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- Publisher Website: 10.1002/anie.201602237
- Scopus: eid_2-s2.0-84992297638
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Article: Interface Engineering of MoS2 /Ni3 S2 Heterostructures for Highly Enhanced Electrochemical Overall-Water-Splitting Activity
Title | Interface Engineering of MoS<inf>2</inf>/Ni<inf>3</inf>S<inf>2</inf>Heterostructures for Highly Enhanced Electrochemical Overall-Water-Splitting Activity |
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Authors | |
Keywords | electrocatalysts interface engineering molybdenum disulfide nickel sulfide water splitting |
Issue Date | 2016 |
Citation | Angewandte Chemie - International Edition, 2016, v. 55, n. 23, p. 6702-6707 How to Cite? |
Abstract | To achieve sustainable production of H2fuel through water splitting, low-cost electrocatalysts for the hydrogen-evolution reaction (HER) and the oxygen-evolution reaction (OER) are required to replace Pt and IrO2catalysts. Herein, for the first time, we present the interface engineering of novel MoS2/Ni3S2heterostructures, in which abundant interfaces are formed. For OER, such MoS2/Ni3S2heterostructures show an extremely low overpotential of ca. 218 mV at 10 mA cm-2, which is superior to that of the state-of-the-art OER electrocatalysts. Using MoS2/Ni3S2heterostructures as bifunctional electrocatalysts, an alkali electrolyzer delivers a current density of 10 mA cm-2at a very low cell voltage of ca. 1.56 V. In combination with DFT calculations, this study demonstrates that the constructed interfaces synergistically favor the chemisorption of hydrogen and oxygen-containing intermediates, thus accelerating the overall electrochemical water splitting. |
Persistent Identifier | http://hdl.handle.net/10722/348889 |
ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 |
DC Field | Value | Language |
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dc.contributor.author | Zhang, Jian | - |
dc.contributor.author | Wang, Tao | - |
dc.contributor.author | Pohl, Darius | - |
dc.contributor.author | Rellinghaus, Bernd | - |
dc.contributor.author | Dong, Renhao | - |
dc.contributor.author | Liu, Shaohua | - |
dc.contributor.author | Zhuang, Xiaodong | - |
dc.contributor.author | Feng, Xinliang | - |
dc.date.accessioned | 2024-10-17T06:54:45Z | - |
dc.date.available | 2024-10-17T06:54:45Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Angewandte Chemie - International Edition, 2016, v. 55, n. 23, p. 6702-6707 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.uri | http://hdl.handle.net/10722/348889 | - |
dc.description.abstract | To achieve sustainable production of H2fuel through water splitting, low-cost electrocatalysts for the hydrogen-evolution reaction (HER) and the oxygen-evolution reaction (OER) are required to replace Pt and IrO2catalysts. Herein, for the first time, we present the interface engineering of novel MoS2/Ni3S2heterostructures, in which abundant interfaces are formed. For OER, such MoS2/Ni3S2heterostructures show an extremely low overpotential of ca. 218 mV at 10 mA cm-2, which is superior to that of the state-of-the-art OER electrocatalysts. Using MoS2/Ni3S2heterostructures as bifunctional electrocatalysts, an alkali electrolyzer delivers a current density of 10 mA cm-2at a very low cell voltage of ca. 1.56 V. In combination with DFT calculations, this study demonstrates that the constructed interfaces synergistically favor the chemisorption of hydrogen and oxygen-containing intermediates, thus accelerating the overall electrochemical water splitting. | - |
dc.language | eng | - |
dc.relation.ispartof | Angewandte Chemie - International Edition | - |
dc.subject | electrocatalysts | - |
dc.subject | interface engineering | - |
dc.subject | molybdenum disulfide | - |
dc.subject | nickel sulfide | - |
dc.subject | water splitting | - |
dc.title | Interface Engineering of MoS<inf>2</inf>/Ni<inf>3</inf>S<inf>2</inf>Heterostructures for Highly Enhanced Electrochemical Overall-Water-Splitting Activity | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/anie.201602237 | - |
dc.identifier.scopus | eid_2-s2.0-84992297638 | - |
dc.identifier.volume | 55 | - |
dc.identifier.issue | 23 | - |
dc.identifier.spage | 6702 | - |
dc.identifier.epage | 6707 | - |
dc.identifier.eissn | 1521-3773 | - |