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Construction of a highly efficient MoS-based composite electrocatalyst for the oxygen evolution reaction
Molybdenum disulfide (MoS 2 ) has great potential for the catalysis of the oxygen evolution reaction (OER) due to its suitable valence band edge. However, the high adsorption energy barriers of the key intermediates *OH and *OOH at the catalytic sites severely limit its catalytic activity. In this r...
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Published in: | Catalysis science & technology 2024-10, Vol.14 (21), p.638-6392 |
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container_title | Catalysis science & technology |
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creator | Huang, Mengyan Liu, Bo Wu, Junwei Gu, Junfeng Zheng, Yichen Ma, Peiyan Li, Bei Fu, Zhengyi |
description | Molybdenum disulfide (MoS
2
) has great potential for the catalysis of the oxygen evolution reaction (OER) due to its suitable valence band edge. However, the high adsorption energy barriers of the key intermediates *OH and *OOH at the catalytic sites severely limit its catalytic activity. In this research, we designed a carboxyl-decorated MoC@MoS
2
composite (CC-MoC@MoS
2
) electrocatalyst for OER, in which the S sites of MoS
2
provide effective adsorption of the two intermediates. The optimized CC-MoC@MoS
2
could catalyze OER rapidly and stably, reaching current densities of 10, 50 and 100 mA cm
−2
in alkaline medium at overpotentials of 248, 307 and 359 mV, respectively.
The carboxyl groups in CC-MoC@MoS
2
play a similar role to the amino acid residues in PS II. |
doi_str_mv | 10.1039/d4cy00923a |
format | article |
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2
) has great potential for the catalysis of the oxygen evolution reaction (OER) due to its suitable valence band edge. However, the high adsorption energy barriers of the key intermediates *OH and *OOH at the catalytic sites severely limit its catalytic activity. In this research, we designed a carboxyl-decorated MoC@MoS
2
composite (CC-MoC@MoS
2
) electrocatalyst for OER, in which the S sites of MoS
2
provide effective adsorption of the two intermediates. The optimized CC-MoC@MoS
2
could catalyze OER rapidly and stably, reaching current densities of 10, 50 and 100 mA cm
−2
in alkaline medium at overpotentials of 248, 307 and 359 mV, respectively.
The carboxyl groups in CC-MoC@MoS
2
play a similar role to the amino acid residues in PS II.</description><identifier>ISSN: 2044-4753</identifier><identifier>EISSN: 2044-4761</identifier><identifier>DOI: 10.1039/d4cy00923a</identifier><ispartof>Catalysis science & technology, 2024-10, Vol.14 (21), p.638-6392</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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Huang, Mengyan</creatorcontrib><creatorcontrib>Liu, Bo</creatorcontrib><creatorcontrib>Wu, Junwei</creatorcontrib><creatorcontrib>Gu, Junfeng</creatorcontrib><creatorcontrib>Zheng, Yichen</creatorcontrib><creatorcontrib>Ma, Peiyan</creatorcontrib><creatorcontrib>Li, Bei</creatorcontrib><creatorcontrib>Fu, Zhengyi</creatorcontrib><title>Construction of a highly efficient MoS-based composite electrocatalyst for the oxygen evolution reaction</title><title>Catalysis science & technology</title><description>Molybdenum disulfide (MoS
2
) has great potential for the catalysis of the oxygen evolution reaction (OER) due to its suitable valence band edge. However, the high adsorption energy barriers of the key intermediates *OH and *OOH at the catalytic sites severely limit its catalytic activity. In this research, we designed a carboxyl-decorated MoC@MoS
2
composite (CC-MoC@MoS
2
) electrocatalyst for OER, in which the S sites of MoS
2
provide effective adsorption of the two intermediates. The optimized CC-MoC@MoS
2
could catalyze OER rapidly and stably, reaching current densities of 10, 50 and 100 mA cm
−2
in alkaline medium at overpotentials of 248, 307 and 359 mV, respectively.
The carboxyl groups in CC-MoC@MoS
2
play a similar role to the amino acid residues in PS II.</description><issn>2044-4753</issn><issn>2044-4761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFjz0LwjAURYMoKNrFXXh_oJq28aOzKC5OukuML20k9kkSxfx7RURH73IvHDhwGRtmfJzxopychIqcl3khW6yXcyFSMZ9l7e-eFl2WeH_mr4gy44u8x-olNT64mwqGGiANEmpT1TYCam2UwSbAlnbpUXo8gaLLlbwJCGhRBUdKBmmjD6DJQagR6BErbADvZG9vpUP5dg9YR0vrMfl0n43Wq_1ykzqvDldnLtLFw-9B8Y8_ARw0S3E</recordid><startdate>20241028</startdate><enddate>20241028</enddate><creator>Huang, Mengyan</creator><creator>Liu, Bo</creator><creator>Wu, Junwei</creator><creator>Gu, Junfeng</creator><creator>Zheng, Yichen</creator><creator>Ma, Peiyan</creator><creator>Li, Bei</creator><creator>Fu, Zhengyi</creator><scope/></search><sort><creationdate>20241028</creationdate><title>Construction of a highly efficient MoS-based composite electrocatalyst for the oxygen evolution reaction</title><author>Huang, Mengyan ; Liu, Bo ; Wu, Junwei ; Gu, Junfeng ; Zheng, Yichen ; Ma, Peiyan ; Li, Bei ; Fu, Zhengyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d4cy00923a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Mengyan</creatorcontrib><creatorcontrib>Liu, Bo</creatorcontrib><creatorcontrib>Wu, Junwei</creatorcontrib><creatorcontrib>Gu, Junfeng</creatorcontrib><creatorcontrib>Zheng, Yichen</creatorcontrib><creatorcontrib>Ma, Peiyan</creatorcontrib><creatorcontrib>Li, Bei</creatorcontrib><creatorcontrib>Fu, Zhengyi</creatorcontrib><jtitle>Catalysis science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Mengyan</au><au>Liu, Bo</au><au>Wu, Junwei</au><au>Gu, Junfeng</au><au>Zheng, Yichen</au><au>Ma, Peiyan</au><au>Li, Bei</au><au>Fu, Zhengyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of a highly efficient MoS-based composite electrocatalyst for the oxygen evolution reaction</atitle><jtitle>Catalysis science & technology</jtitle><date>2024-10-28</date><risdate>2024</risdate><volume>14</volume><issue>21</issue><spage>638</spage><epage>6392</epage><pages>638-6392</pages><issn>2044-4753</issn><eissn>2044-4761</eissn><abstract>Molybdenum disulfide (MoS
2
) has great potential for the catalysis of the oxygen evolution reaction (OER) due to its suitable valence band edge. However, the high adsorption energy barriers of the key intermediates *OH and *OOH at the catalytic sites severely limit its catalytic activity. In this research, we designed a carboxyl-decorated MoC@MoS
2
composite (CC-MoC@MoS
2
) electrocatalyst for OER, in which the S sites of MoS
2
provide effective adsorption of the two intermediates. The optimized CC-MoC@MoS
2
could catalyze OER rapidly and stably, reaching current densities of 10, 50 and 100 mA cm
−2
in alkaline medium at overpotentials of 248, 307 and 359 mV, respectively.
The carboxyl groups in CC-MoC@MoS
2
play a similar role to the amino acid residues in PS II.</abstract><doi>10.1039/d4cy00923a</doi><tpages>13</tpages></addata></record> |
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source | Royal Society of Chemistry |
title | Construction of a highly efficient MoS-based composite electrocatalyst for the oxygen evolution reaction |
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