JOURNAL ARTICLE

Metal–Organic-Framework-Derived Hollow CoS<sub><i>x</i></sub>@MoS<sub>2</sub> Microcubes as Superior Bifunctional\nElectrocatalysts for Hydrogen Evolution and Oxygen Evolution Reactions

Abstract

Electrocatalytic\nwater-splitting catalysts play important roles\nin clean energy conversion systems. Herein, metal–organic framework-derived\n(MOF-derived) hollow CoS<sub><i>x</i></sub>@MoS<sub>2</sub> microcubes were successfully synthesized by a novel method. Co-MOF\n[(CH<sub>3</sub>)<sub>2</sub>NH<sub>2</sub>]­[Co­(HCOO)<sub>3</sub>]\nprepared by a simple liquid precipitation method at room temperature\nreacted with S<sup>2–</sup> released from thioacetamide (TAA)\nto generate Co<sub>9</sub>S<sub>8</sub> under solvothermal conditions. Through hydrothermal treatment,\nnumerous MoS<sub>2</sub> nanosheets grew on the surface of CoS<sub><i>x</i></sub> vertically and uniformly after introduction\nof sulfur and molybdenum sources, finally generating CoS<sub><i>x</i></sub>@MoS<sub>2</sub> heterostructures. As bifunctional\nelectrocatalysts, the heterostructures exhibited remarkable performance\nfor the hydrogen evolution reaction with a low overpotential of 239\nmV when the current density increased up to 10 mA cm<sup>–2</sup> and a small Tafel slope of 103 mV dec<sup>–1</sup> in 0.5\nM H<sub>2</sub>SO<sub>4</sub>. They also worked effectively for the\noxygen evolution reaction with a low overpotential of 347 mV at 10\nmA cm<sup>–2</sup> in 1 M KOH. The enhanced electrocatalytic\nactivities of CoS<sub><i>x</i></sub>@MoS<sub>2</sub> can\nbe ascribed to their unique heterostructures and the synergism between\nCoS<sub><i>x</i></sub> and MoS<sub>2</sub>.

Keywords:
Overpotential Oxygen evolution Tafel equation Catalysis Molybdenum Water splitting Precipitation Hydrothermal circulation

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