Boosting bidirectional conversion of polysulfide driven by the built-in electric field of MoS <sub>2</sub>/MoP Mott–Schottky heterostructures in lithium–sulfur batteries
Meixiu Song, Yanan Liu, Jingzhe Hong, Xiaoshuang Wang, Xiaoxiao Huang
Abstract
Heterostructure engineering for sulfur hosts is an effective way to achieve interfacial synergistic effects on suppressing the “shuttle effect” of polysulfides and thus improve the electrochemical performance of lithium-sulfur (Li-S) batteries. Rational selection and design of different components into heterostructures is vital to enhance the synergistic effect. Herein, MoS<sub>2</sub>/MoP Mott-Schottky heterostructures nanoparticles decorated on reduced graphene oxide (MoS<sub>2</sub>/MoP@rGO) are fabricated, and used as sulfur host firstly. Theoretical calculation and experiment results reveal that in-situ introduction of MoP could tune the electronic structure and activate the basal plane of MoS<sub>2</sub>, and achieve the interfacial synergistic effects between adsorption (MoS<sub>2</sub>) and fast conversion (MoP). Such synergistic effects enable MoS<sub>2</sub>/MoP@rGO to not only remarkably facilitate the Li<sub>2</sub>S deposition during discharging process but also significantly accelerate the Li<sub>2</sub>S dissolution during charging process, demonstrating bidirectional promotion behaviors. Thus, the designed cathode delivers an initial capacity of 919.5 mAh g<sup>-1</sup> with a capacity of 502.3 mAh g<sup>-1</sup> remaining after 700 cycles at 0.5 C. Even under a higher sulfur loading of 4.31 mg cm<sup>-2</sup> and a lower E/S of 8.21 μL mg<sup>-1</sup>, the MoS<sub>2</sub>/MoP@rGO@S cathode could still achieve good capacity and cycle stability. This work provides a novel and efficient structural design strategy of sulfur hosts for high-performance Li-S energy storage systems.