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Heterogeneous Cr-doped Co3S4/NiMoS4 bifunctional electrocatalyst for efficient overall water splitting

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dc.title Heterogeneous Cr-doped Co3S4/NiMoS4 bifunctional electrocatalyst for efficient overall water splitting en
dc.contributor.author Li, Yiwen
dc.contributor.author Zhu, Zhengju
dc.contributor.author Zhong, Yu Lin
dc.contributor.author Jin, Yifan
dc.contributor.author Sáha, Petr
dc.contributor.author Cheng, Qilin
dc.relation.ispartof Journal of Power Sources
dc.identifier.issn 0378-7753 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2024
utb.relation.volume 614
dc.type article
dc.language.iso en
dc.publisher Elsevier B.V.
dc.identifier.doi 10.1016/j.jpowsour.2024.234969
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0378775324009212
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0378775324009212/pdfft?md5=23d4503edeb76f9ae046bb7e242f5196&pid=1-s2.0-S0378775324009212-main.pdf
dc.subject electrocatalytic water splitting en
dc.subject heterostructures en
dc.subject metal doping en
dc.subject metal sulfides en
dc.subject nanostructures en
dc.description.abstract Exploration of efficient and robust catalysts for electrocatalytic water splitting is paramount yet challenging for economical hydrogen production. Here, nanoforest-like heterostructures composed of inner NiMoS4 nanowires and outer Cr-doped Co3S4 nanosheets were grown on nickel foams (Cr–Co3S4/NiMoS4) as highly efficient bifunctional electrocatalysts. As a result, Cr–Co3S4/NiMoS4 heterostructures exhibit low overpotentials of 72 mV and 243 mV for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) at 10 mA cm−2, respectively. Moreover, the water electrolyzer assembled by Cr–Co3S4/NiMoS4 as bifunctional electrodes reaches 10 mA cm−2 at 1.587 V and maintains exceptional stability over 200 h. The experimental and theoretical characterizations collectively unveil that the charge redistribution occurs at the heterointerface between Cr-doped Co3S4 and NiMoS4, resulting in the regulation of both their electronic structures, which optimizes the adsorption of HER intermediates and decreases the energy barrier of determining step for OER. Additionally, the Cr doping and nanoforest-like morphology increase the intrinsic conductivity and the exposure of active sites, collectively improving the water electrolysis efficiency. This finding presents a promising way to construct and adjust the heterojunction engineering for bifunctional electrocatalysts toward water electrolysis. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1012048
utb.identifier.scopus 2-s2.0-85197089973
utb.identifier.coden JPSOD
utb.source j-scopus
dc.date.accessioned 2024-10-22T08:18:23Z
dc.date.available 2024-10-22T08:18:23Z
dc.description.sponsorship National Natural Science Foundation of China, NSFC, (22108079); National Natural Science Foundation of China, NSFC; Shanghai Pujiang Program, (21PJD018); China Postdoctoral Science Foundation, (2020M681208); China Postdoctoral Science Foundation
utb.ou Sino-EU Joint Laboratory of New Energy Materials and Devices
utb.contributor.internalauthor Sáha, Petr
utb.contributor.internalauthor Cheng, Qilin
utb.fulltext.sponsorship This work was supported by the National Natural Science Foundation of China (22108079), Shanghai Pujiang Program (21PJD018) and China Postdoctoral Science Foundation (2020M681208).
utb.scopus.affiliation Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China; Queensland Micro‐ and Nanotechnology Centre, School of Environment and Science, Griffith University, Nathan, 4111, QLD, Australia; Sino-EU Joint Laboratory of New Energy Materials and Devices, Tomas Bata University in Zlin, nam. T. G. Masaryka 5555, Zlin, 760 01, Czech Republic
utb.fulltext.projects 22108079
utb.fulltext.projects 21PJD018
utb.fulltext.projects 2020M681208
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