Loading…

Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates

A two-step tandem electrochemical–thermochemical reaction scheme is demonstrated to convert CO2 into value-added C3 oxygenate molecules: CO2 was electrochemically reduced to ethylene, CO, and H2, followed by the thermochemical hydroformylation reaction to produce 1-propanol and propanal. The CO2 ele...

Full description

Saved in:
Bibliographic Details
Published in:ACS energy letters 2022-09, Vol.7 (9), p.2904-2910
Main Authors: Biswas, Akash N., Xie, Zhenhua, Xia, Rong, Overa, Sean, Jiao, Feng, Chen, Jingguang G.
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 2910
container_issue 9
container_start_page 2904
container_title ACS energy letters
container_volume 7
creator Biswas, Akash N.
Xie, Zhenhua
Xia, Rong
Overa, Sean
Jiao, Feng
Chen, Jingguang G.
description A two-step tandem electrochemical–thermochemical reaction scheme is demonstrated to convert CO2 into value-added C3 oxygenate molecules: CO2 was electrochemically reduced to ethylene, CO, and H2, followed by the thermochemical hydroformylation reaction to produce 1-propanol and propanal. The CO2 electrolyzer was evaluated with Cu catalysts containing different oxidation states and with modifications to the gas diffusion layer hydrophobicity, while the hydroformylation reactor was tested over a Rh1Co3/MCM-41 catalyst. In situ X-ray absorption spectroscopy showed minimal changes to the Cu and Rh catalysts in the electrochemical and thermochemical reactions, respectively. The tandem configuration achieved a total C3 oxygenate product selectivity (on a basis of reduced CO2) of ∼18%, representing over a 4-fold improvement compared to direct electrochemical CO2 conversion to 1-propanol in flow cells. Additionally, the CO2 electrolyzer was scaled to a 25 cm2 device to enhance the C3 oxygenate production rate up to 11.8 μmol min–1 and demonstrate potential scalability of the tandem system.
doi_str_mv 10.1021/acsenergylett.2c01454
format article
fullrecord <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_acsenergylett_2c01454</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a390328686</sourcerecordid><originalsourceid>FETCH-LOGICAL-a127t-bb9fe350180b99fb170530b4c347735d834a003936788c9b0e9f04d957ac90a3</originalsourceid><addsrcrecordid>eNpVkF1KxDAUhYMoOIyzBCEb6HjTJNPkUcr4AwMF7auUJL2dH9oG0ij2zT24Q1diBwdUzsM5nAP3wkfINYMlg5TdGDdgj2E7thjjMnXAhBRnZJZyBYliWp7_yZdkMQwHAGArJSfNyEtp-ho7um7RxeCdiaYd4959fXyWOwzdb0Of0Li49z19djvskDY-0LxIae77NwzDcYme5pwW7-MWexNxuCIXjWkHXJx8Tsq7dZk_JJvi_jG_3SSGpVlMrNUNcglMgdW6sSwDycEKx0WWcVkrLgwA13yVKeW0BdQNiFrLzDgNhs8J-zk7wagO_jX007OKQXUkVP0jVJ0I8W8PpV8R</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Biswas, Akash N. ; Xie, Zhenhua ; Xia, Rong ; Overa, Sean ; Jiao, Feng ; Chen, Jingguang G.</creator><creatorcontrib>Biswas, Akash N. ; Xie, Zhenhua ; Xia, Rong ; Overa, Sean ; Jiao, Feng ; Chen, Jingguang G.</creatorcontrib><description>A two-step tandem electrochemical–thermochemical reaction scheme is demonstrated to convert CO2 into value-added C3 oxygenate molecules: CO2 was electrochemically reduced to ethylene, CO, and H2, followed by the thermochemical hydroformylation reaction to produce 1-propanol and propanal. The CO2 electrolyzer was evaluated with Cu catalysts containing different oxidation states and with modifications to the gas diffusion layer hydrophobicity, while the hydroformylation reactor was tested over a Rh1Co3/MCM-41 catalyst. In situ X-ray absorption spectroscopy showed minimal changes to the Cu and Rh catalysts in the electrochemical and thermochemical reactions, respectively. The tandem configuration achieved a total C3 oxygenate product selectivity (on a basis of reduced CO2) of ∼18%, representing over a 4-fold improvement compared to direct electrochemical CO2 conversion to 1-propanol in flow cells. Additionally, the CO2 electrolyzer was scaled to a 25 cm2 device to enhance the C3 oxygenate production rate up to 11.8 μmol min–1 and demonstrate potential scalability of the tandem system.</description><identifier>ISSN: 2380-8195</identifier><identifier>EISSN: 2380-8195</identifier><identifier>DOI: 10.1021/acsenergylett.2c01454</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS energy letters, 2022-09, Vol.7 (9), p.2904-2910</ispartof><rights>2022 American Chemical Society</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-0105-8805 ; 0000-0002-9592-2635 ; 0000-0002-3335-3203 ; 0000-0003-2076-8116</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Biswas, Akash N.</creatorcontrib><creatorcontrib>Xie, Zhenhua</creatorcontrib><creatorcontrib>Xia, Rong</creatorcontrib><creatorcontrib>Overa, Sean</creatorcontrib><creatorcontrib>Jiao, Feng</creatorcontrib><creatorcontrib>Chen, Jingguang G.</creatorcontrib><title>Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates</title><title>ACS energy letters</title><addtitle>ACS Energy Lett</addtitle><description>A two-step tandem electrochemical–thermochemical reaction scheme is demonstrated to convert CO2 into value-added C3 oxygenate molecules: CO2 was electrochemically reduced to ethylene, CO, and H2, followed by the thermochemical hydroformylation reaction to produce 1-propanol and propanal. The CO2 electrolyzer was evaluated with Cu catalysts containing different oxidation states and with modifications to the gas diffusion layer hydrophobicity, while the hydroformylation reactor was tested over a Rh1Co3/MCM-41 catalyst. In situ X-ray absorption spectroscopy showed minimal changes to the Cu and Rh catalysts in the electrochemical and thermochemical reactions, respectively. The tandem configuration achieved a total C3 oxygenate product selectivity (on a basis of reduced CO2) of ∼18%, representing over a 4-fold improvement compared to direct electrochemical CO2 conversion to 1-propanol in flow cells. Additionally, the CO2 electrolyzer was scaled to a 25 cm2 device to enhance the C3 oxygenate production rate up to 11.8 μmol min–1 and demonstrate potential scalability of the tandem system.</description><issn>2380-8195</issn><issn>2380-8195</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpVkF1KxDAUhYMoOIyzBCEb6HjTJNPkUcr4AwMF7auUJL2dH9oG0ij2zT24Q1diBwdUzsM5nAP3wkfINYMlg5TdGDdgj2E7thjjMnXAhBRnZJZyBYliWp7_yZdkMQwHAGArJSfNyEtp-ho7um7RxeCdiaYd4959fXyWOwzdb0Of0Li49z19djvskDY-0LxIae77NwzDcYme5pwW7-MWexNxuCIXjWkHXJx8Tsq7dZk_JJvi_jG_3SSGpVlMrNUNcglMgdW6sSwDycEKx0WWcVkrLgwA13yVKeW0BdQNiFrLzDgNhs8J-zk7wagO_jX007OKQXUkVP0jVJ0I8W8PpV8R</recordid><startdate>20220909</startdate><enddate>20220909</enddate><creator>Biswas, Akash N.</creator><creator>Xie, Zhenhua</creator><creator>Xia, Rong</creator><creator>Overa, Sean</creator><creator>Jiao, Feng</creator><creator>Chen, Jingguang G.</creator><general>American Chemical Society</general><scope/><orcidid>https://orcid.org/0000-0003-0105-8805</orcidid><orcidid>https://orcid.org/0000-0002-9592-2635</orcidid><orcidid>https://orcid.org/0000-0002-3335-3203</orcidid><orcidid>https://orcid.org/0000-0003-2076-8116</orcidid></search><sort><creationdate>20220909</creationdate><title>Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates</title><author>Biswas, Akash N. ; Xie, Zhenhua ; Xia, Rong ; Overa, Sean ; Jiao, Feng ; Chen, Jingguang G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a127t-bb9fe350180b99fb170530b4c347735d834a003936788c9b0e9f04d957ac90a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Biswas, Akash N.</creatorcontrib><creatorcontrib>Xie, Zhenhua</creatorcontrib><creatorcontrib>Xia, Rong</creatorcontrib><creatorcontrib>Overa, Sean</creatorcontrib><creatorcontrib>Jiao, Feng</creatorcontrib><creatorcontrib>Chen, Jingguang G.</creatorcontrib><jtitle>ACS energy letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Biswas, Akash N.</au><au>Xie, Zhenhua</au><au>Xia, Rong</au><au>Overa, Sean</au><au>Jiao, Feng</au><au>Chen, Jingguang G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates</atitle><jtitle>ACS energy letters</jtitle><addtitle>ACS Energy Lett</addtitle><date>2022-09-09</date><risdate>2022</risdate><volume>7</volume><issue>9</issue><spage>2904</spage><epage>2910</epage><pages>2904-2910</pages><issn>2380-8195</issn><eissn>2380-8195</eissn><abstract>A two-step tandem electrochemical–thermochemical reaction scheme is demonstrated to convert CO2 into value-added C3 oxygenate molecules: CO2 was electrochemically reduced to ethylene, CO, and H2, followed by the thermochemical hydroformylation reaction to produce 1-propanol and propanal. The CO2 electrolyzer was evaluated with Cu catalysts containing different oxidation states and with modifications to the gas diffusion layer hydrophobicity, while the hydroformylation reactor was tested over a Rh1Co3/MCM-41 catalyst. In situ X-ray absorption spectroscopy showed minimal changes to the Cu and Rh catalysts in the electrochemical and thermochemical reactions, respectively. The tandem configuration achieved a total C3 oxygenate product selectivity (on a basis of reduced CO2) of ∼18%, representing over a 4-fold improvement compared to direct electrochemical CO2 conversion to 1-propanol in flow cells. Additionally, the CO2 electrolyzer was scaled to a 25 cm2 device to enhance the C3 oxygenate production rate up to 11.8 μmol min–1 and demonstrate potential scalability of the tandem system.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsenergylett.2c01454</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0105-8805</orcidid><orcidid>https://orcid.org/0000-0002-9592-2635</orcidid><orcidid>https://orcid.org/0000-0002-3335-3203</orcidid><orcidid>https://orcid.org/0000-0003-2076-8116</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2380-8195
ispartof ACS energy letters, 2022-09, Vol.7 (9), p.2904-2910
issn 2380-8195
2380-8195
language eng
recordid cdi_acs_journals_10_1021_acsenergylett_2c01454
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Tandem Electrocatalytic–Thermocatalytic Reaction Scheme for CO2 Conversion to C3 Oxygenates
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T15%3A02%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tandem%20Electrocatalytic%E2%80%93Thermocatalytic%20Reaction%20Scheme%20for%20CO2%20Conversion%20to%20C3%20Oxygenates&rft.jtitle=ACS%20energy%20letters&rft.au=Biswas,%20Akash%20N.&rft.date=2022-09-09&rft.volume=7&rft.issue=9&rft.spage=2904&rft.epage=2910&rft.pages=2904-2910&rft.issn=2380-8195&rft.eissn=2380-8195&rft_id=info:doi/10.1021/acsenergylett.2c01454&rft_dat=%3Cacs%3Ea390328686%3C/acs%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a127t-bb9fe350180b99fb170530b4c347735d834a003936788c9b0e9f04d957ac90a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true