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Single-Atom Ce-Modified α‑Fe2O3 for Selective Catalytic Reduction of NO with NH3
A single-atom Ce-modified α-Fe2O3 catalyst (Fe0.93Ce0.07O x catalyst with 7% atomic percentage of Ce) was synthesized by a citric acid-assisted sol–gel method, which exhibited excellent performance for selective catalytic reduction of NO x with NH3 (NH3-SCR) over a wide operating temperature window....
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Published in: | Environmental science & technology 2022-07, Vol.56 (14), p.10442-10453 |
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creator | Chen, Wei Yang, Shan Liu, Hao Huang, Fang Shao, Qinghao Liu, Lichen Sun, Jingfang Sun, Chuanzhi Chen, Dezhan Dong, Lin |
description | A single-atom Ce-modified α-Fe2O3 catalyst (Fe0.93Ce0.07O x catalyst with 7% atomic percentage of Ce) was synthesized by a citric acid-assisted sol–gel method, which exhibited excellent performance for selective catalytic reduction of NO x with NH3 (NH3-SCR) over a wide operating temperature window. Remarkably, it maintained ∼93% NO conversion efficiency for 168 h in the presence of 200 ppm SO2 and 5 vol % H2O at 250 °C. The structural characterizations suggested that the introduction of Ce leads to the generation of local Fe–O–Ce sites in the FeO x matrix. Furthermore, it is critical to maintain the atomic dispersion of the Ce species to maximize the amounts of Fe–O–Ce sites in the Ce-doped FeO x catalyst. The formation of CeO2 nanoparticles due to a high doping amount of Ce species leads to a decline in catalytic performance, indicating a size-dependent catalytic behavior. Density functional theory (DFT) calculation results indicate that the formation of oxygen vacancies in the Fe–O–Ce sites is more favorable than that in the Fe–O–Fe sites in the Ce-free α-Fe2O3 catalyst. The Fe–O–Ce sites can promote the oxidation of NO to NO2 on the Fe0.93Ce0.07O x catalyst and further facilitate the reduction of NO x by NH3. In addition, the decomposition of NH4HSO4 can occur at lower temperatures on the Fe0.93Ce0.07O x catalyst containing atomically dispersed Ce species than on the α-Fe2O3 reference catalyst, resulting in the good SO2/H2O resistance ability in the NH3-SCR reaction. |
doi_str_mv | 10.1021/acs.est.2c02916 |
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Remarkably, it maintained ∼93% NO conversion efficiency for 168 h in the presence of 200 ppm SO2 and 5 vol % H2O at 250 °C. The structural characterizations suggested that the introduction of Ce leads to the generation of local Fe–O–Ce sites in the FeO x matrix. Furthermore, it is critical to maintain the atomic dispersion of the Ce species to maximize the amounts of Fe–O–Ce sites in the Ce-doped FeO x catalyst. The formation of CeO2 nanoparticles due to a high doping amount of Ce species leads to a decline in catalytic performance, indicating a size-dependent catalytic behavior. Density functional theory (DFT) calculation results indicate that the formation of oxygen vacancies in the Fe–O–Ce sites is more favorable than that in the Fe–O–Fe sites in the Ce-free α-Fe2O3 catalyst. The Fe–O–Ce sites can promote the oxidation of NO to NO2 on the Fe0.93Ce0.07O x catalyst and further facilitate the reduction of NO x by NH3. In addition, the decomposition of NH4HSO4 can occur at lower temperatures on the Fe0.93Ce0.07O x catalyst containing atomically dispersed Ce species than on the α-Fe2O3 reference catalyst, resulting in the good SO2/H2O resistance ability in the NH3-SCR reaction.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.2c02916</identifier><language>eng</language><publisher>Easton: American Chemical Society</publisher><subject>Ammonia ; Catalysts ; Cerium oxides ; Chemical reduction ; Citric acid ; Density functional theory ; Dispersion ; Ferric oxide ; Low temperature ; Nanoparticles ; Nitrogen dioxide ; Operating temperature ; Oxidation ; Selective catalytic reduction ; Sol-gel processes ; Species ; Sulfur dioxide ; Treatment and Resource Recovery</subject><ispartof>Environmental science & technology, 2022-07, Vol.56 (14), p.10442-10453</ispartof><rights>2022 American Chemical Society</rights><rights>Copyright American Chemical Society Jul 19, 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-3744-9800 ; 0000-0002-8393-6669 ; 0000-0003-1963-4874 ; 0000-0001-6849-7269 ; 0000-0003-4801-7111 ; 0000-0001-5067-0481</orcidid></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>Chen, Wei</creatorcontrib><creatorcontrib>Yang, Shan</creatorcontrib><creatorcontrib>Liu, Hao</creatorcontrib><creatorcontrib>Huang, Fang</creatorcontrib><creatorcontrib>Shao, Qinghao</creatorcontrib><creatorcontrib>Liu, Lichen</creatorcontrib><creatorcontrib>Sun, Jingfang</creatorcontrib><creatorcontrib>Sun, Chuanzhi</creatorcontrib><creatorcontrib>Chen, Dezhan</creatorcontrib><creatorcontrib>Dong, Lin</creatorcontrib><title>Single-Atom Ce-Modified α‑Fe2O3 for Selective Catalytic Reduction of NO with NH3</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>A single-atom Ce-modified α-Fe2O3 catalyst (Fe0.93Ce0.07O x catalyst with 7% atomic percentage of Ce) was synthesized by a citric acid-assisted sol–gel method, which exhibited excellent performance for selective catalytic reduction of NO x with NH3 (NH3-SCR) over a wide operating temperature window. Remarkably, it maintained ∼93% NO conversion efficiency for 168 h in the presence of 200 ppm SO2 and 5 vol % H2O at 250 °C. The structural characterizations suggested that the introduction of Ce leads to the generation of local Fe–O–Ce sites in the FeO x matrix. Furthermore, it is critical to maintain the atomic dispersion of the Ce species to maximize the amounts of Fe–O–Ce sites in the Ce-doped FeO x catalyst. The formation of CeO2 nanoparticles due to a high doping amount of Ce species leads to a decline in catalytic performance, indicating a size-dependent catalytic behavior. Density functional theory (DFT) calculation results indicate that the formation of oxygen vacancies in the Fe–O–Ce sites is more favorable than that in the Fe–O–Fe sites in the Ce-free α-Fe2O3 catalyst. The Fe–O–Ce sites can promote the oxidation of NO to NO2 on the Fe0.93Ce0.07O x catalyst and further facilitate the reduction of NO x by NH3. In addition, the decomposition of NH4HSO4 can occur at lower temperatures on the Fe0.93Ce0.07O x catalyst containing atomically dispersed Ce species than on the α-Fe2O3 reference catalyst, resulting in the good SO2/H2O resistance ability in the NH3-SCR reaction.</description><subject>Ammonia</subject><subject>Catalysts</subject><subject>Cerium oxides</subject><subject>Chemical reduction</subject><subject>Citric acid</subject><subject>Density functional theory</subject><subject>Dispersion</subject><subject>Ferric oxide</subject><subject>Low temperature</subject><subject>Nanoparticles</subject><subject>Nitrogen dioxide</subject><subject>Operating temperature</subject><subject>Oxidation</subject><subject>Selective catalytic reduction</subject><subject>Sol-gel processes</subject><subject>Species</subject><subject>Sulfur dioxide</subject><subject>Treatment and Resource Recovery</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkM9Kw0AQhxdRsFbPXhe8CJI6s5v9dyzBWqG2YBW8hU2y0ZQ0q01i8eYr-Ci-iA_hk5jSguBp4Mf3G2Y-Qk4RBggML21aD1zdDFgKzKDcIz0UDAKhBe6THgDywHD5eEiO6noBAIyD7pH5vKieShcMG7-kkQtufVbkhcvo99fPx-fIsRmnuV_RuStd2hRvjka2seV7U6T0zmVtl_mK-pxOZ3RdNM90OubH5CC3Ze1OdrNPHkZX99E4mMyub6LhJLCoWROEMsyUQWesNgITgSpnXGYpE2A0S7gKtQbFhAxVooQGJjJjOOo81BZcgrxPzrd7X1b-te1-j5dFnbqytJXzbR0zqRFCKY3q0LN_6MK3q6q7rqMMUwaA84662FKdyz8AId4IjjfhprkTzH8BTSdsxg</recordid><startdate>20220719</startdate><enddate>20220719</enddate><creator>Chen, Wei</creator><creator>Yang, Shan</creator><creator>Liu, Hao</creator><creator>Huang, Fang</creator><creator>Shao, Qinghao</creator><creator>Liu, Lichen</creator><creator>Sun, Jingfang</creator><creator>Sun, Chuanzhi</creator><creator>Chen, Dezhan</creator><creator>Dong, Lin</creator><general>American Chemical Society</general><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3744-9800</orcidid><orcidid>https://orcid.org/0000-0002-8393-6669</orcidid><orcidid>https://orcid.org/0000-0003-1963-4874</orcidid><orcidid>https://orcid.org/0000-0001-6849-7269</orcidid><orcidid>https://orcid.org/0000-0003-4801-7111</orcidid><orcidid>https://orcid.org/0000-0001-5067-0481</orcidid></search><sort><creationdate>20220719</creationdate><title>Single-Atom Ce-Modified α‑Fe2O3 for Selective Catalytic Reduction of NO with NH3</title><author>Chen, Wei ; Yang, Shan ; Liu, Hao ; Huang, Fang ; Shao, Qinghao ; Liu, Lichen ; Sun, Jingfang ; Sun, Chuanzhi ; Chen, Dezhan ; Dong, Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a182t-464d791e9a8951b517f236dc250982b374880725647b758025d99318f48a0eb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Ammonia</topic><topic>Catalysts</topic><topic>Cerium oxides</topic><topic>Chemical reduction</topic><topic>Citric acid</topic><topic>Density functional theory</topic><topic>Dispersion</topic><topic>Ferric oxide</topic><topic>Low temperature</topic><topic>Nanoparticles</topic><topic>Nitrogen dioxide</topic><topic>Operating temperature</topic><topic>Oxidation</topic><topic>Selective catalytic reduction</topic><topic>Sol-gel processes</topic><topic>Species</topic><topic>Sulfur dioxide</topic><topic>Treatment and Resource Recovery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Wei</creatorcontrib><creatorcontrib>Yang, Shan</creatorcontrib><creatorcontrib>Liu, Hao</creatorcontrib><creatorcontrib>Huang, Fang</creatorcontrib><creatorcontrib>Shao, Qinghao</creatorcontrib><creatorcontrib>Liu, Lichen</creatorcontrib><creatorcontrib>Sun, Jingfang</creatorcontrib><creatorcontrib>Sun, Chuanzhi</creatorcontrib><creatorcontrib>Chen, Dezhan</creatorcontrib><creatorcontrib>Dong, Lin</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Wei</au><au>Yang, Shan</au><au>Liu, Hao</au><au>Huang, Fang</au><au>Shao, Qinghao</au><au>Liu, Lichen</au><au>Sun, Jingfang</au><au>Sun, Chuanzhi</au><au>Chen, Dezhan</au><au>Dong, Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-Atom Ce-Modified α‑Fe2O3 for Selective Catalytic Reduction of NO with NH3</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2022-07-19</date><risdate>2022</risdate><volume>56</volume><issue>14</issue><spage>10442</spage><epage>10453</epage><pages>10442-10453</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><abstract>A single-atom Ce-modified α-Fe2O3 catalyst (Fe0.93Ce0.07O x catalyst with 7% atomic percentage of Ce) was synthesized by a citric acid-assisted sol–gel method, which exhibited excellent performance for selective catalytic reduction of NO x with NH3 (NH3-SCR) over a wide operating temperature window. Remarkably, it maintained ∼93% NO conversion efficiency for 168 h in the presence of 200 ppm SO2 and 5 vol % H2O at 250 °C. The structural characterizations suggested that the introduction of Ce leads to the generation of local Fe–O–Ce sites in the FeO x matrix. Furthermore, it is critical to maintain the atomic dispersion of the Ce species to maximize the amounts of Fe–O–Ce sites in the Ce-doped FeO x catalyst. The formation of CeO2 nanoparticles due to a high doping amount of Ce species leads to a decline in catalytic performance, indicating a size-dependent catalytic behavior. Density functional theory (DFT) calculation results indicate that the formation of oxygen vacancies in the Fe–O–Ce sites is more favorable than that in the Fe–O–Fe sites in the Ce-free α-Fe2O3 catalyst. The Fe–O–Ce sites can promote the oxidation of NO to NO2 on the Fe0.93Ce0.07O x catalyst and further facilitate the reduction of NO x by NH3. In addition, the decomposition of NH4HSO4 can occur at lower temperatures on the Fe0.93Ce0.07O x catalyst containing atomically dispersed Ce species than on the α-Fe2O3 reference catalyst, resulting in the good SO2/H2O resistance ability in the NH3-SCR reaction.</abstract><cop>Easton</cop><pub>American Chemical Society</pub><doi>10.1021/acs.est.2c02916</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-3744-9800</orcidid><orcidid>https://orcid.org/0000-0002-8393-6669</orcidid><orcidid>https://orcid.org/0000-0003-1963-4874</orcidid><orcidid>https://orcid.org/0000-0001-6849-7269</orcidid><orcidid>https://orcid.org/0000-0003-4801-7111</orcidid><orcidid>https://orcid.org/0000-0001-5067-0481</orcidid></addata></record> |
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subjects | Ammonia Catalysts Cerium oxides Chemical reduction Citric acid Density functional theory Dispersion Ferric oxide Low temperature Nanoparticles Nitrogen dioxide Operating temperature Oxidation Selective catalytic reduction Sol-gel processes Species Sulfur dioxide Treatment and Resource Recovery |
title | Single-Atom Ce-Modified α‑Fe2O3 for Selective Catalytic Reduction of NO with NH3 |
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