P-block element modulated 1 T phase MoS<sub>2</sub> with Ru lattice grafting for high-performance Li | |O<sub>2</sub> batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39920107.
- Also identified by DOI 10.1038/s41467-024-55073-5 and PMC identifier 11806026.
- Licence recorded as CC BY-NC-ND.
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Abstract
The metallic phase MoS<sub>2</sub> (1T-MoS<sub>2</sub>) supported metal-nanocatalyst is an appealing material system for accelerating the redox kinetics of non-aqueous Li | |O<sub>2</sub> batteries. However, the drawbacks associated with the surface orbital steric effect and the internal electron coupling results in a detrimental effect for the stability of 1T-MoS<sub>2</sub>, especially for the interface charge transfer. This makes it difficult to incorporate guest metal nanoparticles without compromising the 1 T phase support. To circumvent these issues, here we propose a p-block element (In-O) doping strategy to stabilize the 1 T phase MoS<sub>2</sub> by moderating the surface orbital steric effect and strengthening the internal chemical bonding, and thus for the epitaxial Ru nanocatalyst graft on the stabilized 1T-MoS<sub>2</sub> for Li | |O<sub>2</sub> batteries. The experimental and theoretical analyzes indicate that the In-O-MoS<sub>2</sub>@Ru enhances the O<sub>2</sub> dissociation and facilitates the adsorption of LiO<sub>2</sub> intermediates. This effect promotes the growth of weakly crystalline Li<sub>2</sub>O<sub>2</sub> films during oxygen reduction reaction, which can be more easily decomposed during the oxygen evolution reaction, thereby enhancing the bifunctional-catalytic kinetics. When employed at the positive electrode for non-aqueous Li | |O<sub>2</sub> batteries, In-O-MoS<sub>2</sub>@Ru shows an overpotential of 0.37 V and a cycling life of 284 cycles at 200 mA g<sup>-1</sup> with a final discharge specific capacity of 1000 mAh g<sup>-1</sup> at 25 °C.