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
posted on 2022-06-01, 16:06authored byHaslinda
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.