Coupling Nonstoichiometric Zn0.76Co0.24S with NiCo2S4 Composite Nanoflowers for Efficient Synergistic Electrocatalytic Oxygen and Hydrogen Evolution Reactions
Transition-metal sulfide-based composite nanomaterials have garnered extensive interest not only for their unique morphological architectures but also for exploring as a noble-metal-free cost-effective, durable, and highly stable catalyst for electrochemical water splitting. In this work, we synthes...
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Published in | Energy & fuels Vol. 37; no. 1; pp. 604 - 613 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
05.01.2023
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Subjects | |
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Abstract | Transition-metal sulfide-based composite nanomaterials have garnered extensive interest not only for their unique morphological architectures but also for exploring as a noble-metal-free cost-effective, durable, and highly stable catalyst for electrochemical water splitting. In this work, we synthesized in situ nonstoichiometric Zn0.76Co0.24S with NiCo2S4 binary composite flowers (Zn0.76Co0.24S/NiCo2S4) in one step by thermal decomposition of Zn2[PDTC]4 and Ni[PDTC]2 complexes by a solvothermal process in a nonaqueous medium from their molecular precursor, and their potential application in electrochemical oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) was investigated. Field-emission scanning electron microscopy and transmission electron microscopy analyses revealed the flower-shaped morphology of as-synthesized Zn0.76Co0.24S/NiCo2S4. Again, the structural and chemical compositions were confirmed through powder X-ray diffraction and X-ray photoelectron spectroscopy studies, respectively. The as-obtained 3D flower-type Zn0.76Co0.24S/NiCo2S4 nanostructure was further subject to electrochemical OER and HER in alkaline and acidic media, respectively. Zn0.76Co0.24S/NiCo2S4 showed low overpotential values of 248 mV (Tafel slope, 85 mV dec–1) and 141 mV (Tafel slope, 79 mV dec–1) for OER and HER activities, respectively, due to the synergistic effects of Zn0.76Co0.24S and NiCo2S4. Several long-term stability tests also affirmed that the Zn0.76Co0.24S/NiCo2S4 composite nanostructure is a highly stable and efficient electrocatalyst toward OER and HER activities as compared to the recently reported superior bifunctional electrocatalysts as well as state-of-the-art materials. |
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AbstractList | Transition-metal sulfide-based composite nanomaterials have garnered extensive interest not only for their unique morphological architectures but also for exploring as a noble-metal-free cost-effective, durable, and highly stable catalyst for electrochemical water splitting. In this work, we synthesized in situ nonstoichiometric Zn0.₇₆Co0.₂₄S with NiCo₂S₄ binary composite flowers (Zn₀.₇₆Co₀.₂₄S/NiCo₂S₄) in one step by thermal decomposition of Zn₂[PDTC]₄ and Ni[PDTC]₂ complexes by a solvothermal process in a nonaqueous medium from their molecular precursor, and their potential application in electrochemical oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) was investigated. Field-emission scanning electron microscopy and transmission electron microscopy analyses revealed the flower-shaped morphology of as-synthesized Zn₀.₇₆Co₀.₂₄S/NiCo₂S₄. Again, the structural and chemical compositions were confirmed through powder X-ray diffraction and X-ray photoelectron spectroscopy studies, respectively. The as-obtained 3D flower-type Zn₀.₇₆Co₀.₂₄S/NiCo₂S₄ nanostructure was further subject to electrochemical OER and HER in alkaline and acidic media, respectively. Zn₀.₇₆Co₀.₂₄S/NiCo₂S₄ showed low overpotential values of 248 mV (Tafel slope, 85 mV dec–¹) and 141 mV (Tafel slope, 79 mV dec–¹) for OER and HER activities, respectively, due to the synergistic effects of Zn₀.₇₆Co₀.₂₄S and NiCo₂S₄. Several long-term stability tests also affirmed that the Zn₀.₇₆Co₀.₂₄S/NiCo₂S₄ composite nanostructure is a highly stable and efficient electrocatalyst toward OER and HER activities as compared to the recently reported superior bifunctional electrocatalysts as well as state-of-the-art materials. Transition-metal sulfide-based composite nanomaterials have garnered extensive interest not only for their unique morphological architectures but also for exploring as a noble-metal-free cost-effective, durable, and highly stable catalyst for electrochemical water splitting. In this work, we synthesized in situ nonstoichiometric Zn0.76Co0.24S with NiCo2S4 binary composite flowers (Zn0.76Co0.24S/NiCo2S4) in one step by thermal decomposition of Zn2[PDTC]4 and Ni[PDTC]2 complexes by a solvothermal process in a nonaqueous medium from their molecular precursor, and their potential application in electrochemical oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) was investigated. Field-emission scanning electron microscopy and transmission electron microscopy analyses revealed the flower-shaped morphology of as-synthesized Zn0.76Co0.24S/NiCo2S4. Again, the structural and chemical compositions were confirmed through powder X-ray diffraction and X-ray photoelectron spectroscopy studies, respectively. The as-obtained 3D flower-type Zn0.76Co0.24S/NiCo2S4 nanostructure was further subject to electrochemical OER and HER in alkaline and acidic media, respectively. Zn0.76Co0.24S/NiCo2S4 showed low overpotential values of 248 mV (Tafel slope, 85 mV dec–1) and 141 mV (Tafel slope, 79 mV dec–1) for OER and HER activities, respectively, due to the synergistic effects of Zn0.76Co0.24S and NiCo2S4. Several long-term stability tests also affirmed that the Zn0.76Co0.24S/NiCo2S4 composite nanostructure is a highly stable and efficient electrocatalyst toward OER and HER activities as compared to the recently reported superior bifunctional electrocatalysts as well as state-of-the-art materials. |
Author | Biswas, Rathindranath Thakur, Pooja Patil, Ranjit A. Rom, Tanmay Som, Shubham Ahmed, Imtiaz Kumar, Bhupender Ali, Mir Sahidul Ma, Yuan-Ron Paul, Avijit Kumar Haldar, Krishna Kanta Chopra, Deepak |
AuthorAffiliation | Department of Chemistry Department of Polymer Science and Technology National Institute of Technology National Dong Hwa University Indian Institute of Science Education and Research Department of Physics School of Applied Material Sciences |
AuthorAffiliation_xml | – name: School of Applied Material Sciences – name: Department of Chemistry – name: National Institute of Technology – name: Department of Physics – name: National Dong Hwa University – name: Indian Institute of Science Education and Research – name: Department of Polymer Science and Technology |
Author_xml | – sequence: 1 givenname: Rathindranath orcidid: 0000-0002-0909-1442 surname: Biswas fullname: Biswas, Rathindranath organization: Department of Chemistry – sequence: 2 givenname: Pooja surname: Thakur fullname: Thakur, Pooja organization: Department of Chemistry – sequence: 3 givenname: Imtiaz orcidid: 0000-0002-8582-4484 surname: Ahmed fullname: Ahmed, Imtiaz organization: Department of Chemistry – sequence: 4 givenname: Tanmay orcidid: 0000-0001-5321-0069 surname: Rom fullname: Rom, Tanmay organization: National Institute of Technology – sequence: 5 givenname: Mir Sahidul surname: Ali fullname: Ali, Mir Sahidul organization: Department of Polymer Science and Technology – sequence: 6 givenname: Ranjit A. surname: Patil fullname: Patil, Ranjit A. organization: National Dong Hwa University – sequence: 7 givenname: Bhupender surname: Kumar fullname: Kumar, Bhupender organization: School of Applied Material Sciences – sequence: 8 givenname: Shubham surname: Som fullname: Som, Shubham organization: Indian Institute of Science Education and Research – sequence: 9 givenname: Deepak orcidid: 0000-0002-0018-6007 surname: Chopra fullname: Chopra, Deepak organization: Indian Institute of Science Education and Research – sequence: 10 givenname: Avijit Kumar surname: Paul fullname: Paul, Avijit Kumar organization: National Institute of Technology – sequence: 11 givenname: Yuan-Ron orcidid: 0000-0002-7048-953X surname: Ma fullname: Ma, Yuan-Ron organization: National Dong Hwa University – sequence: 12 givenname: Krishna Kanta orcidid: 0000-0002-0675-8299 surname: Haldar fullname: Haldar, Krishna Kanta email: krishankant.haldar@cup.edu.in organization: Department of Chemistry |
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SubjectTerms | Catalysis and Kinetics catalysts cost effectiveness electrochemistry energy hydrogen production nanoflowers oxygen oxygen production thermal degradation transmission electron microscopy X-ray diffraction X-ray photoelectron spectroscopy |
Title | Coupling Nonstoichiometric Zn0.76Co0.24S with NiCo2S4 Composite Nanoflowers for Efficient Synergistic Electrocatalytic Oxygen and Hydrogen Evolution Reactions |
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