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

Yanna Guo, Jing Tang, Huayu Qian, Zhongli Wang, Yusuke Yamauchi

Research output: Contribution to journalArticlepeer-review

241 Citations (Scopus)

Abstract

Herein, we present a facile metal-organic framework-engaged strategy to synthesize hollow Co3S4@MoS2 heterostructures as efficient bifunctional catalysts for both H2 and O2 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 Co3S4@MoS2 heterostructures are finally obtained after subsequent thermal annealing under a N2 atmosphere. Due to the synergistic effects between the hydrogen evolution reaction active catalyst of MoS2 and the oxygen evolution reaction active catalyst of Co3S4, the obtained hollow Co3S4@MoS2 heterostructures exhibit outstanding bifunctional catalytic performances toward both hydrogen and oxygen evolution reactions in acidic and alkaline media.

Original languageEnglish
Pages (from-to)5566-5573
Number of pages8
JournalChemistry of Materials
Volume29
Issue number13
DOIs
Publication statusPublished - 2017 Jul 11

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)
  • Materials Chemistry

Fingerprint Dive into the research topics of 'One-Pot Synthesis of Zeolitic Imidazolate Framework 67-Derived Hollow Co<sub>3</sub>S<sub>4</sub>@MoS<sub>2</sub> Heterostructures as Efficient Bifunctional Catalysts'. Together they form a unique fingerprint.

Cite this