Controllable interfacial electron transfer induced by heterointerfaced sulfur-based catalysts with less electronegative anions for boosted hydrogen evolution reaction in the universal pH range
Economic cobalt-sulfide (Co x S y )-based electrocatalysts play a vital role in the hydrogen evolution reaction (HER) due to their adjustable electronic structure and environmental friendliness. However, the limited active sites, poor structural stability and intense hydrogen (H) adsorption energy o...
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creator | Chu, Dawei Wei, Xiaoling Song, Xiumei Zhang, Zhen Tan, Lichao Ma, Huiyuan Pang, Haijun Wang, Xin Chen, Zhongwei |
description | Economic cobalt-sulfide (Co
x
S
y
)-based electrocatalysts play a vital role in the hydrogen evolution reaction (HER) due to their adjustable electronic structure and environmental friendliness. However, the limited active sites, poor structural stability and intense hydrogen (H) adsorption energy of these catalysts endow them with unsatisfactory performance, which significantly impedes their practical application in acidic/alkaline/neutral media. Herein, we designed a series of defective nickel-cobalt sulfur-based catalysts with an enriched heterogeneous interface. The P anions not only offer ample sulfur defects for charge movement, but also provide a protection layer to prevent structural collapse in acidic/alkaline media. More importantly, the P element with low electronegativity slightly lowers the robust strength of S-H bonds, yet maintains the activity of the S-based catalysts, thereby balancing the adsorption/release of H. Subsequently, the introduction of the heterointerface accompanied by P creates controllable interfacial electron transfer between Ni-based components (Ni
3
S
x
P
y
) and Co components (Co
3
S
x
P
y
), which can regulate the charge state and enhance charge transfer kinetics for boosted HER. Meanwhile, the planar structure establishes a highly conductive network for facilitated ion/electron transportation, leading to an accelerated redox reaction. Attributed to its structural benefits, an admirable HER performance with an optimum overpotential of 56 mV and a Tafel slope of 74 mV dec
−1
with −10 mA cm
−2
in 1 M KOH and decent long-term stability can be achieved. This work paves the way for S-based catalyst design to achieve superior HER performance in the universal pH range.
Defective cross linked nickel cobalt sulfide sheets dominated by phosphorus anions and a hetero interface were designed. The catalyst possesses surprising HER properties with low overpotentials and long term stability. |
doi_str_mv | 10.1039/d2ta06240b |
format | Article |
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x
S
y
)-based electrocatalysts play a vital role in the hydrogen evolution reaction (HER) due to their adjustable electronic structure and environmental friendliness. However, the limited active sites, poor structural stability and intense hydrogen (H) adsorption energy of these catalysts endow them with unsatisfactory performance, which significantly impedes their practical application in acidic/alkaline/neutral media. Herein, we designed a series of defective nickel-cobalt sulfur-based catalysts with an enriched heterogeneous interface. The P anions not only offer ample sulfur defects for charge movement, but also provide a protection layer to prevent structural collapse in acidic/alkaline media. More importantly, the P element with low electronegativity slightly lowers the robust strength of S-H bonds, yet maintains the activity of the S-based catalysts, thereby balancing the adsorption/release of H. Subsequently, the introduction of the heterointerface accompanied by P creates controllable interfacial electron transfer between Ni-based components (Ni
3
S
x
P
y
) and Co components (Co
3
S
x
P
y
), which can regulate the charge state and enhance charge transfer kinetics for boosted HER. Meanwhile, the planar structure establishes a highly conductive network for facilitated ion/electron transportation, leading to an accelerated redox reaction. Attributed to its structural benefits, an admirable HER performance with an optimum overpotential of 56 mV and a Tafel slope of 74 mV dec
−1
with −10 mA cm
−2
in 1 M KOH and decent long-term stability can be achieved. This work paves the way for S-based catalyst design to achieve superior HER performance in the universal pH range.
Defective cross linked nickel cobalt sulfide sheets dominated by phosphorus anions and a hetero interface were designed. The catalyst possesses surprising HER properties with low overpotentials and long term stability.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/d2ta06240b</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Adsorption ; Anions ; Bonding strength ; Catalysts ; Charge transfer ; Cobalt ; Cobalt sulfide ; Electrocatalysts ; Electron transfer ; Electronegativity ; Electronic structure ; Hydrogen ; Hydrogen evolution reactions ; Nickel ; pH effects ; Planar structures ; Redox reactions ; Structural stability ; Sulfur</subject><ispartof>Journal of materials chemistry. A, Materials for energy and sustainability, 2022-10, Vol.1 (4), p.21683-21689</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-45f9d24539bcdfbda1e5a4e398a8246ea7c0a41786378caa9b5b24cde98125503</citedby><cites>FETCH-LOGICAL-c281t-45f9d24539bcdfbda1e5a4e398a8246ea7c0a41786378caa9b5b24cde98125503</cites><orcidid>0000-0002-0405-8352 ; 0000-0003-3463-5509</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Chu, Dawei</creatorcontrib><creatorcontrib>Wei, Xiaoling</creatorcontrib><creatorcontrib>Song, Xiumei</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Tan, Lichao</creatorcontrib><creatorcontrib>Ma, Huiyuan</creatorcontrib><creatorcontrib>Pang, Haijun</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Chen, Zhongwei</creatorcontrib><title>Controllable interfacial electron transfer induced by heterointerfaced sulfur-based catalysts with less electronegative anions for boosted hydrogen evolution reaction in the universal pH range</title><title>Journal of materials chemistry. A, Materials for energy and sustainability</title><description>Economic cobalt-sulfide (Co
x
S
y
)-based electrocatalysts play a vital role in the hydrogen evolution reaction (HER) due to their adjustable electronic structure and environmental friendliness. However, the limited active sites, poor structural stability and intense hydrogen (H) adsorption energy of these catalysts endow them with unsatisfactory performance, which significantly impedes their practical application in acidic/alkaline/neutral media. Herein, we designed a series of defective nickel-cobalt sulfur-based catalysts with an enriched heterogeneous interface. The P anions not only offer ample sulfur defects for charge movement, but also provide a protection layer to prevent structural collapse in acidic/alkaline media. More importantly, the P element with low electronegativity slightly lowers the robust strength of S-H bonds, yet maintains the activity of the S-based catalysts, thereby balancing the adsorption/release of H. Subsequently, the introduction of the heterointerface accompanied by P creates controllable interfacial electron transfer between Ni-based components (Ni
3
S
x
P
y
) and Co components (Co
3
S
x
P
y
), which can regulate the charge state and enhance charge transfer kinetics for boosted HER. Meanwhile, the planar structure establishes a highly conductive network for facilitated ion/electron transportation, leading to an accelerated redox reaction. Attributed to its structural benefits, an admirable HER performance with an optimum overpotential of 56 mV and a Tafel slope of 74 mV dec
−1
with −10 mA cm
−2
in 1 M KOH and decent long-term stability can be achieved. This work paves the way for S-based catalyst design to achieve superior HER performance in the universal pH range.
Defective cross linked nickel cobalt sulfide sheets dominated by phosphorus anions and a hetero interface were designed. The catalyst possesses surprising HER properties with low overpotentials and long term stability.</description><subject>Adsorption</subject><subject>Anions</subject><subject>Bonding strength</subject><subject>Catalysts</subject><subject>Charge transfer</subject><subject>Cobalt</subject><subject>Cobalt sulfide</subject><subject>Electrocatalysts</subject><subject>Electron transfer</subject><subject>Electronegativity</subject><subject>Electronic structure</subject><subject>Hydrogen</subject><subject>Hydrogen evolution reactions</subject><subject>Nickel</subject><subject>pH effects</subject><subject>Planar structures</subject><subject>Redox reactions</subject><subject>Structural stability</subject><subject>Sulfur</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpFkUFr3DAQhU1JoGGbS-4FQW4Bt7Js2dJxu0m6hUAvydmM5PGugyptNPKG_Xf9aVWy7VYHaaT3zejBK4qrin-peK2_DiIBb0XDzYfiQnDJy67R7dmpVupjcUn0zPNSnLdaXxS_V8GnGJwD45BNPmEcwU7gGDq0WfEsRfA0YszqMFscmDmwLWYw_MPzG81unGNpgPLFQgJ3oETsdUpb5pDoNA43kKY9MvBT8MTGEJkJgVJu2x6GGDboGe6Dm1PWWUSw78WUfWyRzT73Rsr2dmuWfW3wU3E-giO8_Hsuiqf7u8fVunz4-f3HavlQWqGqVDZy1INoZK2NHUYzQIUSGqy1AiWaFqGzHJqqU23dKQugjTSisQNqVQkpeb0oro9zdzG8zEipfw5z9PnLXnRCqrzVMlM3R8rGQBRx7Hdx-gXx0Fe8fwupvxWPy_eQvmX48xGOZE_c_xDrP0gclKI</recordid><startdate>20221018</startdate><enddate>20221018</enddate><creator>Chu, Dawei</creator><creator>Wei, Xiaoling</creator><creator>Song, Xiumei</creator><creator>Zhang, Zhen</creator><creator>Tan, Lichao</creator><creator>Ma, Huiyuan</creator><creator>Pang, Haijun</creator><creator>Wang, Xin</creator><creator>Chen, Zhongwei</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><scope>L7M</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-0405-8352</orcidid><orcidid>https://orcid.org/0000-0003-3463-5509</orcidid></search><sort><creationdate>20221018</creationdate><title>Controllable interfacial electron transfer induced by heterointerfaced sulfur-based catalysts with less electronegative anions for boosted hydrogen evolution reaction in the universal pH range</title><author>Chu, Dawei ; Wei, Xiaoling ; Song, Xiumei ; Zhang, Zhen ; Tan, Lichao ; Ma, Huiyuan ; Pang, Haijun ; Wang, Xin ; Chen, Zhongwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-45f9d24539bcdfbda1e5a4e398a8246ea7c0a41786378caa9b5b24cde98125503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adsorption</topic><topic>Anions</topic><topic>Bonding strength</topic><topic>Catalysts</topic><topic>Charge transfer</topic><topic>Cobalt</topic><topic>Cobalt sulfide</topic><topic>Electrocatalysts</topic><topic>Electron transfer</topic><topic>Electronegativity</topic><topic>Electronic structure</topic><topic>Hydrogen</topic><topic>Hydrogen evolution reactions</topic><topic>Nickel</topic><topic>pH effects</topic><topic>Planar structures</topic><topic>Redox reactions</topic><topic>Structural stability</topic><topic>Sulfur</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chu, Dawei</creatorcontrib><creatorcontrib>Wei, Xiaoling</creatorcontrib><creatorcontrib>Song, Xiumei</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Tan, Lichao</creatorcontrib><creatorcontrib>Ma, Huiyuan</creatorcontrib><creatorcontrib>Pang, Haijun</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Chen, Zhongwei</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chu, Dawei</au><au>Wei, Xiaoling</au><au>Song, Xiumei</au><au>Zhang, Zhen</au><au>Tan, Lichao</au><au>Ma, Huiyuan</au><au>Pang, Haijun</au><au>Wang, Xin</au><au>Chen, Zhongwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controllable interfacial electron transfer induced by heterointerfaced sulfur-based catalysts with less electronegative anions for boosted hydrogen evolution reaction in the universal pH range</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2022-10-18</date><risdate>2022</risdate><volume>1</volume><issue>4</issue><spage>21683</spage><epage>21689</epage><pages>21683-21689</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>Economic cobalt-sulfide (Co
x
S
y
)-based electrocatalysts play a vital role in the hydrogen evolution reaction (HER) due to their adjustable electronic structure and environmental friendliness. However, the limited active sites, poor structural stability and intense hydrogen (H) adsorption energy of these catalysts endow them with unsatisfactory performance, which significantly impedes their practical application in acidic/alkaline/neutral media. Herein, we designed a series of defective nickel-cobalt sulfur-based catalysts with an enriched heterogeneous interface. The P anions not only offer ample sulfur defects for charge movement, but also provide a protection layer to prevent structural collapse in acidic/alkaline media. More importantly, the P element with low electronegativity slightly lowers the robust strength of S-H bonds, yet maintains the activity of the S-based catalysts, thereby balancing the adsorption/release of H. Subsequently, the introduction of the heterointerface accompanied by P creates controllable interfacial electron transfer between Ni-based components (Ni
3
S
x
P
y
) and Co components (Co
3
S
x
P
y
), which can regulate the charge state and enhance charge transfer kinetics for boosted HER. Meanwhile, the planar structure establishes a highly conductive network for facilitated ion/electron transportation, leading to an accelerated redox reaction. Attributed to its structural benefits, an admirable HER performance with an optimum overpotential of 56 mV and a Tafel slope of 74 mV dec
−1
with −10 mA cm
−2
in 1 M KOH and decent long-term stability can be achieved. This work paves the way for S-based catalyst design to achieve superior HER performance in the universal pH range.
Defective cross linked nickel cobalt sulfide sheets dominated by phosphorus anions and a hetero interface were designed. The catalyst possesses surprising HER properties with low overpotentials and long term stability.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2ta06240b</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0405-8352</orcidid><orcidid>https://orcid.org/0000-0003-3463-5509</orcidid></addata></record> |
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identifier | ISSN: 2050-7488 |
ispartof | Journal of materials chemistry. A, Materials for energy and sustainability, 2022-10, Vol.1 (4), p.21683-21689 |
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language | eng |
recordid | cdi_rsc_primary_d2ta06240b |
source | Royal Society Of Chemistry Journals 2008- |
subjects | Adsorption Anions Bonding strength Catalysts Charge transfer Cobalt Cobalt sulfide Electrocatalysts Electron transfer Electronegativity Electronic structure Hydrogen Hydrogen evolution reactions Nickel pH effects Planar structures Redox reactions Structural stability Sulfur |
title | Controllable interfacial electron transfer induced by heterointerfaced sulfur-based catalysts with less electronegative anions for boosted hydrogen evolution reaction in the universal pH range |
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