Heterostructure of reduced graphene oxide supported tin (IV) sulfide nanopetals as an anode material for Sodium/Potassium-ion batteries: Evidence for the formation of C-S bond

石墨烯 阳极 氧化物 硫化物 电解质 材料科学 电化学 无机化学 化学工程 复合数 化学 纳米技术 复合材料 电极 冶金 物理化学 工程类
作者
C. Nithya,S. Dhanushree,Indu Elizabeth,Kriti Tyagi,P Bavya
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:492: 144347-144347 被引量:2
标识
DOI:10.1016/j.electacta.2024.144347
摘要

Anodes that engage in conversion as well as alloying reactions are highly attractive candidates for sodium/potassium-ion batteries (SIBs and PIBs) because of their high theoretical specific capacities. Herein, Tin sulphide@reduced graphene oxide (SnS2 nanopetal@rGO) composite material is investigated as an advanced anode material for SIBs and PIBs. In this work, a simple hydrothermal synthesis of ultrathin SnS2 nanopetals covalently decorated on the surface of rGO is demonstrated as an anode material for SIBs and PIBs. The as prepared SnS2@rGO displays an initial charge capacity of 749 (at 0.2 A g−1) and 852 mAh g−1 (at 0.1 A g−1) for SIBs and PIBs respectively. The SnS2@rGO hybrid exhibited excellent cycle life which is attributed to the introduction of rGO in the composite as well as the in-built formed C-S bond. Moreover, the rGO matrix, firmly anchored with C–S bonds, envelops the outer SnS2, effectively inhibiting direct contact between SnS2 and the electrolyte. These combined effects contribute to impede the irreversible conversion of sulfur to sulfite, thus ensuring excellent structural stability throughout electrochemical cycling. The well-engineered nanoarchitecture not only guarantees the fast electrode kinetics, but also confirms excellent pseudo capacitance contribution during repetitive cycles which is confirmed by kinetic studies. Thus, SnS2@rGO is found to be a most promising electrode for sodium/potassium-ion batteries.
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