Nanoparticle-enabled integration of air capture and conversion of CO
Integrating air capture and conversion of CO 2 is key to realizing energy sustainability. However, current integration approaches require high temperature and pressure, making them energy intensive. Here, we demonstrate a nanoparticle (NP) catalysis approach for the hydrogenation of alkyl carbonate,...
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Veröffentlicht in: | Nanoscale 2024-10, Vol.16 (39), p.1862-18628 |
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creator | Guan, Huanqin Kim, Ju Ye Wei, Kecheng Agrawal, Mayank Peterson, Andrew A Sun, Shouheng |
description | Integrating air capture and conversion of CO
2
is key to realizing energy sustainability. However, current integration approaches require high temperature and pressure, making them energy intensive. Here, we demonstrate a nanoparticle (NP) catalysis approach for the hydrogenation of alkyl carbonate, an intermediate obtained from the CO
2
capture process, to formate, achieving one-pot air capture and conversion of CO
2
under ambient conditions. The capture is realized in an ethylene glycol (EG) solution of KOH (EG-KOH) at room temperature, where CO
2
is selectively converted into HO-CH
2
CH
2
-O-COOK (∼100% conversion). This carbonate is then hydrogenated using ammonia borane (under ambient pressure and at 50 °C) to formate (HCOOK) (>90% yield) in the presence of a stable Pd NP catalyst with EG being regenerated. Atomistic simulations suggest that the CO
2
absorption process in the EG-KOH solution is energetically stable, and the catalyst surface provides the reaction site to break the C-O bond in the -O-COOK structure, enabling the hydrogenation of the alkyl carbonate to formate and the regeneration of EG. Our study provides a promising NP-catalysis approach for air capture and conversion of CO
2
into value-added chemicals/fuels under ambient conditions.
This work demonstrates a nanoparticle-enabled integration of air capture and conversion of CO
2
. Ambient CO
2
is captured in a KOH-ethylene glycol solution and then selectively reduced to formate under 50 °C and ambient pressure using Pd NPs. |
doi_str_mv | 10.1039/d4nr02925a |
format | Article |
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2
is key to realizing energy sustainability. However, current integration approaches require high temperature and pressure, making them energy intensive. Here, we demonstrate a nanoparticle (NP) catalysis approach for the hydrogenation of alkyl carbonate, an intermediate obtained from the CO
2
capture process, to formate, achieving one-pot air capture and conversion of CO
2
under ambient conditions. The capture is realized in an ethylene glycol (EG) solution of KOH (EG-KOH) at room temperature, where CO
2
is selectively converted into HO-CH
2
CH
2
-O-COOK (∼100% conversion). This carbonate is then hydrogenated using ammonia borane (under ambient pressure and at 50 °C) to formate (HCOOK) (>90% yield) in the presence of a stable Pd NP catalyst with EG being regenerated. Atomistic simulations suggest that the CO
2
absorption process in the EG-KOH solution is energetically stable, and the catalyst surface provides the reaction site to break the C-O bond in the -O-COOK structure, enabling the hydrogenation of the alkyl carbonate to formate and the regeneration of EG. Our study provides a promising NP-catalysis approach for air capture and conversion of CO
2
into value-added chemicals/fuels under ambient conditions.
This work demonstrates a nanoparticle-enabled integration of air capture and conversion of CO
2
. Ambient CO
2
is captured in a KOH-ethylene glycol solution and then selectively reduced to formate under 50 °C and ambient pressure using Pd NPs.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/d4nr02925a</identifier><ispartof>Nanoscale, 2024-10, Vol.16 (39), p.1862-18628</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Guan, Huanqin</creatorcontrib><creatorcontrib>Kim, Ju Ye</creatorcontrib><creatorcontrib>Wei, Kecheng</creatorcontrib><creatorcontrib>Agrawal, Mayank</creatorcontrib><creatorcontrib>Peterson, Andrew A</creatorcontrib><creatorcontrib>Sun, Shouheng</creatorcontrib><title>Nanoparticle-enabled integration of air capture and conversion of CO</title><title>Nanoscale</title><description>Integrating air capture and conversion of CO
2
is key to realizing energy sustainability. However, current integration approaches require high temperature and pressure, making them energy intensive. Here, we demonstrate a nanoparticle (NP) catalysis approach for the hydrogenation of alkyl carbonate, an intermediate obtained from the CO
2
capture process, to formate, achieving one-pot air capture and conversion of CO
2
under ambient conditions. The capture is realized in an ethylene glycol (EG) solution of KOH (EG-KOH) at room temperature, where CO
2
is selectively converted into HO-CH
2
CH
2
-O-COOK (∼100% conversion). This carbonate is then hydrogenated using ammonia borane (under ambient pressure and at 50 °C) to formate (HCOOK) (>90% yield) in the presence of a stable Pd NP catalyst with EG being regenerated. Atomistic simulations suggest that the CO
2
absorption process in the EG-KOH solution is energetically stable, and the catalyst surface provides the reaction site to break the C-O bond in the -O-COOK structure, enabling the hydrogenation of the alkyl carbonate to formate and the regeneration of EG. Our study provides a promising NP-catalysis approach for air capture and conversion of CO
2
into value-added chemicals/fuels under ambient conditions.
This work demonstrates a nanoparticle-enabled integration of air capture and conversion of CO
2
. Ambient CO
2
is captured in a KOH-ethylene glycol solution and then selectively reduced to formate under 50 °C and ambient pressure using Pd NPs.</description><issn>2040-3364</issn><issn>2040-3372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFjj0LwjAUAIMoWD8WdyF_oPqa1Ernqjjp4l6eSSqRmpSXKPjvXYqOTndwyzG2yGCVgSzXOncEohQbHLBEQA6plFsx_HqRj9kkhDtAUcpCJmx3Quc7pGhVa1Lj8Noaza2L5kYYrXfcNxwtcYVdfJLh6DRX3r0Mhb5W5xkbNdgGM-85ZcvD_lIdUwqq7sg-kN71b03-6x_cJjx4</recordid><startdate>20241010</startdate><enddate>20241010</enddate><creator>Guan, Huanqin</creator><creator>Kim, Ju Ye</creator><creator>Wei, Kecheng</creator><creator>Agrawal, Mayank</creator><creator>Peterson, Andrew A</creator><creator>Sun, Shouheng</creator><scope/></search><sort><creationdate>20241010</creationdate><title>Nanoparticle-enabled integration of air capture and conversion of CO</title><author>Guan, Huanqin ; Kim, Ju Ye ; Wei, Kecheng ; Agrawal, Mayank ; Peterson, Andrew A ; Sun, Shouheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d4nr02925a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guan, Huanqin</creatorcontrib><creatorcontrib>Kim, Ju Ye</creatorcontrib><creatorcontrib>Wei, Kecheng</creatorcontrib><creatorcontrib>Agrawal, Mayank</creatorcontrib><creatorcontrib>Peterson, Andrew A</creatorcontrib><creatorcontrib>Sun, Shouheng</creatorcontrib><jtitle>Nanoscale</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guan, Huanqin</au><au>Kim, Ju Ye</au><au>Wei, Kecheng</au><au>Agrawal, Mayank</au><au>Peterson, Andrew A</au><au>Sun, Shouheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanoparticle-enabled integration of air capture and conversion of CO</atitle><jtitle>Nanoscale</jtitle><date>2024-10-10</date><risdate>2024</risdate><volume>16</volume><issue>39</issue><spage>1862</spage><epage>18628</epage><pages>1862-18628</pages><issn>2040-3364</issn><eissn>2040-3372</eissn><abstract>Integrating air capture and conversion of CO
2
is key to realizing energy sustainability. However, current integration approaches require high temperature and pressure, making them energy intensive. Here, we demonstrate a nanoparticle (NP) catalysis approach for the hydrogenation of alkyl carbonate, an intermediate obtained from the CO
2
capture process, to formate, achieving one-pot air capture and conversion of CO
2
under ambient conditions. The capture is realized in an ethylene glycol (EG) solution of KOH (EG-KOH) at room temperature, where CO
2
is selectively converted into HO-CH
2
CH
2
-O-COOK (∼100% conversion). This carbonate is then hydrogenated using ammonia borane (under ambient pressure and at 50 °C) to formate (HCOOK) (>90% yield) in the presence of a stable Pd NP catalyst with EG being regenerated. Atomistic simulations suggest that the CO
2
absorption process in the EG-KOH solution is energetically stable, and the catalyst surface provides the reaction site to break the C-O bond in the -O-COOK structure, enabling the hydrogenation of the alkyl carbonate to formate and the regeneration of EG. Our study provides a promising NP-catalysis approach for air capture and conversion of CO
2
into value-added chemicals/fuels under ambient conditions.
This work demonstrates a nanoparticle-enabled integration of air capture and conversion of CO
2
. Ambient CO
2
is captured in a KOH-ethylene glycol solution and then selectively reduced to formate under 50 °C and ambient pressure using Pd NPs.</abstract><doi>10.1039/d4nr02925a</doi><tpages>9</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
title | Nanoparticle-enabled integration of air capture and conversion of CO |
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