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Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies
Anatase TiO2 nanosheets (TiO2-NS) and nanospindles (TiO2-NSP) have been successfully prepared with F– and glacial acetic acid as structure-directing agents, respectively. The Fe2O3/TiO2-NS and Fe2O3/TiO2-NSP nanocatalysts were prepared by a wet incipient impregnation method with a monolayer amount o...
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Published in: | Journal of physical chemistry. C 2017-03, Vol.121 (9), p.4970-4979 |
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container_title | Journal of physical chemistry. C |
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creator | Liu, Jie Meeprasert, Jittima Namuangruk, Supawadee Zha, Kaiwen Li, Hongrui Huang, Lei Maitarad, Phornphimon Shi, Liyi Zhang, Dengsong |
description | Anatase TiO2 nanosheets (TiO2-NS) and nanospindles (TiO2-NSP) have been successfully prepared with F– and glacial acetic acid as structure-directing agents, respectively. The Fe2O3/TiO2-NS and Fe2O3/TiO2-NSP nanocatalysts were prepared by a wet incipient impregnation method with a monolayer amount of Fe2O3. All the catalysts were employed for the selective catalytic reduction of NO with NH3 (NH3-SCR) in order to understand the morphology-dependent effects. It is interesting that the Fe2O3/TiO2-NS nanocatalyst exhibited better removal efficiency of NO x in the temperature range of 100–450 °C, which was attributed to more oxygen defects and active oxygen, acid sites, as well as adsorbed nitrate species based on Raman spectra, XPS, NH3-TPD, NO+O2-TPD, and in situ DRIFTS. The density functional theory (DFT) method was used to clarify the NO and NH3 adsorption abilities over the catalyst models of Fe2O3/TiO2{001} and Fe2O3/TiO2{101}. The results showed that the NH3 adsorption energy over the TiO2{001} (−2.00 eV) was lower than that over TiO2{101} (−1.21 eV), and the NO adsorption energy over TiO2{001} (−1.62 eV) was also lower than that over TiO2{101} (−0.29 eV), which agreed well with the experimental results that Fe2O3/TiO2-NS achieved higher catalytic activity than Fe2O3/TiO2-NSP for NH3-SCR of NO. In addition, the rapid electron transfer and regeneration of Fe3+ on the {001} facet of Fe2O3/TiO2-NS also promoted the NH3-SCR reaction efficiency. This work paves a way for understanding the facet–activity relationship of Fe2O3/TiO2 nanocatalysts in the NH3-SCR reaction. |
doi_str_mv | 10.1021/acs.jpcc.6b11175 |
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fullrecord | <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_acs_jpcc_6b11175</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c255325744</sourcerecordid><originalsourceid>FETCH-LOGICAL-a192t-314f7e387fd20b1768c577b10c152b4997205e23b55914990130502f5df9c2cc3</originalsourceid><addsrcrecordid>eNo9kMFOwkAQhjdGExG9e5wHENjZ7bLUGwErJIQmUM_NdrsNS5qWsFsNN59B39AnsUXiaeb_D99kPkIekQ6RMhwp7Yb7g9bDcYaIUlyRHoacDWQgxPX_HshbcufcnlLBKfIe-YqUNv7n83uqvX23_gQbUypv68rt7AHqAhIbM7AVRIbFfHROa1XVWnlVnpx3UNRH2JrSdAADs3PvrW5BeaM7UkdZx_Bh_Q7WC_4Mywq21jcw3yyjxIGqcphHCWx9k1vj7slNoUpnHi6zT96il2S2GKzi1-VsuhooDJkfcAwKafhEFjmjGcrxRAspM6QaBcuCMJSMCsN4JkSIbWzfpYKyQuRFqJnWvE-e_ritunRfN8eqvZYiTTuf6blsfaYXn_wXkLtpmw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Liu, Jie ; Meeprasert, Jittima ; Namuangruk, Supawadee ; Zha, Kaiwen ; Li, Hongrui ; Huang, Lei ; Maitarad, Phornphimon ; Shi, Liyi ; Zhang, Dengsong</creator><creatorcontrib>Liu, Jie ; Meeprasert, Jittima ; Namuangruk, Supawadee ; Zha, Kaiwen ; Li, Hongrui ; Huang, Lei ; Maitarad, Phornphimon ; Shi, Liyi ; Zhang, Dengsong</creatorcontrib><description>Anatase TiO2 nanosheets (TiO2-NS) and nanospindles (TiO2-NSP) have been successfully prepared with F– and glacial acetic acid as structure-directing agents, respectively. The Fe2O3/TiO2-NS and Fe2O3/TiO2-NSP nanocatalysts were prepared by a wet incipient impregnation method with a monolayer amount of Fe2O3. All the catalysts were employed for the selective catalytic reduction of NO with NH3 (NH3-SCR) in order to understand the morphology-dependent effects. It is interesting that the Fe2O3/TiO2-NS nanocatalyst exhibited better removal efficiency of NO x in the temperature range of 100–450 °C, which was attributed to more oxygen defects and active oxygen, acid sites, as well as adsorbed nitrate species based on Raman spectra, XPS, NH3-TPD, NO+O2-TPD, and in situ DRIFTS. The density functional theory (DFT) method was used to clarify the NO and NH3 adsorption abilities over the catalyst models of Fe2O3/TiO2{001} and Fe2O3/TiO2{101}. The results showed that the NH3 adsorption energy over the TiO2{001} (−2.00 eV) was lower than that over TiO2{101} (−1.21 eV), and the NO adsorption energy over TiO2{001} (−1.62 eV) was also lower than that over TiO2{101} (−0.29 eV), which agreed well with the experimental results that Fe2O3/TiO2-NS achieved higher catalytic activity than Fe2O3/TiO2-NSP for NH3-SCR of NO. In addition, the rapid electron transfer and regeneration of Fe3+ on the {001} facet of Fe2O3/TiO2-NS also promoted the NH3-SCR reaction efficiency. This work paves a way for understanding the facet–activity relationship of Fe2O3/TiO2 nanocatalysts in the NH3-SCR reaction.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.6b11175</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. C, 2017-03, Vol.121 (9), p.4970-4979</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-4280-0068</orcidid></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>Liu, Jie</creatorcontrib><creatorcontrib>Meeprasert, Jittima</creatorcontrib><creatorcontrib>Namuangruk, Supawadee</creatorcontrib><creatorcontrib>Zha, Kaiwen</creatorcontrib><creatorcontrib>Li, Hongrui</creatorcontrib><creatorcontrib>Huang, Lei</creatorcontrib><creatorcontrib>Maitarad, Phornphimon</creatorcontrib><creatorcontrib>Shi, Liyi</creatorcontrib><creatorcontrib>Zhang, Dengsong</creatorcontrib><title>Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>Anatase TiO2 nanosheets (TiO2-NS) and nanospindles (TiO2-NSP) have been successfully prepared with F– and glacial acetic acid as structure-directing agents, respectively. The Fe2O3/TiO2-NS and Fe2O3/TiO2-NSP nanocatalysts were prepared by a wet incipient impregnation method with a monolayer amount of Fe2O3. All the catalysts were employed for the selective catalytic reduction of NO with NH3 (NH3-SCR) in order to understand the morphology-dependent effects. It is interesting that the Fe2O3/TiO2-NS nanocatalyst exhibited better removal efficiency of NO x in the temperature range of 100–450 °C, which was attributed to more oxygen defects and active oxygen, acid sites, as well as adsorbed nitrate species based on Raman spectra, XPS, NH3-TPD, NO+O2-TPD, and in situ DRIFTS. The density functional theory (DFT) method was used to clarify the NO and NH3 adsorption abilities over the catalyst models of Fe2O3/TiO2{001} and Fe2O3/TiO2{101}. The results showed that the NH3 adsorption energy over the TiO2{001} (−2.00 eV) was lower than that over TiO2{101} (−1.21 eV), and the NO adsorption energy over TiO2{001} (−1.62 eV) was also lower than that over TiO2{101} (−0.29 eV), which agreed well with the experimental results that Fe2O3/TiO2-NS achieved higher catalytic activity than Fe2O3/TiO2-NSP for NH3-SCR of NO. In addition, the rapid electron transfer and regeneration of Fe3+ on the {001} facet of Fe2O3/TiO2-NS also promoted the NH3-SCR reaction efficiency. This work paves a way for understanding the facet–activity relationship of Fe2O3/TiO2 nanocatalysts in the NH3-SCR reaction.</description><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9kMFOwkAQhjdGExG9e5wHENjZ7bLUGwErJIQmUM_NdrsNS5qWsFsNN59B39AnsUXiaeb_D99kPkIekQ6RMhwp7Yb7g9bDcYaIUlyRHoacDWQgxPX_HshbcufcnlLBKfIe-YqUNv7n83uqvX23_gQbUypv68rt7AHqAhIbM7AVRIbFfHROa1XVWnlVnpx3UNRH2JrSdAADs3PvrW5BeaM7UkdZx_Bh_Q7WC_4Mywq21jcw3yyjxIGqcphHCWx9k1vj7slNoUpnHi6zT96il2S2GKzi1-VsuhooDJkfcAwKafhEFjmjGcrxRAspM6QaBcuCMJSMCsN4JkSIbWzfpYKyQuRFqJnWvE-e_ritunRfN8eqvZYiTTuf6blsfaYXn_wXkLtpmw</recordid><startdate>20170309</startdate><enddate>20170309</enddate><creator>Liu, Jie</creator><creator>Meeprasert, Jittima</creator><creator>Namuangruk, Supawadee</creator><creator>Zha, Kaiwen</creator><creator>Li, Hongrui</creator><creator>Huang, Lei</creator><creator>Maitarad, Phornphimon</creator><creator>Shi, Liyi</creator><creator>Zhang, Dengsong</creator><general>American Chemical Society</general><scope/><orcidid>https://orcid.org/0000-0003-4280-0068</orcidid></search><sort><creationdate>20170309</creationdate><title>Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies</title><author>Liu, Jie ; Meeprasert, Jittima ; Namuangruk, Supawadee ; Zha, Kaiwen ; Li, Hongrui ; Huang, Lei ; Maitarad, Phornphimon ; Shi, Liyi ; Zhang, Dengsong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a192t-314f7e387fd20b1768c577b10c152b4997205e23b55914990130502f5df9c2cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jie</creatorcontrib><creatorcontrib>Meeprasert, Jittima</creatorcontrib><creatorcontrib>Namuangruk, Supawadee</creatorcontrib><creatorcontrib>Zha, Kaiwen</creatorcontrib><creatorcontrib>Li, Hongrui</creatorcontrib><creatorcontrib>Huang, Lei</creatorcontrib><creatorcontrib>Maitarad, Phornphimon</creatorcontrib><creatorcontrib>Shi, Liyi</creatorcontrib><creatorcontrib>Zhang, Dengsong</creatorcontrib><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jie</au><au>Meeprasert, Jittima</au><au>Namuangruk, Supawadee</au><au>Zha, Kaiwen</au><au>Li, Hongrui</au><au>Huang, Lei</au><au>Maitarad, Phornphimon</au><au>Shi, Liyi</au><au>Zhang, Dengsong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2017-03-09</date><risdate>2017</risdate><volume>121</volume><issue>9</issue><spage>4970</spage><epage>4979</epage><pages>4970-4979</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Anatase TiO2 nanosheets (TiO2-NS) and nanospindles (TiO2-NSP) have been successfully prepared with F– and glacial acetic acid as structure-directing agents, respectively. The Fe2O3/TiO2-NS and Fe2O3/TiO2-NSP nanocatalysts were prepared by a wet incipient impregnation method with a monolayer amount of Fe2O3. All the catalysts were employed for the selective catalytic reduction of NO with NH3 (NH3-SCR) in order to understand the morphology-dependent effects. It is interesting that the Fe2O3/TiO2-NS nanocatalyst exhibited better removal efficiency of NO x in the temperature range of 100–450 °C, which was attributed to more oxygen defects and active oxygen, acid sites, as well as adsorbed nitrate species based on Raman spectra, XPS, NH3-TPD, NO+O2-TPD, and in situ DRIFTS. The density functional theory (DFT) method was used to clarify the NO and NH3 adsorption abilities over the catalyst models of Fe2O3/TiO2{001} and Fe2O3/TiO2{101}. The results showed that the NH3 adsorption energy over the TiO2{001} (−2.00 eV) was lower than that over TiO2{101} (−1.21 eV), and the NO adsorption energy over TiO2{001} (−1.62 eV) was also lower than that over TiO2{101} (−0.29 eV), which agreed well with the experimental results that Fe2O3/TiO2-NS achieved higher catalytic activity than Fe2O3/TiO2-NSP for NH3-SCR of NO. In addition, the rapid electron transfer and regeneration of Fe3+ on the {001} facet of Fe2O3/TiO2-NS also promoted the NH3-SCR reaction efficiency. This work paves a way for understanding the facet–activity relationship of Fe2O3/TiO2 nanocatalysts in the NH3-SCR reaction.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.6b11175</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4280-0068</orcidid></addata></record> |
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title | Facet–Activity Relationship of TiO2 in Fe2O3/TiO2 Nanocatalysts for Selective Catalytic Reduction of NO with NH3: In Situ DRIFTs and DFT Studies |
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