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Enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructure for dye degradation
The novel UV active photocatalysts of (1 − x)CdWO4–xBaTiO3 (where x = 10, 30, 50 and 70 wt%) heterostructures were synthesized using the hydrothermal technique. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-V...
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Published in: | New journal of chemistry 2021-11, Vol.45 (42), p.19723-19732 |
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creator | Sai Sushma, S P Swarupa, G Nagesh, T Pola, Someshwar Rajitha, P B Vijaya Kumar Upender, G |
description | The novel UV active photocatalysts of (1 − x)CdWO4–xBaTiO3 (where x = 10, 30, 50 and 70 wt%) heterostructures were synthesized using the hydrothermal technique. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), Fourier transform infrared (FT-IR) spectroscopy, and photoluminescence (PL) techniques. The photocatalytic activities of BaTiO3, CdWO4 along with all CdWO4/BaTiO3 heterostructures were evaluated for the degradation of methylene blue (MB) dye in an aqueous solution under UV irradiation and it was found that the CdWO4/BaTiO3 (70 : 30 wt%) heterostructure exhibited the highest photocatalytic activity within 45 minutes compared to BaTiO3 and CdWO4. The scavenger tests confirmed that OH·, O2·− and h+ radicals were the main species for the MB degradation. The calculated redox potentials of both BaTiO3, CdWO4 semiconductors indicated that the charge transfer between these two is responsible for the enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructures. Accordingly, the possible mechanisms of the separation of photo-induced electron–hole pairs and charge transfer and also the generation of radicals for MB degradation under UV irradiation were proposed in detail. Our findings clearly suggest that the integration of ferroelectric BaTiO3 with semiconducting CdWO4 could be an effective way to expedite MB dye degradation. |
doi_str_mv | 10.1039/d1nj01556g |
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The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), Fourier transform infrared (FT-IR) spectroscopy, and photoluminescence (PL) techniques. The photocatalytic activities of BaTiO3, CdWO4 along with all CdWO4/BaTiO3 heterostructures were evaluated for the degradation of methylene blue (MB) dye in an aqueous solution under UV irradiation and it was found that the CdWO4/BaTiO3 (70 : 30 wt%) heterostructure exhibited the highest photocatalytic activity within 45 minutes compared to BaTiO3 and CdWO4. The scavenger tests confirmed that OH·, O2·− and h+ radicals were the main species for the MB degradation. The calculated redox potentials of both BaTiO3, CdWO4 semiconductors indicated that the charge transfer between these two is responsible for the enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructures. Accordingly, the possible mechanisms of the separation of photo-induced electron–hole pairs and charge transfer and also the generation of radicals for MB degradation under UV irradiation were proposed in detail. Our findings clearly suggest that the integration of ferroelectric BaTiO3 with semiconducting CdWO4 could be an effective way to expedite MB dye degradation.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d1nj01556g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Aqueous solutions ; Barium titanates ; Catalytic activity ; Charge transfer ; Degradation ; Dyes ; Ferroelectricity ; Fourier transforms ; Heterostructures ; Infrared spectroscopy ; Irradiation ; Methylene blue ; Photocatalysis ; Photoelectrons ; Photoluminescence ; Spectrum analysis ; Ultraviolet radiation ; X ray photoelectron spectroscopy</subject><ispartof>New journal of chemistry, 2021-11, Vol.45 (42), p.19723-19732</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Sai Sushma, S P</creatorcontrib><creatorcontrib>Swarupa, G</creatorcontrib><creatorcontrib>Nagesh, T</creatorcontrib><creatorcontrib>Pola, Someshwar</creatorcontrib><creatorcontrib>Rajitha, P</creatorcontrib><creatorcontrib>B Vijaya Kumar</creatorcontrib><creatorcontrib>Upender, G</creatorcontrib><title>Enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructure for dye degradation</title><title>New journal of chemistry</title><description>The novel UV active photocatalysts of (1 − x)CdWO4–xBaTiO3 (where x = 10, 30, 50 and 70 wt%) heterostructures were synthesized using the hydrothermal technique. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), Fourier transform infrared (FT-IR) spectroscopy, and photoluminescence (PL) techniques. The photocatalytic activities of BaTiO3, CdWO4 along with all CdWO4/BaTiO3 heterostructures were evaluated for the degradation of methylene blue (MB) dye in an aqueous solution under UV irradiation and it was found that the CdWO4/BaTiO3 (70 : 30 wt%) heterostructure exhibited the highest photocatalytic activity within 45 minutes compared to BaTiO3 and CdWO4. The scavenger tests confirmed that OH·, O2·− and h+ radicals were the main species for the MB degradation. The calculated redox potentials of both BaTiO3, CdWO4 semiconductors indicated that the charge transfer between these two is responsible for the enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructures. Accordingly, the possible mechanisms of the separation of photo-induced electron–hole pairs and charge transfer and also the generation of radicals for MB degradation under UV irradiation were proposed in detail. Our findings clearly suggest that the integration of ferroelectric BaTiO3 with semiconducting CdWO4 could be an effective way to expedite MB dye degradation.</description><subject>Aqueous solutions</subject><subject>Barium titanates</subject><subject>Catalytic activity</subject><subject>Charge transfer</subject><subject>Degradation</subject><subject>Dyes</subject><subject>Ferroelectricity</subject><subject>Fourier transforms</subject><subject>Heterostructures</subject><subject>Infrared spectroscopy</subject><subject>Irradiation</subject><subject>Methylene blue</subject><subject>Photocatalysis</subject><subject>Photoelectrons</subject><subject>Photoluminescence</subject><subject>Spectrum analysis</subject><subject>Ultraviolet radiation</subject><subject>X ray photoelectron spectroscopy</subject><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNotj09LwzAYh4MoOKcXP0HAc9375m9z1DKnMNhl4nFkSbq1jKamqdBvb0FPv-f0PPwIeUR4RuBm5bFrAaVUpyuyQK5MYZjC65lRiAKkULfkbhhaAEStcEH26-5sOxc87c8xR2ezvUy5cdS63Pw0eaKxppX_2onVq903O07PIYcUh5xGl8cUaB0T9VOgPpyS9TY3sbsnN7W9DOHhf5fk8229r96L7W7zUb1six6R50LVzFsuHWiwkgcnoTQhGMmOJeqj1UeQCrRGXXLmSjTCC8BSKC1rJpQv-ZI8_Xn7FL_HMORDG8fUzckDk4YDm08z_gstU1Cv</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Sai Sushma, S P</creator><creator>Swarupa, G</creator><creator>Nagesh, T</creator><creator>Pola, Someshwar</creator><creator>Rajitha, P</creator><creator>B Vijaya Kumar</creator><creator>Upender, G</creator><general>Royal Society of Chemistry</general><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H9R</scope><scope>JG9</scope><scope>KA0</scope></search><sort><creationdate>20211101</creationdate><title>Enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructure for dye degradation</title><author>Sai Sushma, S P ; Swarupa, G ; Nagesh, T ; Pola, Someshwar ; Rajitha, P ; B Vijaya Kumar ; Upender, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p113t-6f2da35c070a53ec5089ee952b817ba7b05607717832c8194d40184675f246d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aqueous solutions</topic><topic>Barium titanates</topic><topic>Catalytic activity</topic><topic>Charge transfer</topic><topic>Degradation</topic><topic>Dyes</topic><topic>Ferroelectricity</topic><topic>Fourier transforms</topic><topic>Heterostructures</topic><topic>Infrared spectroscopy</topic><topic>Irradiation</topic><topic>Methylene blue</topic><topic>Photocatalysis</topic><topic>Photoelectrons</topic><topic>Photoluminescence</topic><topic>Spectrum analysis</topic><topic>Ultraviolet radiation</topic><topic>X ray photoelectron spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sai Sushma, S P</creatorcontrib><creatorcontrib>Swarupa, G</creatorcontrib><creatorcontrib>Nagesh, T</creatorcontrib><creatorcontrib>Pola, Someshwar</creatorcontrib><creatorcontrib>Rajitha, P</creatorcontrib><creatorcontrib>B Vijaya Kumar</creatorcontrib><creatorcontrib>Upender, G</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Illustrata: Natural Sciences</collection><collection>Materials Research Database</collection><collection>ProQuest Illustrata: Technology Collection</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sai Sushma, S P</au><au>Swarupa, G</au><au>Nagesh, T</au><au>Pola, Someshwar</au><au>Rajitha, P</au><au>B Vijaya Kumar</au><au>Upender, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructure for dye degradation</atitle><jtitle>New journal of chemistry</jtitle><date>2021-11-01</date><risdate>2021</risdate><volume>45</volume><issue>42</issue><spage>19723</spage><epage>19732</epage><pages>19723-19732</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>The novel UV active photocatalysts of (1 − x)CdWO4–xBaTiO3 (where x = 10, 30, 50 and 70 wt%) heterostructures were synthesized using the hydrothermal technique. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), Fourier transform infrared (FT-IR) spectroscopy, and photoluminescence (PL) techniques. The photocatalytic activities of BaTiO3, CdWO4 along with all CdWO4/BaTiO3 heterostructures were evaluated for the degradation of methylene blue (MB) dye in an aqueous solution under UV irradiation and it was found that the CdWO4/BaTiO3 (70 : 30 wt%) heterostructure exhibited the highest photocatalytic activity within 45 minutes compared to BaTiO3 and CdWO4. The scavenger tests confirmed that OH·, O2·− and h+ radicals were the main species for the MB degradation. The calculated redox potentials of both BaTiO3, CdWO4 semiconductors indicated that the charge transfer between these two is responsible for the enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructures. Accordingly, the possible mechanisms of the separation of photo-induced electron–hole pairs and charge transfer and also the generation of radicals for MB degradation under UV irradiation were proposed in detail. Our findings clearly suggest that the integration of ferroelectric BaTiO3 with semiconducting CdWO4 could be an effective way to expedite MB dye degradation.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1nj01556g</doi><tpages>10</tpages></addata></record> |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Aqueous solutions Barium titanates Catalytic activity Charge transfer Degradation Dyes Ferroelectricity Fourier transforms Heterostructures Infrared spectroscopy Irradiation Methylene blue Photocatalysis Photoelectrons Photoluminescence Spectrum analysis Ultraviolet radiation X ray photoelectron spectroscopy |
title | Enhanced photocatalytic activity of CdWO4/BaTiO3 heterostructure for dye degradation |
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