LAUSR

Multiple unfavorable features, such as poor electronic conductivity of sulfur cathodes, the dissolution and shuttling of sodium polysulfides (Na2Sn) in electrolytes, and the slower kinetics for the decomposition of solid Na2S, make sodium-sulfur batteries (NaSBs) impractical. To overcome these obstacles, novel double-transition metal (DTM) MXenes, Mo2TiC2T2, (T = O and S) are studied as an anchoring material (AM) to immobilize higher-order polysulfides and to expedite the otherwise slower kinetics of insoluble short-chain polysulfides. Density functional theory (DFT) calculations are carried out to justify and compare the effectiveness of Mo2TiC2S2 and Mo2TiC2O2 as AMs by analyzing their interactions with S8/Na2Sn (n = 1, 2, 4, 6, and 8). Mo2TiC2S2 provides moderate adsorption strength compared to Mo2TiC2O2, therefore, it is expected to effectively inhibit Na2Sn dissolution and shuttling without causing decomposition of Na2Sn. The calculated Gibbs free energies of the rate-determining step for sulfur reduction reactions (SRR) are found to be significantly lower (0.791 eV for S and 0.628 eV for O functionalization) than that in vacuum (1.442 eV), suggesting that the SRR is more thermodynamically favorable on Mo2TiC2T2 during discharge. Additionally, both Mo2TiC2S2 and Mo2TiC2O2 demonstrated effective electrocatalytic activity for the decomposition of Na2S, with a substantial reduction in the energy barrier to 1.59 eV for Mo2TiC2S2 and 1.67 eV for Mo2TiC2O2. While Mo2TiC2O2 had superior binding properties, structural distortion is observed in Na2Sn, which may adversely affect cyclability. On the other hand, because of its moderate binding energy, enhanced electronic conductivity, and significantly faster oxidative decomposition kinetics of polysulfides, Mo2TiC2S2 can be considered as an effective AM for suppressing the shuttle effect and improving the performance of NaSBs.