Sulfur-bridge ligands altering the microenvironment of single-atom CoNS sites to boost the oxygen reduction reaction
We report here an asymmetric N,S-coordinated cobalt-based single-atom catalyst with sulfur (S)-bridge ligands (Co-N/S-C) for the oxygen reduction reaction (ORR). The Co-N/S-C exhibits a half-wave potential ( E 1/2 ) of 0.908 V versus RHE, outperforming most state-of-the-art ORR catalysts. Theoretica...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-04, Vol.6 (3), p.464-467 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Liu, Feng Guo, Yingchun Zhong, Yan Li, Jingsha Zhang, Heng Shi, Lei Lin, Xuanni Ye, Fenghui Ge, Kai Yuan, Shuai Hu, Chuangang Guo, Chunxian |
description | We report here an asymmetric N,S-coordinated cobalt-based single-atom catalyst with sulfur (S)-bridge ligands (Co-N/S-C) for the oxygen reduction reaction (ORR). The Co-N/S-C exhibits a half-wave potential (
E
1/2
) of 0.908 V
versus
RHE, outperforming most state-of-the-art ORR catalysts. Theoretical calculations indicate that the CoN
3
SC
10
-S moiety facilitates the ORR kinetics by optimizing the adsorption of intermediates. This work provides new insights into the design of single-atom catalysts for electrocatalysis through heteroatom-bridge ligand engineering.
The unique S-bridge ligands' synergistic CoN
3
S sites in Co-N/S-C have optimal adsorption-desorption and lower energy barriers of ORR intermediates, thus boosting the ORR activity. |
doi_str_mv | 10.1039/d4cc00854e |
format | Article |
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E
1/2
) of 0.908 V
versus
RHE, outperforming most state-of-the-art ORR catalysts. Theoretical calculations indicate that the CoN
3
SC
10
-S moiety facilitates the ORR kinetics by optimizing the adsorption of intermediates. This work provides new insights into the design of single-atom catalysts for electrocatalysis through heteroatom-bridge ligand engineering.
The unique S-bridge ligands' synergistic CoN
3
S sites in Co-N/S-C have optimal adsorption-desorption and lower energy barriers of ORR intermediates, thus boosting the ORR activity.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d4cc00854e</identifier><ispartof>Chemical communications (Cambridge, England), 2024-04, Vol.6 (3), p.464-467</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>315,781,785,27928,27929</link.rule.ids></links><search><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Guo, Yingchun</creatorcontrib><creatorcontrib>Zhong, Yan</creatorcontrib><creatorcontrib>Li, Jingsha</creatorcontrib><creatorcontrib>Zhang, Heng</creatorcontrib><creatorcontrib>Shi, Lei</creatorcontrib><creatorcontrib>Lin, Xuanni</creatorcontrib><creatorcontrib>Ye, Fenghui</creatorcontrib><creatorcontrib>Ge, Kai</creatorcontrib><creatorcontrib>Yuan, Shuai</creatorcontrib><creatorcontrib>Hu, Chuangang</creatorcontrib><creatorcontrib>Guo, Chunxian</creatorcontrib><title>Sulfur-bridge ligands altering the microenvironment of single-atom CoNS sites to boost the oxygen reduction reaction</title><title>Chemical communications (Cambridge, England)</title><description>We report here an asymmetric N,S-coordinated cobalt-based single-atom catalyst with sulfur (S)-bridge ligands (Co-N/S-C) for the oxygen reduction reaction (ORR). The Co-N/S-C exhibits a half-wave potential (
E
1/2
) of 0.908 V
versus
RHE, outperforming most state-of-the-art ORR catalysts. Theoretical calculations indicate that the CoN
3
SC
10
-S moiety facilitates the ORR kinetics by optimizing the adsorption of intermediates. This work provides new insights into the design of single-atom catalysts for electrocatalysis through heteroatom-bridge ligand engineering.
The unique S-bridge ligands' synergistic CoN
3
S sites in Co-N/S-C have optimal adsorption-desorption and lower energy barriers of ORR intermediates, thus boosting the ORR activity.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj71OAzEQhK0IJMJPQ4-0L2Dw6ezkUkcgKpqkoIsc395h5PNG6z1E3p5LhETJNPNpRlOMUveVeaxMvXpqbQjGNM7iTM2remG1s837xYndSi9r667UdSmfZlLlmrmSzZi6kfWeY9sjpNj73BbwSZBj7kE-EIYYmDB_RaY8YBagDspUJtReaIA1vW2mQLCAEOyJipx39H3sMQNjOwaJdCJ_hlt12flU8O7Xb9TDy_N2_aq5hN2B4-D5uPu7Uv_X_wB6xU8Q</recordid><startdate>20240409</startdate><enddate>20240409</enddate><creator>Liu, Feng</creator><creator>Guo, Yingchun</creator><creator>Zhong, Yan</creator><creator>Li, Jingsha</creator><creator>Zhang, Heng</creator><creator>Shi, Lei</creator><creator>Lin, Xuanni</creator><creator>Ye, Fenghui</creator><creator>Ge, Kai</creator><creator>Yuan, Shuai</creator><creator>Hu, Chuangang</creator><creator>Guo, Chunxian</creator><scope/></search><sort><creationdate>20240409</creationdate><title>Sulfur-bridge ligands altering the microenvironment of single-atom CoNS sites to boost the oxygen reduction reaction</title><author>Liu, Feng ; Guo, Yingchun ; Zhong, Yan ; Li, Jingsha ; Zhang, Heng ; Shi, Lei ; Lin, Xuanni ; Ye, Fenghui ; Ge, Kai ; Yuan, Shuai ; Hu, Chuangang ; Guo, Chunxian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d4cc00854e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Feng</creatorcontrib><creatorcontrib>Guo, Yingchun</creatorcontrib><creatorcontrib>Zhong, Yan</creatorcontrib><creatorcontrib>Li, Jingsha</creatorcontrib><creatorcontrib>Zhang, Heng</creatorcontrib><creatorcontrib>Shi, Lei</creatorcontrib><creatorcontrib>Lin, Xuanni</creatorcontrib><creatorcontrib>Ye, Fenghui</creatorcontrib><creatorcontrib>Ge, Kai</creatorcontrib><creatorcontrib>Yuan, Shuai</creatorcontrib><creatorcontrib>Hu, Chuangang</creatorcontrib><creatorcontrib>Guo, Chunxian</creatorcontrib><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Feng</au><au>Guo, Yingchun</au><au>Zhong, Yan</au><au>Li, Jingsha</au><au>Zhang, Heng</au><au>Shi, Lei</au><au>Lin, Xuanni</au><au>Ye, Fenghui</au><au>Ge, Kai</au><au>Yuan, Shuai</au><au>Hu, Chuangang</au><au>Guo, Chunxian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sulfur-bridge ligands altering the microenvironment of single-atom CoNS sites to boost the oxygen reduction reaction</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2024-04-09</date><risdate>2024</risdate><volume>6</volume><issue>3</issue><spage>464</spage><epage>467</epage><pages>464-467</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>We report here an asymmetric N,S-coordinated cobalt-based single-atom catalyst with sulfur (S)-bridge ligands (Co-N/S-C) for the oxygen reduction reaction (ORR). The Co-N/S-C exhibits a half-wave potential (
E
1/2
) of 0.908 V
versus
RHE, outperforming most state-of-the-art ORR catalysts. Theoretical calculations indicate that the CoN
3
SC
10
-S moiety facilitates the ORR kinetics by optimizing the adsorption of intermediates. This work provides new insights into the design of single-atom catalysts for electrocatalysis through heteroatom-bridge ligand engineering.
The unique S-bridge ligands' synergistic CoN
3
S sites in Co-N/S-C have optimal adsorption-desorption and lower energy barriers of ORR intermediates, thus boosting the ORR activity.</abstract><doi>10.1039/d4cc00854e</doi><tpages>4</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
title | Sulfur-bridge ligands altering the microenvironment of single-atom CoNS sites to boost the oxygen reduction reaction |
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