Covalent Coupling-Stabilized Transition-Metal Sulfide/Carbon Nanotube Composites for Lithium/Sodium-Ion Batteries

Tianyi Hou, Borui Liu, Xiaohong Sun*, Anran Fan, Zhongkai Xu, Shu Cai, Chunming Zheng*, Guihua Yu, Antonio Tricoli*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    131 Citations (Scopus)

    Abstract

    Transition-metal sulfides (TMSs) powered by conversion and/or alloying reactions are considered to be promising anode materials for advanced lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). However, the limited electronic conductivity and large volume expansion severely hinder their practical application. Herein, we report a covalent coupling strategy for TMS-based anode materials using amide linkages to bind TMSs and carbon nanotubes (CNTs). In the synthesis, the thiourea acts as not only the capping agent for morphology control but also the linking agent for the covalent coupling. As a proof of concept, the covalently coupled ZnS/CNT composite (CC-ZnS/CNT) has been prepared, with ZnS nanoparticles (μ10 nm) tightly anchored on CNT bundles. The compact ZnS-CNT heterojunctions are greatly beneficial to facilitating the electron/ion transfer and ensuring structural stability. Due to the strong coupling interaction between ZnS and CNTs, the composite presents prominent pseudocapacitive behavior and highly reversible electrochemical processes, thus leading to superior long-term stability and excellent rate capability, delivering reversible capacities of 333 mAh g-1 at 2 A g-1 over 4000 cycles for LIBs and 314 mAh g-1 at 5 A g-1 after 500 cycles for SIBs. Consequently, CC-ZnS/CNT exhibits great competence for applications in LIBs and SIBs, and the covalent coupling strategy is proposed as a promising approach for designing high-performance anode materials.

    Original languageEnglish
    Pages (from-to)6735-6746
    Number of pages12
    JournalACS Nano
    Volume15
    Issue number4
    DOIs
    Publication statusPublished - 27 Apr 2021

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