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Introduction of SnS2 to Regulate the Ferrous Disulfide Phase Evolution for the Construction of Triphasic Heterostructures Enabling Kinetically Accelerated and Durable Sodium Storage

  • Zibo Zhao
  • , Guang Sun*
  • , Yiming Zhang
  • , Ran Hua
  • , Xiting Wang
  • , Naiteng Wu*
  • , Jin Li
  • , Guilong Liu
  • , Donglei Guo
  • , Ang Cao
  • , Xianming Liu
  • , Hongshuai Hou*
  • *Corresponding author for this work
  • Henan Polytechnic University
  • Luoyang Normal University

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Transition metal sulfides (TMSs) still confront the challenges of capacity fading and inferior fast-charging capability for sodium storage. The rational design of heterostructures enables a new approach to conquer these drawbacks. In this work, a hierarchical structure consisting of SnS2 nanosheets and FeS2 microrods with triphasic heterostructures is proposed by the facile secondary growth and sulfidation process. The introduction of tin sources regulates the proportion of pyrite and marcasite phases, thereby achieving the triphasic heterostructures comprising pyrite, marcasite FeS2, and SnS2. When served as anode material for sodium-ion batteries, the optimized sample exhibits a high reversible capacity (901 mAh g−1) and durable cycling performances (827 mAh g−1 after 200 cycles at 1 A g−1 and 742 mAh g−1 after 700 cycles at 5 A g−1). Paring with the commercial Na3V2(PO3)3 cathodes, the full-cell also delivers extraordinary cyclic stability with a high capacity of 618 mAh g−1 (based on the weight of anode material) after 200 cycles at 1 A g−1 (98.7% capacity retention). The hierarchical structure with adjustably triphasic heterogeneous interfaces alleviates the volumetric expansion and interfacial passivation of active material, while modulating the energy band structure and inducing the build-in electric fields to boost Na+/electrons transport rate.
Original languageEnglish
Article number2314679
JournalAdvanced Functional Materials
Volume34
Issue number21
Number of pages10
ISSN1616-301X
DOIs
Publication statusPublished - 2024

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