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dc.contributor.authorWang, Lin
dc.contributor.authorCao, Junhui
dc.contributor.authorCheng, Xiaodi
dc.contributor.authorLei, Chaojun
dc.contributor.authorDai, Qizhou
dc.contributor.authorYang, Bin
dc.contributor.authorLi, Zhongjian
dc.contributor.authorYounis, M Adnan
dc.contributor.authorLei, Lecheng
dc.contributor.authorHou, Yang
dc.contributor.authorOstrikov, Kostya
dc.date.accessioned2019-09-10T02:31:38Z
dc.date.available2019-09-10T02:31:38Z
dc.date.issued2019
dc.identifier.issn2168-0485
dc.identifier.doi10.1021/acssuschemeng.9b01315
dc.identifier.urihttp://hdl.handle.net/10072/387155
dc.description.abstractDevelopment of nonprecious metal-based electrocatalysts supporting hydrogen evolution reaction (HER) in the entire pH range has gained significant importance for harvesting green and renewable energy. Herein, we developed a novel electrocatalyst based on 3D carbon nanoarchitecture hybrid, which consists of CoP nanoparticles (CoP NPs) embedded into N-doped carbon nanotubes (NCNT), grafted on carbon polyhedron (CoP/NCNT-CP) that was prepared by carbonization and low-temperature phosphatization treatment of cobalt-based zeolite imidazole framework (ZIF). Benefiting from the strong synergistic effect and unique 3D structure, the CoP/NCNT-CP hybrid loaded on Ni foam exhibited excellent electrocatalytic HER performance in base with a low overpotential of 165 mV at a current density of 10 mA cm–2, which is competitive with the previously reported Co-based hybrid electrocatalysts. Furthermore, the CoP/NCNT-CP also demonstrated high HER electrocatalytic activities in both neutral and acidic conditions with the overpotentials of 203 and 305 mV at the current density of 10 mA cm–2. Additionally, the bifunctional CoP/NCNT-CP electrode simultaneously acted as an anode for hydrazine oxidation reaction (HzOR) and a cathode for HER. Excellent catalytic performance was demonstrated in base conditions with a low cell potential of 0.89 V at 10 mA cm–2, which was much lower than the voltage of overall water splitting (1.91 V) at the same current density.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofpagefrom10044
dc.relation.ispartofpageto10051
dc.relation.ispartofissue11
dc.relation.ispartofjournalACS Sustainable Chemistry and Engineering
dc.relation.ispartofvolume7
dc.subject.fieldofresearchAnalytical chemistry
dc.subject.fieldofresearchChemical engineering
dc.subject.fieldofresearchcode3401
dc.subject.fieldofresearchcode4004
dc.subject.keywordsScience & Technology
dc.subject.keywordsPhysical Sciences
dc.subject.keywordsTechnology
dc.subject.keywordsChemistry, Multidisciplinary
dc.subject.keywordsGreen & Sustainable Science & Technology
dc.titleZIF-Derived Carbon Nanoarchitecture as a Bifunctional pH-Universal Electrocatalyst for Energy-Efficient Hydrogen Evolution
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationWang, L; Cao, J; Cheng, X; Lei, C; Dai, Q; Yang, B; Li, Z; Younis, MA; Lei, L; Hou, Y; Ostrikov, K, ZIF-Derived Carbon Nanoarchitecture as a Bifunctional pH-Universal Electrocatalyst for Energy-Efficient Hydrogen Evolution, ACS Sustainable Chemistry and Engineering, 2019, 7 (11), pp. 10044-10051
dc.date.updated2019-09-10T02:30:01Z
gro.hasfulltextNo Full Text
gro.griffith.authorOstrikov, Ken


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