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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
Main Authors: Liu, Jie, Meeprasert, Jittima, Namuangruk, Supawadee, Zha, Kaiwen, Li, Hongrui, Huang, Lei, Maitarad, Phornphimon, Shi, Liyi, Zhang, Dengsong
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container_issue 9
container_start_page 4970
container_title Journal of physical chemistry. C
container_volume 121
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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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. 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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. 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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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