Mn<sup>2+</sup>-Doped MoS<sub>2</sub>/MXene Heterostructure Composites as Cathodes for Aqueous Zinc-Ion Batteries
Wen Yang, Lianshan Mou, Baoquan Xiao, Jie Chen, Di Wang, Shanglong Peng, Juanjuan Huang
Abstract
Typical layered transition-metal chalcogenide materials, especially MoS 2, are gradually attracting widespread attention as aqueous Zn-ion battery (AZIB) cathode materials by virtue of their two-dimensional structure, tunable band gap, and abundant edges. The metastable phase 1T-MoS 2 exhibits better electrical conductivity, electrochemical activity, and zinc storage capacity compared to the thermodynamically stable 2H-MoS 2 . However, 1T-MoS 2 is still limited by the phase stability and layered structure destruction for AZIB application. Thus, a three-dimensional interconnected network heterostructure (Mn-MoS 2 /MXene) consisting of Mn 2+ -doped MoS 2 and MXene with a high percentage of 1T phase (82.9%) was synthesized by hydrothermal methods and investigated as the cathode for AZIBs. It was found that S–Mn–S covalent bonds between MoS 2 interlayers and Ti–O–Mo bonds at heterogeneous interfaces can act as “electron bridges” to facilitate electron and charge transfer. And the doping of Mn 2+ and the combination of MXene not only expanded the interlayer spacing of MoS 2 but also maintained the metastable structure of 1T-MoS 2 nanosheets, acting to reduce the activation energy for Zn 2+ intercalation and enhance specific capacity. The obtained Mn-MoS 2 /MXene contains more 1T-MoS 2 and provides an improved specific capacity of 191.7 mAh g –1 at 0.1 A g –1 . Compared with Mn-MoS 2 and pure MoS 2, it also exhibits enhanced cycling stability with a capacity retention of 80.3% after 500 cycles at 1 A g –1 . Besides, the conductivity of Mn-MoS 2 /MXene is significantly improved, which induces a lower activation energy of the zinc ions during intercalation/deintercalation.