Influence of Cs Loading on Pt/m-ZrO2 Water–Gas Shift Catalysts
Certain alkali metals (Na, K) at targeted loadings have been shown in recent decades to significantly promote the LT-WGS reaction. This occurs at alkali doping levels where a redshift in the C-H band of formate occurs, indicating electronic weakening of the bond. The C-H bond breaking of formate is...
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description | Certain alkali metals (Na, K) at targeted loadings have been shown in recent decades to significantly promote the LT-WGS reaction. This occurs at alkali doping levels where a redshift in the C-H band of formate occurs, indicating electronic weakening of the bond. The C-H bond breaking of formate is the proposed rate-limiting step of the formate associative mechanism, lending support to the occurrence of this mechanism in H2-rich environments of the LT-WGS stage of fuel processors. Continuing in this vein of research, 2%Pt/m-ZrO2 was promoted with various levels of Cs in order to explore its influence on the rate of formate intermediate decomposition, as well as that of LT-WGS in a fixed bed reactor. In situ DRIFTS experiments revealed that Cs promoter loadings of 3.87% to 7.22% resulted in significant acceleration of the forward formate decomposition in steam at 130 °C. Of all of the alkali metals tested to date, the redshift in the formate ν(CH) band with the incorporation of Cs was the greatest. XANES difference experiments at the Pt L2 and L3 edges indicated that the electronic effect was not likely due to an enrichment of electronic density on Pt. CO2 TPD experiments revealed that, unlike Na and K promoters, Cs behaves more like Rb in that the decomposition of the second intermediate in LT-WGS, carbonate species, is hindered due to (1) increased basicity of Cs, (2) the tendency of Cs to cover Pt sites that facilitate CO2 decomposition, and (3) the tendency of Cs to increase Pt particle size as shown by EXAFS results, resulting in fewer Pt sites that facilitate CO2 decomposition. As such, the LT-WGS rate was hindered overall and the rate-limiting step shifted to carbonate decomposition (CO2 removal). Like its Rb counterpart, low levels of added Cs (e.g., 0.72%Cs) were found to improve the stability of the catalyst relative to the unpromoted catalyst; the stability comparison was made at similar CO conversion level as well as similar space velocity. |
doi_str_mv | 10.3390/catal11050570 |
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Jeremy ; Jacobs, Gary</creator><creatorcontrib>Rajabi, Zahra ; Martinelli, Michela ; Watson, Caleb D. ; Cronauer, Donald C. ; Kropf, A. Jeremy ; Jacobs, Gary ; Argonne National Lab. (ANL), Argonne, IL (United States)</creatorcontrib><description>Certain alkali metals (Na, K) at targeted loadings have been shown in recent decades to significantly promote the LT-WGS reaction. This occurs at alkali doping levels where a redshift in the C-H band of formate occurs, indicating electronic weakening of the bond. The C-H bond breaking of formate is the proposed rate-limiting step of the formate associative mechanism, lending support to the occurrence of this mechanism in H2-rich environments of the LT-WGS stage of fuel processors. Continuing in this vein of research, 2%Pt/m-ZrO2 was promoted with various levels of Cs in order to explore its influence on the rate of formate intermediate decomposition, as well as that of LT-WGS in a fixed bed reactor. In situ DRIFTS experiments revealed that Cs promoter loadings of 3.87% to 7.22% resulted in significant acceleration of the forward formate decomposition in steam at 130 °C. Of all of the alkali metals tested to date, the redshift in the formate ν(CH) band with the incorporation of Cs was the greatest. XANES difference experiments at the Pt L2 and L3 edges indicated that the electronic effect was not likely due to an enrichment of electronic density on Pt. CO2 TPD experiments revealed that, unlike Na and K promoters, Cs behaves more like Rb in that the decomposition of the second intermediate in LT-WGS, carbonate species, is hindered due to (1) increased basicity of Cs, (2) the tendency of Cs to cover Pt sites that facilitate CO2 decomposition, and (3) the tendency of Cs to increase Pt particle size as shown by EXAFS results, resulting in fewer Pt sites that facilitate CO2 decomposition. As such, the LT-WGS rate was hindered overall and the rate-limiting step shifted to carbonate decomposition (CO2 removal). Like its Rb counterpart, low levels of added Cs (e.g., 0.72%Cs) were found to improve the stability of the catalyst relative to the unpromoted catalyst; the stability comparison was made at similar CO conversion level as well as similar space velocity.</description><identifier>ISSN: 2073-4344</identifier><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal11050570</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acceleration ; Alkali metals ; alkali promotion ; associative mechanism ; Basicity ; By products ; Carbon dioxide ; Catalysts ; Cesium ; cesium (Cs) ; Chemical reactions ; Constraining ; Decomposition ; electronic effect ; Energy ; Equilibrium ; Fixed beds ; formate ; hydrogen ; Hydrogen bonds ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY ; low temperature water-gas shift (LT-WGS) ; Nuclear fuels ; platinum (Pt) ; Red shift ; Rubidium ; Stability ; zirconia (ZrO2) ; Zirconium dioxide</subject><ispartof>Catalysts, 2021-05, Vol.11 (5), p.570</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c331t-b5ffdaf286ef8b7419a16fd81ceccba53fa48e82f8a09aad11cfdc4dc438869f3</citedby><cites>FETCH-LOGICAL-c331t-b5ffdaf286ef8b7419a16fd81ceccba53fa48e82f8a09aad11cfdc4dc438869f3</cites><orcidid>0000-0002-3556-1751 ; 0000000235561751</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.osti.gov/servlets/purl/1829048$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Rajabi, Zahra</creatorcontrib><creatorcontrib>Martinelli, Michela</creatorcontrib><creatorcontrib>Watson, Caleb D.</creatorcontrib><creatorcontrib>Cronauer, Donald C.</creatorcontrib><creatorcontrib>Kropf, A. Jeremy</creatorcontrib><creatorcontrib>Jacobs, Gary</creatorcontrib><creatorcontrib>Argonne National Lab. (ANL), Argonne, IL (United States)</creatorcontrib><title>Influence of Cs Loading on Pt/m-ZrO2 Water–Gas Shift Catalysts</title><title>Catalysts</title><description>Certain alkali metals (Na, K) at targeted loadings have been shown in recent decades to significantly promote the LT-WGS reaction. This occurs at alkali doping levels where a redshift in the C-H band of formate occurs, indicating electronic weakening of the bond. The C-H bond breaking of formate is the proposed rate-limiting step of the formate associative mechanism, lending support to the occurrence of this mechanism in H2-rich environments of the LT-WGS stage of fuel processors. Continuing in this vein of research, 2%Pt/m-ZrO2 was promoted with various levels of Cs in order to explore its influence on the rate of formate intermediate decomposition, as well as that of LT-WGS in a fixed bed reactor. In situ DRIFTS experiments revealed that Cs promoter loadings of 3.87% to 7.22% resulted in significant acceleration of the forward formate decomposition in steam at 130 °C. Of all of the alkali metals tested to date, the redshift in the formate ν(CH) band with the incorporation of Cs was the greatest. XANES difference experiments at the Pt L2 and L3 edges indicated that the electronic effect was not likely due to an enrichment of electronic density on Pt. CO2 TPD experiments revealed that, unlike Na and K promoters, Cs behaves more like Rb in that the decomposition of the second intermediate in LT-WGS, carbonate species, is hindered due to (1) increased basicity of Cs, (2) the tendency of Cs to cover Pt sites that facilitate CO2 decomposition, and (3) the tendency of Cs to increase Pt particle size as shown by EXAFS results, resulting in fewer Pt sites that facilitate CO2 decomposition. As such, the LT-WGS rate was hindered overall and the rate-limiting step shifted to carbonate decomposition (CO2 removal). Like its Rb counterpart, low levels of added Cs (e.g., 0.72%Cs) were found to improve the stability of the catalyst relative to the unpromoted catalyst; the stability comparison was made at similar CO conversion level as well as similar space velocity.</description><subject>Acceleration</subject><subject>Alkali metals</subject><subject>alkali promotion</subject><subject>associative mechanism</subject><subject>Basicity</subject><subject>By products</subject><subject>Carbon dioxide</subject><subject>Catalysts</subject><subject>Cesium</subject><subject>cesium (Cs)</subject><subject>Chemical reactions</subject><subject>Constraining</subject><subject>Decomposition</subject><subject>electronic effect</subject><subject>Energy</subject><subject>Equilibrium</subject><subject>Fixed beds</subject><subject>formate</subject><subject>hydrogen</subject><subject>Hydrogen bonds</subject><subject>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</subject><subject>low temperature water-gas shift (LT-WGS)</subject><subject>Nuclear fuels</subject><subject>platinum (Pt)</subject><subject>Red shift</subject><subject>Rubidium</subject><subject>Stability</subject><subject>zirconia (ZrO2)</subject><subject>Zirconium dioxide</subject><issn>2073-4344</issn><issn>2073-4344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpVkM9KAzEQxoMoWLRH70HPa_O3zd6URWuhUEFF8BKm2Yzd0m5qkh568x18Q5_ELfWgw8DM4cc333yEXHB2LWXJBg4yrDhnmukROyI9wUayUFKp4z_7KemntGRdlVwarnvkZtLiautb52lAWiU6DVA37TsNLX3Mg3XxFmeCvkL28fvzawyJPi0azLTan9ulnM7JCcIq-f7vPCMv93fP1UMxnY0n1e20cFLyXMw1Yg0ozNCjmY8UL4EPsTbceefmoCWCMt4INMBKgJpzh7VTXUtjhiXKM3J50A0pNza5Jnu3cKFtvcuWG1EyZTro6gBtYvjY-pTtMmxj2_myQkshhe7-7qjiQLkYUooe7SY2a4g7y5ndh2n_hSl_ANuuZ2U</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Rajabi, Zahra</creator><creator>Martinelli, Michela</creator><creator>Watson, Caleb D.</creator><creator>Cronauer, Donald C.</creator><creator>Kropf, A. 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Jeremy ; Jacobs, Gary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c331t-b5ffdaf286ef8b7419a16fd81ceccba53fa48e82f8a09aad11cfdc4dc438869f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acceleration</topic><topic>Alkali metals</topic><topic>alkali promotion</topic><topic>associative mechanism</topic><topic>Basicity</topic><topic>By products</topic><topic>Carbon dioxide</topic><topic>Catalysts</topic><topic>Cesium</topic><topic>cesium (Cs)</topic><topic>Chemical reactions</topic><topic>Constraining</topic><topic>Decomposition</topic><topic>electronic effect</topic><topic>Energy</topic><topic>Equilibrium</topic><topic>Fixed beds</topic><topic>formate</topic><topic>hydrogen</topic><topic>Hydrogen bonds</topic><topic>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</topic><topic>low temperature water-gas shift (LT-WGS)</topic><topic>Nuclear fuels</topic><topic>platinum (Pt)</topic><topic>Red shift</topic><topic>Rubidium</topic><topic>Stability</topic><topic>zirconia (ZrO2)</topic><topic>Zirconium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajabi, Zahra</creatorcontrib><creatorcontrib>Martinelli, Michela</creatorcontrib><creatorcontrib>Watson, Caleb D.</creatorcontrib><creatorcontrib>Cronauer, Donald C.</creatorcontrib><creatorcontrib>Kropf, A. 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Jeremy</au><au>Jacobs, Gary</au><aucorp>Argonne National Lab. (ANL), Argonne, IL (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Cs Loading on Pt/m-ZrO2 Water–Gas Shift Catalysts</atitle><jtitle>Catalysts</jtitle><date>2021-05-01</date><risdate>2021</risdate><volume>11</volume><issue>5</issue><spage>570</spage><pages>570-</pages><issn>2073-4344</issn><eissn>2073-4344</eissn><abstract>Certain alkali metals (Na, K) at targeted loadings have been shown in recent decades to significantly promote the LT-WGS reaction. This occurs at alkali doping levels where a redshift in the C-H band of formate occurs, indicating electronic weakening of the bond. The C-H bond breaking of formate is the proposed rate-limiting step of the formate associative mechanism, lending support to the occurrence of this mechanism in H2-rich environments of the LT-WGS stage of fuel processors. Continuing in this vein of research, 2%Pt/m-ZrO2 was promoted with various levels of Cs in order to explore its influence on the rate of formate intermediate decomposition, as well as that of LT-WGS in a fixed bed reactor. In situ DRIFTS experiments revealed that Cs promoter loadings of 3.87% to 7.22% resulted in significant acceleration of the forward formate decomposition in steam at 130 °C. Of all of the alkali metals tested to date, the redshift in the formate ν(CH) band with the incorporation of Cs was the greatest. XANES difference experiments at the Pt L2 and L3 edges indicated that the electronic effect was not likely due to an enrichment of electronic density on Pt. CO2 TPD experiments revealed that, unlike Na and K promoters, Cs behaves more like Rb in that the decomposition of the second intermediate in LT-WGS, carbonate species, is hindered due to (1) increased basicity of Cs, (2) the tendency of Cs to cover Pt sites that facilitate CO2 decomposition, and (3) the tendency of Cs to increase Pt particle size as shown by EXAFS results, resulting in fewer Pt sites that facilitate CO2 decomposition. As such, the LT-WGS rate was hindered overall and the rate-limiting step shifted to carbonate decomposition (CO2 removal). Like its Rb counterpart, low levels of added Cs (e.g., 0.72%Cs) were found to improve the stability of the catalyst relative to the unpromoted catalyst; the stability comparison was made at similar CO conversion level as well as similar space velocity.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/catal11050570</doi><orcidid>https://orcid.org/0000-0002-3556-1751</orcidid><orcidid>https://orcid.org/0000000235561751</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acceleration Alkali metals alkali promotion associative mechanism Basicity By products Carbon dioxide Catalysts Cesium cesium (Cs) Chemical reactions Constraining Decomposition electronic effect Energy Equilibrium Fixed beds formate hydrogen Hydrogen bonds INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY low temperature water-gas shift (LT-WGS) Nuclear fuels platinum (Pt) Red shift Rubidium Stability zirconia (ZrO2) Zirconium dioxide |
title | Influence of Cs Loading on Pt/m-ZrO2 Water–Gas Shift Catalysts |
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