoxicillin (AMX), a currently used antibiotic. Indeed, the energy band diagram indicates an electron transfer from the conduction band to dissolved oxygen, forming O
2
·
radicals, responsible of the AMX degradation. The AMX concentration was followed by high performance liquid chromatography. A conversion of 92% is recorded in AMX solution (50 mg L
−1
) within 4 h under solar light and the kinetic obeys to a first order model with a rate constant of 7.73 × 10
−3
min
−1
.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10854-017-8466-1</doi><tpages>7</tpages></addata></record> |
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subjects | Amoxicillin Antibiotics Barium titanates Characterization and Evaluation of Materials Chemical synthesis Chemistry and Materials Science Conduction bands Degradation Dielectric properties Electrochemical impedance spectroscopy Electron transfer Ferroelectric materials Ferroelectricity High performance liquid chromatography Materials Science Maxima Niobium Optical and Electronic Materials Optical properties Oxidation Phase transitions Scandium Substitution reactions Titanium |
title | Photoelectrochemical properties of the relaxor Ba(Ti0.90Sc0.05Nb0.05)O3: application to the degradation of amoxicillin under solar light |
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