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Design of the 1D/2D Bi2S3/Bi2O2S Heterojunction as Battery-Type Cathode Materials for Hybrid Supercapacitors

  • Wenju Wu
  • , Chao Gu
  • , Gang Liu*
  • , Xinmei Liu*
  • , Limin Dong*
  • , Dongbo Wang*
  • , Yuewu Huang
  • , Jingzhou Zhang
  • , Yuhan Li
  • , Fei Li
  • , Qianshi Wang
  • , Mingyang Wu
  • , Liancheng Zhao*
  • *Corresponding author for this work
  • Harbin University of Science and Technology
  • Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

This research accomplished the controlled fabrication of a 1D/2D Bi2S3/Bi2O2S heterostructure for hybrid supercapacitor applications, where Bi2S3 nanorods were grown on Bi2O2S nanosheets to form the composite material. When the ratio of Bi2S3 to Bi2O2S is controlled at 5:3, the composite material demonstrates outstanding electrochemical properties. This is due to the appropriate content of Bi2O2S, which helps construct a good interface and enhance ion diffusion capability, thereby improving the electrochemical kinetics. The strategic combination of Bi2S3’s theoretical capacity and Bi2O2S’s structural stability yields a composite material with remarkable electrochemical properties, including enhanced reversible capacity and minimized polarization during cycling. Specifically, the Bi2S3/Bi2O2S-60 electrode delivers outstanding specific capacities of 1076.6 C g–1 at 1 A g–1 and maintains 730.3 C g–1 at 10 A g–1, demonstrating excellent rate capability. Notably, the composite exhibits significantly improved cycling stability (82.8% capacity retention after 10,000 cycles at 10 A g–1) compared to pure Bi2S3(67.4%) and Bi2O2S (73.6%). When configured as a hybrid supercapacitor (Bi2S3/Bi2O2S-60//AC), the device achieves an impressive energy density of 68.28 Wh kg–1 (810.73 W kg–1) with exceptional long-term stability (93.5% capacity retention after 10,000 cycles). The coherent interface studied in this paper brings a new perspective to the field of supercapacitors.

Original languageEnglish
Pages (from-to)5509-5522
Number of pages14
JournalCrystal Growth and Design
Volume25
Issue number14
DOIs
StatePublished - 16 Jul 2025

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