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Influence of Monolayered RuO<sub>2</sub> Nanosheets and Co<sup>2+</sup> Ion Linkers in Improving the Electrocatalytic Performance of MoS<sub>2</sub> Nanoflowers

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posted on 2022-06-01, 16:06 authored by Haslinda Binti Mohd Sidek, So Yeon Yun, Xiaoyan Jin, Seong-Ju Hwang
Hybridization between low-dimensional nanostructures has received considerable research interest, owing to its usefulness in the exploration of energy-efficient functional materials. In the present study, an effective method to synthesize high-performance electrocatalysts was established by employing monolayered two-dimensional RuO<sub>2</sub> nanosheets and Co<sup>2+</sup> ions as conductive additives and linker species, respectively. Intimately coupled hybrid electrocatalysts of Co–MoS<sub>2</sub>–RuO<sub>2</sub> were synthesized through the self-assembly of isocharged MoS<sub>2</sub> nanoflowers and RuO<sub>2</sub> nanosheets using oppositely charged Co<sup>2+</sup> linkers. Efficient interfacial charge transfer from RuO<sub>2</sub> nanosheets to MoS<sub>2</sub> nanostructures can be achieved via electrostatically driven strong electronic coupling between MoS<sub>2</sub>/RuO<sub>2</sub> nanostructures promoted by Co<sup>2+</sup> linkers. The co-incorporation of RuO<sub>2</sub> nanosheets and Co<sup>2+</sup> ion linkers was found to be considerably effective for optimization of the electrocatalyst performance and electrochemical stability of MoS<sub>2</sub> nanoflowers for the hydrogen evolution reaction in acidic and alkaline electrolytes. The beneficial roles of RuO<sub>2</sub> nanosheets and Co<sup>2+</sup> ions in the optimization of the electrocatalyst performance were attributable to the improvement of electrocatalysis kinetics, the expansion of the electrochemical active surface area, and the promotion of charge transport upon hybridization.

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