Mastering Surface Sulfidation of MnP‐MnO2 Heterostructure to Facilitate Efficient Polysulfide Conversion in Li─S Batteries

Abstract

Abstract The development of lithium–sulfur (Li─S) batteries has been hampered by the shuttling effect of lithium polysulfides (LiPSs). An effective method to address this issue is to use an electrocatalyst to accelerate the catalytic conversion of LiPSs. In this study, heterogeneous MnP‐MnO2 nanoparticles are uniformly synthesized and embedded in porous carbon (MnP‐MnO2/C) as core catalysts to improve the reaction kinetics of LiPSs. In situ characterization and density functional theory (DFT) calculations confirm that the MnP‐MnO2 heterostructure undergo surface sulfidation during the charge/discharge process, forming the MnS2 phase. Surface sulfidation of the MnP‐MnO2 heterostructure catalyst significantly accelerated the SRR and Li2S activation, effectively inhibiting the LiPSs shuttling effect. Consequently, the MnP‐MnO2/C@S cathode achieves outstanding rate performance (10 C, 500 mAh g−1) and ultrahigh cycling stability (0.017% decay rate per cycle for 2000 cycles at 5 C). A pouch cell with MnP‐MnO2/C@S cathode delivers a high energy density of 429 Wh kg−1. This study may provide a new approach to investigating the surface sulfidation of electrocatalysts, which is valuable for advancing high‐energy‐density Li−S batteries.

Keywords

• heterostructure
• in situ characterization
• lithium–sulfur batteries
• manganese phosphide
• surface sulfidation