In-situ decoration of tin sulfide on Niobium carbide MXene with robust electronic coupling for improved sodium storage performance

Abstract

Tin sulfide (SnS) has been considered as one of the most promising sodium storage materials because of its excellent electrochemical activity, low cost, and low-dimensional structure. However, owing to the serious volume change upon discharging/charging and poor electronic conductivity, the SnS-based electrodes often suffer from electrode pulverization and sluggish reaction kinetics, thus resulting in serious capacity fading and degraded rate capability. In this work, SnS nanoparticles uniformly distributed on the surface of the layered Niobium carbide MXene (SnS/Nb2CTx) were fabricated through a facile solvothermal approach followed by calcination, endowing the SnS/Nb2CTx with a three-dimensional interconnected framework as well as fast charge transfer. Benefitting from the excellent electronic/ionic conductivity, efficient buffering matrix, abundant active sites, and high sodium storage activity inherited from the structure design, the robust electronic coupling between SnS nanoparticle and Nb2CTx MXene results in excellent electrochemical output, which demonstrates superior reversible capacities of 479.6 (0.1 A/g up to 100 cycles) and 278.9 mAh/g (0.5 A/g up to 500 cycles) upon sodium storage, respectively. The excellent electrochemical performance manifests the promise of the combination of metal sulfides with Nb2CTx MXene to fabricate high-performance electrodes for sodium storage.