Study on the Directional Synthesis of Bi <sub>2</sub> S <sub>3</sub> Induced by Graphene and the Mechanism of Pseudocapacitive Kinetics Regulation at the Interface
To address the issues of capacity decay and poor rate performance of Bi<sub>2</sub>S<sub>3</sub> anode materials, which are caused by their intrinsically low conductivity and significant volume expansion during cycling, this study adopts a redox self-assembly strategy. Under mild hydrothermal conditions, oxygen-containing functional groups on the surface of graphene oxide (GO) induce the directed growth of Bi<sub>2</sub>S<sub>3</sub> along the [001] crystallographic direction, successfully constructing a Bi<sub>2</sub>S<sub>3</sub>/GO composite anode with strong interfacial coupling. This structure effectively suppresses the agglomeration of Bi<sub>2</sub>S<sub>3</sub> nanorods, forms a 3D conductive network, alleviates volume strain, and avoids structural damage caused by traditional high-temperature sulfidation processes. Electrochemical tests show that the 1.0-Bi<sub>2</sub>S<sub>3</sub>/GO composite retains a capacity of 300 mAh·g<sup>-1</sup> after 100 cycles at a current density of 100 mA·g<sup>-1</sup>. At a high rate of 5000 mA·g<sup>-1</sup>, it still exhibits a reversible capacity of 198.62 mAh·g<sup>-1</sup>, and after current recovery, the capacity rapidly increases to 439 mAh·g<sup>-1</sup>, with a capacity retention rate exceeding 70%. The lithium-ion diffusion coefficient reaches 8.7×10<sup>-1</sup> <sup>2</sup> cm<sup>2</sup>·s<sup>-1</sup>, which is 2.8 times higher than that of the pure phase. Mechanistic analysis reveals that the characteristic peak (τ = 0.3 s) in the distribution relaxation time (DRT) relaxation spectrum corresponds to the pseudocapacitive behavior on the GO surface, with a contribution rate of 58% at a scan rate of 2 mV·s<sup>-1</sup>, significantly optimizing the ion storage dynamics at the interface. Additionally, the built-in electric field at the interface facilitates charge transfer, effectively shortening the relaxation time. The synergistic π-π stacking buffering network further enhances structural stability and reaction reversibility. This study, through the "directed growth-pseudocapacitance regulation-relaxation matching" triple mechanism, provides new insights for the design of high-performance sulfide-based anodes.
Authors
- T. Chen
- Zhicheng Ju (ORCID: https://orcid.org/0000-0002-2562-5774)
- Jian Ying Qi
- Zheng Xing (ORCID: https://orcid.org/0000-0002-0915-1820)
- Xinran Gao
- Runzhu Cui
- Fulin Zhu
- Yiming Jiang
- Lijuan Qian
- Mingtao Lu
Institutions
- China University of Mining and Technology (CN)
- Binzhou Technician College (CN)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2026-01-16
- DOI
- https://doi.org/10.1002/chem.202503274
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00