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One-Pot Synthesis of Zeolitic Imidazolate Framework 67-Derived Hollow Co3S4@MoS2 Heterostructures as Efficient Bifunctional Catalysts

journal contribution
posted on 2024-11-16, 02:58 authored by Yanna Guo, Jing Tang, Huayu Qian, Zhongli Wang, Yusuke Yamauchi
Herein, we present a facile metal-organic framework-engaged strategy to synthesize hollow Co 3 S 4 @MoS 2 heterostructures as efficient bifunctional catalysts for both H 2 and O 2 generation. The well-known cobalt-based metal-organic zeolitic imidazolate frameworks (ZIF-67) are used not only as the morphological template but also as the cobalt precursor. During the two-step temperature-raising hydrothermal process, ZIF-67 polyhedrons are first transformed to hollow cobalt sulfide polyhedrons by sulfidation, and then molybdenum disulfide nanosheets further grow and deposit on the surface of hollow cobalt sulfide polyhedrons at the increased temperature. The crystalline hollow Co 3 S 4 @MoS 2 heterostructures are finally obtained after subsequent thermal annealing under a N 2 atmosphere. Due to the synergistic effects between the hydrogen evolution reaction active catalyst of MoS 2 and the oxygen evolution reaction active catalyst of Co 3 S 4 , the obtained hollow Co 3 S 4 @MoS 2 heterostructures exhibit outstanding bifunctional catalytic performances toward both hydrogen and oxygen evolution reactions in acidic and alkaline media.

Funding

All-Metal Nanoporous Materials as Highly Active Electrocatalysts

Australian Research Council

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History

Citation

Guo, Y., Tang, J., Qian, H., Wang, Z. & Yamauchi, Y. (2017). One-Pot Synthesis of Zeolitic Imidazolate Framework 67-Derived Hollow Co3S4@MoS2 Heterostructures as Efficient Bifunctional Catalysts. Chemistry of Materials, 29 (13), 5566-5573.

Journal title

Chemistry of Materials

Volume

29

Issue

13

Pagination

5566-5573

Language

English

RIS ID

115223

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