The dual modification of MXene hybridization and cut-off voltage adjustment endows MoS 2/Ti 3C 2T x with enhanced reaction kinetics and satisfactory electrochemical performance.
Molybdenum disulfide (MoS 2), a typical layered transition metal sulfide with a large interlayer distance, narrow band gap structure, and high theoretical capacity for sodium storage, shows tremendous promise for sodium-ion batteries (SIBs). Unfortunately, the inadequate cycling stability due to the mechanical failure caused by the deep conversion reaction upon cycling at low voltage, combined with its intrinsic poor electical conductivity, results in degraded electrochemical performance. In this work, a novel Ti 3C 2T x MXene was introduced to fabricate a MoS 2/Ti 3C 2T x hybrid through a facile hydrothermal approach, dramatically increasing the reaction kinetics of the hybrid electrode. Additionally, further increasing the discharge cut-off voltage to 0.2 V, the target MoS 2/Ti 3C 2T x exhibits remarkable sodium storage performance in terms of specific capacity, cyclability, and rate capability. Strikingly, the capacity hardly ever decays after 1000 cycles at 1.0 A g −1. Noteworthily, the impressive sodium storage performance of MoS 2/Ti 3C 2T x within 0.2–3.0 V originates from the effective avoidance of deep conversion reations below 0.2 V and improved electronic kinetics from the combination with Ti 3C 2T x flakes. Moreover, ex situ phase characteriztion, kinetic study, and pseudocapacitive effect for charge storage were also investigated to reveal the origin of the improved electrochemical performance. Importantly, the modifications of both electrode structure and cut-off voltage provide an effective way to optimize the electrochemical redox of the target electrode.