Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond

The development of highly efficient electrocatalysts for complete oxidation of ethylene glycol (EG) in direct EG fuel cells is of decisive importance to hold higher energy efficiency. Despite some achievements, their progress, especially electrocatalytic selectivity to complete oxidated C1 products,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie International Edition 2024-04, Vol.63 (15), p.e202400281-n/a
Hauptverfasser: Lv, Hao, Mao, Yumeng, Yao, Huiqin, Ma, Huazhong, Han, Chenyu, Yang, Yao‐Yue, Qiao, Zhen‐An, Liu, Ben
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 15
container_start_page e202400281
container_title Angewandte Chemie International Edition
container_volume 63
creator Lv, Hao
Mao, Yumeng
Yao, Huiqin
Ma, Huazhong
Han, Chenyu
Yang, Yao‐Yue
Qiao, Zhen‐An
Liu, Ben
description The development of highly efficient electrocatalysts for complete oxidation of ethylene glycol (EG) in direct EG fuel cells is of decisive importance to hold higher energy efficiency. Despite some achievements, their progress, especially electrocatalytic selectivity to complete oxidated C1 products, is remarkably slower than expected. In this work, we developed a facile aqueous synthesis of Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) as high‐performance electrocatalyst for promoting oxidation cleavage of C−C bond in alkaline EG oxidation reaction (EGOR) electrocatalysis. The synthesis relied on precise reduction/co‐nucleation and epitaxial growth of Ir, Cu and Pd precursors with cetyltrimethylammonium chloride as the mesopore‐forming surfactant and extra Br− as the facet‐selective agent under ambient conditions. The products featured concave nanotetrahedron morphology enclosed by well‐defined (111) facets, single‐crystalline and mesoporous structure radiated from the center, and uniform elemental composition without any phase separation. Ir‐CuPd SMTs disclosed remarkably enhanced electrocatalytic activity and excellent stability as well as superior selectivity of C1 products for alkaline EGOR electrocatalysis. Detailed mechanism studies demonstrated that performance improvement came from structural and compositional synergies, which kinetically accelerated transports of electrons/reactants within active sites of penetrated mesopores and facilitated oxidation cleavage of high‐energy‐barrier C−C bond of EG for desired C1 products. More interestingly, Ir‐CuPd SMTs performed well in coupled electrocatalysis of anode EGOR and cathode nitrate reduction, highlighting its high potential as bifunctional electrocatalyst in various applications. Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) were facilely prepared through an aqueous surfactant‐templating epitaxial growth strategy. With mesoporous channels and multi‐compositions, Ir‐CuPd SMTs delivered remarkable C−C bond cleavage of electrocatalytic ethylene glycol oxidation (EGOR) to C1 products. The Ir‐CuPd SMTs performed perfectly in coupled electrocatalysis of EGOR and nitrate reduction.
doi_str_mv 10.1002/anie.202400281
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2925006784</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2925006784</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3731-e2c65aab9006c56d8236819d22335797efd19d933696096b56d09628d2dfaf553</originalsourceid><addsrcrecordid>eNqFkT9v1DAYhy0Eou3ByogssbDk8J-L47CVEMpJpUUqzJYvftNz5bMPOylk68iIGPl4_ST4dKVILEyvX_vx89r6IfSMkjklhL3S3sKcEbbIjaQP0CEtGS14VfGHeb3gvKhkSQ_QUUpXO0QS8RgdcMl5LSk9RL-W8fbmx9uwBYOb8aPBF9ZfOsh7TZzSoJ2zHvAHSGEbYhgTPtM-DDBEvQYTg0-4DxG3w3pykMETN3XB4fNv1ujBBo9bB90QQ6ezako2vcatX2vf5XEXsDuz14AbB_paXwIOPW5uv_9s8JvgzRP0qNcuwdO7OkOf37WfmvfF6fnJsjk-LTpecVoA60Sp9aomRHSlMJJxIWltGOO8rOoKepO7mnNRC1KLVUZyYdIw0-u-LPkMvdx7tzF8GSENamNTB85pD_nHitWszO5KLjL64h_0KozR59cpThgVXLI8dobme6qLIaUIvdpGu9FxUpSoXWpql5q6Ty1feH6nHVcbMPf4n5gyUO-Br9bB9B-dOj5btn_lvwHkN6ct</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3021638222</pqid></control><display><type>article</type><title>Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond</title><source>Wiley Journals</source><creator>Lv, Hao ; Mao, Yumeng ; Yao, Huiqin ; Ma, Huazhong ; Han, Chenyu ; Yang, Yao‐Yue ; Qiao, Zhen‐An ; Liu, Ben</creator><creatorcontrib>Lv, Hao ; Mao, Yumeng ; Yao, Huiqin ; Ma, Huazhong ; Han, Chenyu ; Yang, Yao‐Yue ; Qiao, Zhen‐An ; Liu, Ben</creatorcontrib><description>The development of highly efficient electrocatalysts for complete oxidation of ethylene glycol (EG) in direct EG fuel cells is of decisive importance to hold higher energy efficiency. Despite some achievements, their progress, especially electrocatalytic selectivity to complete oxidated C1 products, is remarkably slower than expected. In this work, we developed a facile aqueous synthesis of Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) as high‐performance electrocatalyst for promoting oxidation cleavage of C−C bond in alkaline EG oxidation reaction (EGOR) electrocatalysis. The synthesis relied on precise reduction/co‐nucleation and epitaxial growth of Ir, Cu and Pd precursors with cetyltrimethylammonium chloride as the mesopore‐forming surfactant and extra Br− as the facet‐selective agent under ambient conditions. The products featured concave nanotetrahedron morphology enclosed by well‐defined (111) facets, single‐crystalline and mesoporous structure radiated from the center, and uniform elemental composition without any phase separation. Ir‐CuPd SMTs disclosed remarkably enhanced electrocatalytic activity and excellent stability as well as superior selectivity of C1 products for alkaline EGOR electrocatalysis. Detailed mechanism studies demonstrated that performance improvement came from structural and compositional synergies, which kinetically accelerated transports of electrons/reactants within active sites of penetrated mesopores and facilitated oxidation cleavage of high‐energy‐barrier C−C bond of EG for desired C1 products. More interestingly, Ir‐CuPd SMTs performed well in coupled electrocatalysis of anode EGOR and cathode nitrate reduction, highlighting its high potential as bifunctional electrocatalyst in various applications. Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) were facilely prepared through an aqueous surfactant‐templating epitaxial growth strategy. With mesoporous channels and multi‐compositions, Ir‐CuPd SMTs delivered remarkable C−C bond cleavage of electrocatalytic ethylene glycol oxidation (EGOR) to C1 products. The Ir‐CuPd SMTs performed perfectly in coupled electrocatalysis of EGOR and nitrate reduction.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202400281</identifier><identifier>PMID: 38339811</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Catalysis ; Chemical composition ; Chemical synthesis ; Cleavage ; C−C bond cleavage ; Electrocatalysis ; Electrocatalysts ; electrochemistry ; Energy efficiency ; Epitaxial growth ; Ethylene glycol ; Fuel cells ; mesoporous metals ; nanoparticles ; Nitrate reduction ; Nucleation ; Oxidation ; Phase separation ; Reduction ; Selectivity ; single crystals</subject><ispartof>Angewandte Chemie International Edition, 2024-04, Vol.63 (15), p.e202400281-n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><rights>2024 Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3731-e2c65aab9006c56d8236819d22335797efd19d933696096b56d09628d2dfaf553</citedby><cites>FETCH-LOGICAL-c3731-e2c65aab9006c56d8236819d22335797efd19d933696096b56d09628d2dfaf553</cites><orcidid>0000-0001-6064-9360</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202400281$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202400281$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38339811$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lv, Hao</creatorcontrib><creatorcontrib>Mao, Yumeng</creatorcontrib><creatorcontrib>Yao, Huiqin</creatorcontrib><creatorcontrib>Ma, Huazhong</creatorcontrib><creatorcontrib>Han, Chenyu</creatorcontrib><creatorcontrib>Yang, Yao‐Yue</creatorcontrib><creatorcontrib>Qiao, Zhen‐An</creatorcontrib><creatorcontrib>Liu, Ben</creatorcontrib><title>Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>The development of highly efficient electrocatalysts for complete oxidation of ethylene glycol (EG) in direct EG fuel cells is of decisive importance to hold higher energy efficiency. Despite some achievements, their progress, especially electrocatalytic selectivity to complete oxidated C1 products, is remarkably slower than expected. In this work, we developed a facile aqueous synthesis of Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) as high‐performance electrocatalyst for promoting oxidation cleavage of C−C bond in alkaline EG oxidation reaction (EGOR) electrocatalysis. The synthesis relied on precise reduction/co‐nucleation and epitaxial growth of Ir, Cu and Pd precursors with cetyltrimethylammonium chloride as the mesopore‐forming surfactant and extra Br− as the facet‐selective agent under ambient conditions. The products featured concave nanotetrahedron morphology enclosed by well‐defined (111) facets, single‐crystalline and mesoporous structure radiated from the center, and uniform elemental composition without any phase separation. Ir‐CuPd SMTs disclosed remarkably enhanced electrocatalytic activity and excellent stability as well as superior selectivity of C1 products for alkaline EGOR electrocatalysis. Detailed mechanism studies demonstrated that performance improvement came from structural and compositional synergies, which kinetically accelerated transports of electrons/reactants within active sites of penetrated mesopores and facilitated oxidation cleavage of high‐energy‐barrier C−C bond of EG for desired C1 products. More interestingly, Ir‐CuPd SMTs performed well in coupled electrocatalysis of anode EGOR and cathode nitrate reduction, highlighting its high potential as bifunctional electrocatalyst in various applications. Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) were facilely prepared through an aqueous surfactant‐templating epitaxial growth strategy. With mesoporous channels and multi‐compositions, Ir‐CuPd SMTs delivered remarkable C−C bond cleavage of electrocatalytic ethylene glycol oxidation (EGOR) to C1 products. The Ir‐CuPd SMTs performed perfectly in coupled electrocatalysis of EGOR and nitrate reduction.</description><subject>Catalysis</subject><subject>Chemical composition</subject><subject>Chemical synthesis</subject><subject>Cleavage</subject><subject>C−C bond cleavage</subject><subject>Electrocatalysis</subject><subject>Electrocatalysts</subject><subject>electrochemistry</subject><subject>Energy efficiency</subject><subject>Epitaxial growth</subject><subject>Ethylene glycol</subject><subject>Fuel cells</subject><subject>mesoporous metals</subject><subject>nanoparticles</subject><subject>Nitrate reduction</subject><subject>Nucleation</subject><subject>Oxidation</subject><subject>Phase separation</subject><subject>Reduction</subject><subject>Selectivity</subject><subject>single crystals</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkT9v1DAYhy0Eou3ByogssbDk8J-L47CVEMpJpUUqzJYvftNz5bMPOylk68iIGPl4_ST4dKVILEyvX_vx89r6IfSMkjklhL3S3sKcEbbIjaQP0CEtGS14VfGHeb3gvKhkSQ_QUUpXO0QS8RgdcMl5LSk9RL-W8fbmx9uwBYOb8aPBF9ZfOsh7TZzSoJ2zHvAHSGEbYhgTPtM-DDBEvQYTg0-4DxG3w3pykMETN3XB4fNv1ujBBo9bB90QQ6ezako2vcatX2vf5XEXsDuz14AbB_paXwIOPW5uv_9s8JvgzRP0qNcuwdO7OkOf37WfmvfF6fnJsjk-LTpecVoA60Sp9aomRHSlMJJxIWltGOO8rOoKepO7mnNRC1KLVUZyYdIw0-u-LPkMvdx7tzF8GSENamNTB85pD_nHitWszO5KLjL64h_0KozR59cpThgVXLI8dobme6qLIaUIvdpGu9FxUpSoXWpql5q6Ty1feH6nHVcbMPf4n5gyUO-Br9bB9B-dOj5btn_lvwHkN6ct</recordid><startdate>20240408</startdate><enddate>20240408</enddate><creator>Lv, Hao</creator><creator>Mao, Yumeng</creator><creator>Yao, Huiqin</creator><creator>Ma, Huazhong</creator><creator>Han, Chenyu</creator><creator>Yang, Yao‐Yue</creator><creator>Qiao, Zhen‐An</creator><creator>Liu, Ben</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6064-9360</orcidid></search><sort><creationdate>20240408</creationdate><title>Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond</title><author>Lv, Hao ; Mao, Yumeng ; Yao, Huiqin ; Ma, Huazhong ; Han, Chenyu ; Yang, Yao‐Yue ; Qiao, Zhen‐An ; Liu, Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3731-e2c65aab9006c56d8236819d22335797efd19d933696096b56d09628d2dfaf553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Catalysis</topic><topic>Chemical composition</topic><topic>Chemical synthesis</topic><topic>Cleavage</topic><topic>C−C bond cleavage</topic><topic>Electrocatalysis</topic><topic>Electrocatalysts</topic><topic>electrochemistry</topic><topic>Energy efficiency</topic><topic>Epitaxial growth</topic><topic>Ethylene glycol</topic><topic>Fuel cells</topic><topic>mesoporous metals</topic><topic>nanoparticles</topic><topic>Nitrate reduction</topic><topic>Nucleation</topic><topic>Oxidation</topic><topic>Phase separation</topic><topic>Reduction</topic><topic>Selectivity</topic><topic>single crystals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lv, Hao</creatorcontrib><creatorcontrib>Mao, Yumeng</creatorcontrib><creatorcontrib>Yao, Huiqin</creatorcontrib><creatorcontrib>Ma, Huazhong</creatorcontrib><creatorcontrib>Han, Chenyu</creatorcontrib><creatorcontrib>Yang, Yao‐Yue</creatorcontrib><creatorcontrib>Qiao, Zhen‐An</creatorcontrib><creatorcontrib>Liu, Ben</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lv, Hao</au><au>Mao, Yumeng</au><au>Yao, Huiqin</au><au>Ma, Huazhong</au><au>Han, Chenyu</au><au>Yang, Yao‐Yue</au><au>Qiao, Zhen‐An</au><au>Liu, Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2024-04-08</date><risdate>2024</risdate><volume>63</volume><issue>15</issue><spage>e202400281</spage><epage>n/a</epage><pages>e202400281-n/a</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>The development of highly efficient electrocatalysts for complete oxidation of ethylene glycol (EG) in direct EG fuel cells is of decisive importance to hold higher energy efficiency. Despite some achievements, their progress, especially electrocatalytic selectivity to complete oxidated C1 products, is remarkably slower than expected. In this work, we developed a facile aqueous synthesis of Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) as high‐performance electrocatalyst for promoting oxidation cleavage of C−C bond in alkaline EG oxidation reaction (EGOR) electrocatalysis. The synthesis relied on precise reduction/co‐nucleation and epitaxial growth of Ir, Cu and Pd precursors with cetyltrimethylammonium chloride as the mesopore‐forming surfactant and extra Br− as the facet‐selective agent under ambient conditions. The products featured concave nanotetrahedron morphology enclosed by well‐defined (111) facets, single‐crystalline and mesoporous structure radiated from the center, and uniform elemental composition without any phase separation. Ir‐CuPd SMTs disclosed remarkably enhanced electrocatalytic activity and excellent stability as well as superior selectivity of C1 products for alkaline EGOR electrocatalysis. Detailed mechanism studies demonstrated that performance improvement came from structural and compositional synergies, which kinetically accelerated transports of electrons/reactants within active sites of penetrated mesopores and facilitated oxidation cleavage of high‐energy‐barrier C−C bond of EG for desired C1 products. More interestingly, Ir‐CuPd SMTs performed well in coupled electrocatalysis of anode EGOR and cathode nitrate reduction, highlighting its high potential as bifunctional electrocatalyst in various applications. Ir‐doped CuPd single‐crystalline mesoporous nanotetrahedrons (Ir‐CuPd SMTs) were facilely prepared through an aqueous surfactant‐templating epitaxial growth strategy. With mesoporous channels and multi‐compositions, Ir‐CuPd SMTs delivered remarkable C−C bond cleavage of electrocatalytic ethylene glycol oxidation (EGOR) to C1 products. The Ir‐CuPd SMTs performed perfectly in coupled electrocatalysis of EGOR and nitrate reduction.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38339811</pmid><doi>10.1002/anie.202400281</doi><tpages>10</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-6064-9360</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2024-04, Vol.63 (15), p.e202400281-n/a
issn 1433-7851
1521-3773
language eng
recordid cdi_proquest_miscellaneous_2925006784
source Wiley Journals
subjects Catalysis
Chemical composition
Chemical synthesis
Cleavage
C−C bond cleavage
Electrocatalysis
Electrocatalysts
electrochemistry
Energy efficiency
Epitaxial growth
Ethylene glycol
Fuel cells
mesoporous metals
nanoparticles
Nitrate reduction
Nucleation
Oxidation
Phase separation
Reduction
Selectivity
single crystals
title Ir‐Doped CuPd Single‐Crystalline Mesoporous Nanotetrahedrons for Ethylene Glycol Oxidation Electrocatalysis: Enhanced Selective Cleavage of C−C Bond
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T12%3A02%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ir%E2%80%90Doped%20CuPd%20Single%E2%80%90Crystalline%20Mesoporous%20Nanotetrahedrons%20for%20Ethylene%20Glycol%20Oxidation%20Electrocatalysis:%20Enhanced%20Selective%20Cleavage%20of%20C%E2%88%92C%20Bond&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Lv,%20Hao&rft.date=2024-04-08&rft.volume=63&rft.issue=15&rft.spage=e202400281&rft.epage=n/a&rft.pages=e202400281-n/a&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202400281&rft_dat=%3Cproquest_cross%3E2925006784%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3021638222&rft_id=info:pmid/38339811&rfr_iscdi=true