TY - JOUR
T1 - One-Pot Synthesis of Zeolitic Imidazolate Framework 67-Derived Hollow Co3S4@MoS2 Heterostructures as Efficient Bifunctional Catalysts
AU - Guo, Yanna
AU - Tang, Jing
AU - Qian, Huayu
AU - Wang, Zhongli
AU - Yamauchi, Yusuke
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/7/11
Y1 - 2017/7/11
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85022330881&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.7b00867
DO - 10.1021/acs.chemmater.7b00867
M3 - Article
AN - SCOPUS:85022330881
SN - 0897-4756
VL - 29
SP - 5566
EP - 5573
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 13
ER -