Synthesis, photocatalytic activity, and photogenerated hydroxyl radicals of monodisperse colloidal ZnO nanospheres

•Spherical ZnO nanoparticles were synthesized via a two-stage solution method.•Calcination temperature influenced particle structure and photocatalytic activity.•ZnO particles calcined at 400°C exhibited the highest photocatalytic activity.•Specific properties facilitated the photocatalytic activity...

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Veröffentlicht in:Applied surface science 2015-12, Vol.357, p.1928-1938
Hauptverfasser: Yang, Chong, Li, Qingsong, Tang, Limei, Xin, Kun, Bai, Ailing, Yu, Yingmin
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container_issue
container_start_page 1928
container_title Applied surface science
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creator Yang, Chong
Li, Qingsong
Tang, Limei
Xin, Kun
Bai, Ailing
Yu, Yingmin
description •Spherical ZnO nanoparticles were synthesized via a two-stage solution method.•Calcination temperature influenced particle structure and photocatalytic activity.•ZnO particles calcined at 400°C exhibited the highest photocatalytic activity.•Specific properties facilitated the photocatalytic activity of ZnO nanoparticles.•Hydroxyl radicals were the main active oxygen species in the photocatalysis. In the present study, monodisperse colloidal zinc oxide (ZnO) nanospheres were successfully synthesized via a newly developed two-stage solution method followed by facile calcination at various temperatures. The effects of calcination temperature on the structure, morphology, and optical properties as well as the photocatalytic activity of the as-made ZnO samples were investigated systematically by Fourier transform infrared spectrometry, X-ray diffraction, field emission scanning electron microscopy, nitrogen adsorption/desorption isotherms, diffuse reflectance UV–visible spectroscopy (DRS), photoluminescence, and related photocatalytic activity tests. The thermal decomposition was analyzed by thermogravimetric analysis. The crystallinity was found to gradually increase with increasing calcination temperature, whereas the decrease in the Brunauer–Emmett–Teller specific surface area of the samples with calcination may be ascribed to the increased particle size. The DRS results provided clear evidence for the decrease in band gap energy of ZnO samples with an increase in calcination temperature. The photoluminescence spectra demonstrated the calcination-dependent emission features, especially the UV emission intensity. In particular, the ZnO product calcined at 400°C exhibited the highest photocatalytic activity, degrading methylene blue by almost 99.1% in 70min, which is ascribed to the large specific surface area and pore volume, high electron–hole pair separation efficient, and great redox potential of the obtained ZnO nanoparticles. In addition, the production of photogenerated hydroxyl radicals (•OH) was consistent with the methylene blue degradation efficiency over the as-made ZnO nanoparticles. Using isopropanol as a hydroxyl radical scavenger, •OH was determined to be the main active oxygen species in the photocatalytic process. A possible mechanism of photodegradation under UV light irradiation also is proposed.
doi_str_mv 10.1016/j.apsusc.2015.09.140
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In the present study, monodisperse colloidal zinc oxide (ZnO) nanospheres were successfully synthesized via a newly developed two-stage solution method followed by facile calcination at various temperatures. The effects of calcination temperature on the structure, morphology, and optical properties as well as the photocatalytic activity of the as-made ZnO samples were investigated systematically by Fourier transform infrared spectrometry, X-ray diffraction, field emission scanning electron microscopy, nitrogen adsorption/desorption isotherms, diffuse reflectance UV–visible spectroscopy (DRS), photoluminescence, and related photocatalytic activity tests. The thermal decomposition was analyzed by thermogravimetric analysis. The crystallinity was found to gradually increase with increasing calcination temperature, whereas the decrease in the Brunauer–Emmett–Teller specific surface area of the samples with calcination may be ascribed to the increased particle size. The DRS results provided clear evidence for the decrease in band gap energy of ZnO samples with an increase in calcination temperature. The photoluminescence spectra demonstrated the calcination-dependent emission features, especially the UV emission intensity. In particular, the ZnO product calcined at 400°C exhibited the highest photocatalytic activity, degrading methylene blue by almost 99.1% in 70min, which is ascribed to the large specific surface area and pore volume, high electron–hole pair separation efficient, and great redox potential of the obtained ZnO nanoparticles. In addition, the production of photogenerated hydroxyl radicals (•OH) was consistent with the methylene blue degradation efficiency over the as-made ZnO nanoparticles. Using isopropanol as a hydroxyl radical scavenger, •OH was determined to be the main active oxygen species in the photocatalytic process. 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In the present study, monodisperse colloidal zinc oxide (ZnO) nanospheres were successfully synthesized via a newly developed two-stage solution method followed by facile calcination at various temperatures. The effects of calcination temperature on the structure, morphology, and optical properties as well as the photocatalytic activity of the as-made ZnO samples were investigated systematically by Fourier transform infrared spectrometry, X-ray diffraction, field emission scanning electron microscopy, nitrogen adsorption/desorption isotherms, diffuse reflectance UV–visible spectroscopy (DRS), photoluminescence, and related photocatalytic activity tests. The thermal decomposition was analyzed by thermogravimetric analysis. The crystallinity was found to gradually increase with increasing calcination temperature, whereas the decrease in the Brunauer–Emmett–Teller specific surface area of the samples with calcination may be ascribed to the increased particle size. The DRS results provided clear evidence for the decrease in band gap energy of ZnO samples with an increase in calcination temperature. The photoluminescence spectra demonstrated the calcination-dependent emission features, especially the UV emission intensity. In particular, the ZnO product calcined at 400°C exhibited the highest photocatalytic activity, degrading methylene blue by almost 99.1% in 70min, which is ascribed to the large specific surface area and pore volume, high electron–hole pair separation efficient, and great redox potential of the obtained ZnO nanoparticles. In addition, the production of photogenerated hydroxyl radicals (•OH) was consistent with the methylene blue degradation efficiency over the as-made ZnO nanoparticles. Using isopropanol as a hydroxyl radical scavenger, •OH was determined to be the main active oxygen species in the photocatalytic process. A possible mechanism of photodegradation under UV light irradiation also is proposed.</description><subject>Calcination</subject><subject>Calcination temperature</subject><subject>Colloids</subject><subject>Emission</subject><subject>Hydroxyl radicals</subject><subject>Methylene blue</subject><subject>Photocatalysis</subject><subject>Photoluminescence</subject><subject>Zinc oxide</subject><subject>ZnO nanospheres</subject><issn>0169-4332</issn><issn>1873-5584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kD1v2zAURYmiBeq6_QcdOGawFFKivpYAhZGkAQx4aLN0IWi-p5qGTKp8dBD9-8hQ5k5vuPdc4B3GvkuRSyHr21NuRrqQzQshq1x0uVTiA1vJtimzqmrVR7aaa12myrL4zL4QnYSQxZyuWPw1-XREcrTh4zGkYE0yw5Sc5cYm9-LStOHGwxL-RY_RJAR-nCCG12ng0YCzZiAeen4OPoCjESMht2EYggMz8D9-z73xgcYjRqSv7FM_A_jt_a7Z88P97-3PbLd_fNr-2GW2bOqUldJ2fW_7qm-V6aBAKVXV1CC6QsFBKSgaBGnqGrqyPrSdwQOCsk1lLEgBWK7ZzbI7xvDvgpT02ZHFYTAew4W0bNpaVpUU5VxVS9XGQBSx12N0ZxMnLYW-KtYnvSjWV8VadHpWPGN3C4bzGy8Ooybr0FsEF9EmDcH9f-ANfdSLEg</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Yang, Chong</creator><creator>Li, Qingsong</creator><creator>Tang, Limei</creator><creator>Xin, Kun</creator><creator>Bai, Ailing</creator><creator>Yu, Yingmin</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-1425-8822</orcidid></search><sort><creationdate>20151201</creationdate><title>Synthesis, photocatalytic activity, and photogenerated hydroxyl radicals of monodisperse colloidal ZnO nanospheres</title><author>Yang, Chong ; Li, Qingsong ; Tang, Limei ; Xin, Kun ; Bai, Ailing ; Yu, Yingmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-31c9ffcf5f84a9d2e114576d0924db44d27ed1a66d936b89aebed4c75acd10de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Calcination</topic><topic>Calcination temperature</topic><topic>Colloids</topic><topic>Emission</topic><topic>Hydroxyl radicals</topic><topic>Methylene blue</topic><topic>Photocatalysis</topic><topic>Photoluminescence</topic><topic>Zinc oxide</topic><topic>ZnO nanospheres</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Chong</creatorcontrib><creatorcontrib>Li, Qingsong</creatorcontrib><creatorcontrib>Tang, Limei</creatorcontrib><creatorcontrib>Xin, Kun</creatorcontrib><creatorcontrib>Bai, Ailing</creatorcontrib><creatorcontrib>Yu, Yingmin</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied surface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Chong</au><au>Li, Qingsong</au><au>Tang, Limei</au><au>Xin, Kun</au><au>Bai, Ailing</au><au>Yu, Yingmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, photocatalytic activity, and photogenerated hydroxyl radicals of monodisperse colloidal ZnO nanospheres</atitle><jtitle>Applied surface science</jtitle><date>2015-12-01</date><risdate>2015</risdate><volume>357</volume><spage>1928</spage><epage>1938</epage><pages>1928-1938</pages><issn>0169-4332</issn><eissn>1873-5584</eissn><abstract>•Spherical ZnO nanoparticles were synthesized via a two-stage solution method.•Calcination temperature influenced particle structure and photocatalytic activity.•ZnO particles calcined at 400°C exhibited the highest photocatalytic activity.•Specific properties facilitated the photocatalytic activity of ZnO nanoparticles.•Hydroxyl radicals were the main active oxygen species in the photocatalysis. 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The DRS results provided clear evidence for the decrease in band gap energy of ZnO samples with an increase in calcination temperature. The photoluminescence spectra demonstrated the calcination-dependent emission features, especially the UV emission intensity. In particular, the ZnO product calcined at 400°C exhibited the highest photocatalytic activity, degrading methylene blue by almost 99.1% in 70min, which is ascribed to the large specific surface area and pore volume, high electron–hole pair separation efficient, and great redox potential of the obtained ZnO nanoparticles. In addition, the production of photogenerated hydroxyl radicals (•OH) was consistent with the methylene blue degradation efficiency over the as-made ZnO nanoparticles. Using isopropanol as a hydroxyl radical scavenger, •OH was determined to be the main active oxygen species in the photocatalytic process. 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subjects Calcination
Calcination temperature
Colloids
Emission
Hydroxyl radicals
Methylene blue
Photocatalysis
Photoluminescence
Zinc oxide
ZnO nanospheres
title Synthesis, photocatalytic activity, and photogenerated hydroxyl radicals of monodisperse colloidal ZnO nanospheres
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