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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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-10, Vol.1 (4), p.21683-21689
Hauptverfasser: Chu, Dawei, Wei, Xiaoling, Song, Xiumei, Zhang, Zhen, Tan, Lichao, Ma, Huiyuan, Pang, Haijun, Wang, Xin, Chen, Zhongwei
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container_issue 4
container_start_page 21683
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 1
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.
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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. 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Defective cross linked nickel cobalt sulfide sheets dominated by phosphorus anions and a hetero interface were designed. 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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. 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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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