Journal Article FZJ-2022-02171

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Enhanced Polysulfide Conversion with Highly Conductive and Electrocatalytic Iodine‐Doped Bismuth Selenide Nanosheets in Lithium–Sulfur Batteries

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2022
Wiley-VCH Weinheim

Advanced functional materials 32(26), 2200529 - () [10.1002/adfm.202200529]

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Abstract: The shuttling behavior and sluggish conversion kinetics of intermediate lithium polysulfides (LiPS) represent the main obstacles to the practical application of lithium–sulfur batteries (LSBs). Herein, an innovative sulfur host is proposed, based on an iodine-doped bismuth selenide (I-Bi2Se3), able to solve these limitations by immobilizing the LiPS and catalytically activating the redox conversion at the cathode. The synthesis of I-Bi2Se3 nanosheets is detailed here and their morphology, crystal structure, and composition are thoroughly. Density-functional theory and experimental tools are used to demonstrate that I-Bi2Se3 nanosheets are characterized by a proper composition and micro- and nano-structure to facilitate Li+ diffusion and fast electron transportation, and to provide numerous surface sites with strong LiPS adsorbability and extraordinary catalytic activity. Overall, I-Bi2Se3/S electrodes exhibit outstanding initial capacities up to 1500 mAh g−1 at 0.1 C and cycling stability over 1000 cycles, with an average capacity decay rate of only 0.012% per cycle at 1 C. Besides, at a sulfur loading of 5.2 mg cm−2, a high areal capacity of 5.70 mAh cm−2 at 0.1 C is obtained with an electrolyte/sulfur ratio of 12 µL mg−1. This work demonstrated that doping is an effective way to optimize the metal selenide catalysts in LSBs.

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Contributing Institute(s):
  1. Physik Nanoskaliger Systeme (ER-C-1)
Research Program(s):
  1. 5351 - Platform for Correlative, In Situ and Operando Characterization (POF4-535) (POF4-535)
  2. ESTEEM3 - Enabling Science and Technology through European Electron Microscopy (823717) (823717)

Appears in the scientific report 2022
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 Record created 2022-05-16, last modified 2023-01-23


Published on 2022-03-23. Available in OpenAccess from 2023-03-23.:
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