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Toward solar-driven photocatalytic CO2 methanation under continuous flow operation using benchmark MIL-125(Ti)–NH2 supported ruthenium nanoparticles
[Display omitted] •RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active for CO2 methanation.•The photocatalyst is reusable under simulated sunlight irradiation at least for 220 h.•The photocatalyst can operate at least 50 h under continuous flow conditions.•A dual photo-therma...
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Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-10, Vol.445, p.136426, Article 136426 |
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container_title | Chemical engineering journal (Lausanne, Switzerland : 1996) |
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creator | Cabrero-Antonino, María Ferrer, Belén Baldoví, Herme G. Navalón, Sergio |
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•RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active for CO2 methanation.•The photocatalyst is reusable under simulated sunlight irradiation at least for 220 h.•The photocatalyst can operate at least 50 h under continuous flow conditions.•A dual photo-thermal reaction mechanism is proposed.
The production of solar fuels from CO2 is currently attracting increasing interest. Herein we describe the development of a benchmark metal–organic framework (MOF) photocatalyst based on MIL-125(Ti)–NH2 supported ruthenium nanoparticles for solar-driven selective photocatalytic CO2 methanation. The optimized RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active (18.5 mmol g−1 at 22 h) and reusable (10 cycles for 220 h) in the CO2 methanation at 200 °C under batch conditions and simulated sunlight irradiation. The photocatalyst can also be employed for continuous-flow CO2 methanation under visible light irradiation at 200 °C for at least 50 h. Evidence in support of the operation of a dual photo-thermal mechanism that combines a photochemical mechanism based on e-/h+ separation and thermochemical contributions in which the energy of photons produces local heating has been obtained for the photocatalytic CO2 methanation. We are confident that this study will contribute to the development of active MOF-based photocatalysts for solar-driven CO2 methanation under continuous flow operations with industrial interest. |
doi_str_mv | 10.1016/j.cej.2022.136426 |
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•RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active for CO2 methanation.•The photocatalyst is reusable under simulated sunlight irradiation at least for 220 h.•The photocatalyst can operate at least 50 h under continuous flow conditions.•A dual photo-thermal reaction mechanism is proposed.
The production of solar fuels from CO2 is currently attracting increasing interest. Herein we describe the development of a benchmark metal–organic framework (MOF) photocatalyst based on MIL-125(Ti)–NH2 supported ruthenium nanoparticles for solar-driven selective photocatalytic CO2 methanation. The optimized RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active (18.5 mmol g−1 at 22 h) and reusable (10 cycles for 220 h) in the CO2 methanation at 200 °C under batch conditions and simulated sunlight irradiation. The photocatalyst can also be employed for continuous-flow CO2 methanation under visible light irradiation at 200 °C for at least 50 h. Evidence in support of the operation of a dual photo-thermal mechanism that combines a photochemical mechanism based on e-/h+ separation and thermochemical contributions in which the energy of photons produces local heating has been obtained for the photocatalytic CO2 methanation. We are confident that this study will contribute to the development of active MOF-based photocatalysts for solar-driven CO2 methanation under continuous flow operations with industrial interest.</description><identifier>ISSN: 1385-8947</identifier><identifier>EISSN: 1873-3212</identifier><identifier>DOI: 10.1016/j.cej.2022.136426</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Continuous flow operation ; Heterogeneous photocatalysis ; MIL-125(Ti)–NH2 ; Ruthenium nanoparticles ; Simulated sunlight irradiation</subject><ispartof>Chemical engineering journal (Lausanne, Switzerland : 1996), 2022-10, Vol.445, p.136426, Article 136426</ispartof><rights>2022 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c336t-a5f1747da1c3b8647e4d4fef9fb16d80aaabcfbefac790f5292da231d451f3db3</citedby><cites>FETCH-LOGICAL-c336t-a5f1747da1c3b8647e4d4fef9fb16d80aaabcfbefac790f5292da231d451f3db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Cabrero-Antonino, María</creatorcontrib><creatorcontrib>Ferrer, Belén</creatorcontrib><creatorcontrib>Baldoví, Herme G.</creatorcontrib><creatorcontrib>Navalón, Sergio</creatorcontrib><title>Toward solar-driven photocatalytic CO2 methanation under continuous flow operation using benchmark MIL-125(Ti)–NH2 supported ruthenium nanoparticles</title><title>Chemical engineering journal (Lausanne, Switzerland : 1996)</title><description>[Display omitted]
•RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active for CO2 methanation.•The photocatalyst is reusable under simulated sunlight irradiation at least for 220 h.•The photocatalyst can operate at least 50 h under continuous flow conditions.•A dual photo-thermal reaction mechanism is proposed.
The production of solar fuels from CO2 is currently attracting increasing interest. Herein we describe the development of a benchmark metal–organic framework (MOF) photocatalyst based on MIL-125(Ti)–NH2 supported ruthenium nanoparticles for solar-driven selective photocatalytic CO2 methanation. The optimized RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active (18.5 mmol g−1 at 22 h) and reusable (10 cycles for 220 h) in the CO2 methanation at 200 °C under batch conditions and simulated sunlight irradiation. The photocatalyst can also be employed for continuous-flow CO2 methanation under visible light irradiation at 200 °C for at least 50 h. Evidence in support of the operation of a dual photo-thermal mechanism that combines a photochemical mechanism based on e-/h+ separation and thermochemical contributions in which the energy of photons produces local heating has been obtained for the photocatalytic CO2 methanation. We are confident that this study will contribute to the development of active MOF-based photocatalysts for solar-driven CO2 methanation under continuous flow operations with industrial interest.</description><subject>Continuous flow operation</subject><subject>Heterogeneous photocatalysis</subject><subject>MIL-125(Ti)–NH2</subject><subject>Ruthenium nanoparticles</subject><subject>Simulated sunlight irradiation</subject><issn>1385-8947</issn><issn>1873-3212</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OGzEQx1eoSNDAA3DzsRw2-GM_1VMVQUFK4RLO1qw9Jt5u7JXtJcqt71CJB-yTdFE4c5qRRr-Z__yy7IrRJaOsuumXCvslp5wvmagKXp1k56ypRS4441_mXjRl3rRFfZZ9jbGnlFYta8-zt43fQ9Ak-gFCroN9RUfGrU9eQYLhkKwiqydOdpi24CBZ78jkNAaivEvWTX6KxAx-T_yI4WMerXshHTq13UH4TX49rHPGy28be_3vz9_He07iNI4-JNQkTGmLzk474sD5EcJ8cMB4kZ0aGCJeftRF9nx3u1nd5-unnw-rH-tcCVGlHErD6qLWwJTomqqosdCFQdOajlW6oQDQKdOhAVW31JS85Rq4YLoomRG6E4uMHfeq4GMMaOQY7Bz6IBmV72JlL2ex8l2sPIqdme9HBudgrxaDjMrOz6K2AVWS2ttP6P8ZmIZW</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Cabrero-Antonino, María</creator><creator>Ferrer, Belén</creator><creator>Baldoví, Herme G.</creator><creator>Navalón, Sergio</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20221001</creationdate><title>Toward solar-driven photocatalytic CO2 methanation under continuous flow operation using benchmark MIL-125(Ti)–NH2 supported ruthenium nanoparticles</title><author>Cabrero-Antonino, María ; Ferrer, Belén ; Baldoví, Herme G. ; Navalón, Sergio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c336t-a5f1747da1c3b8647e4d4fef9fb16d80aaabcfbefac790f5292da231d451f3db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Continuous flow operation</topic><topic>Heterogeneous photocatalysis</topic><topic>MIL-125(Ti)–NH2</topic><topic>Ruthenium nanoparticles</topic><topic>Simulated sunlight irradiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cabrero-Antonino, María</creatorcontrib><creatorcontrib>Ferrer, Belén</creatorcontrib><creatorcontrib>Baldoví, Herme G.</creatorcontrib><creatorcontrib>Navalón, Sergio</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cabrero-Antonino, María</au><au>Ferrer, Belén</au><au>Baldoví, Herme G.</au><au>Navalón, Sergio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toward solar-driven photocatalytic CO2 methanation under continuous flow operation using benchmark MIL-125(Ti)–NH2 supported ruthenium nanoparticles</atitle><jtitle>Chemical engineering journal (Lausanne, Switzerland : 1996)</jtitle><date>2022-10-01</date><risdate>2022</risdate><volume>445</volume><spage>136426</spage><pages>136426-</pages><artnum>136426</artnum><issn>1385-8947</issn><eissn>1873-3212</eissn><abstract>[Display omitted]
•RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active for CO2 methanation.•The photocatalyst is reusable under simulated sunlight irradiation at least for 220 h.•The photocatalyst can operate at least 50 h under continuous flow conditions.•A dual photo-thermal reaction mechanism is proposed.
The production of solar fuels from CO2 is currently attracting increasing interest. Herein we describe the development of a benchmark metal–organic framework (MOF) photocatalyst based on MIL-125(Ti)–NH2 supported ruthenium nanoparticles for solar-driven selective photocatalytic CO2 methanation. The optimized RuOx(10 wt%; 1.48 nm)@MIL-125(Ti)–NH2 photocatalyst is exceptionally active (18.5 mmol g−1 at 22 h) and reusable (10 cycles for 220 h) in the CO2 methanation at 200 °C under batch conditions and simulated sunlight irradiation. The photocatalyst can also be employed for continuous-flow CO2 methanation under visible light irradiation at 200 °C for at least 50 h. Evidence in support of the operation of a dual photo-thermal mechanism that combines a photochemical mechanism based on e-/h+ separation and thermochemical contributions in which the energy of photons produces local heating has been obtained for the photocatalytic CO2 methanation. We are confident that this study will contribute to the development of active MOF-based photocatalysts for solar-driven CO2 methanation under continuous flow operations with industrial interest.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cej.2022.136426</doi><oa>free_for_read</oa></addata></record> |
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subjects | Continuous flow operation Heterogeneous photocatalysis MIL-125(Ti)–NH2 Ruthenium nanoparticles Simulated sunlight irradiation |
title | Toward solar-driven photocatalytic CO2 methanation under continuous flow operation using benchmark MIL-125(Ti)–NH2 supported ruthenium nanoparticles |
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