Constructing Heterogeneous Structure in Metal-Organic Framework-Derived Hierarchical Sulfur Hosts for Capturing Polysulfides and Promoting Conversion Kinetics.
basic_science · Level V
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- Record sourced from PubMed, PMID 34694767.
- Also identified by DOI 10.1021/acsnano.1c07820.
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Abstract
Lithium-sulfur batteries (LSBs) are still severely blocked by the shuttle of polysulfides (LiPSs), resulting in low sulfur utilization and decreased lifetime. The optimal design of hosts with tailored porous structures and catalytic sites is expected to address this issue. Herein, a Bi/Bi<sub>2</sub>O<sub>3</sub> heterostructure within the metal-organic framework (MOF)-derived sulfur host with a hierarchical structure was elaborated for both serving as sulfur hosts and promoting the redox reaction kinetics of LiPSs. The shuttle effects of LiPSs can be mitigated by the dual functional Bi/Bi<sub>2</sub>O<sub>3</sub> heterostructure enriched in the outer layer of CAU-17-derived carbonic rods, <i>i</i>.<i>e</i>., the effective redox conversion of LiPSs can be realized at the Bi/Bi<sub>2</sub>O<sub>3</sub> heterointerface by the adsorption of LiPSs over Bi<sub>2</sub>O<sub>3</sub> and subsequently catalytic conversion over Bi. Benefiting from these merits, the fabricated LSBs realized a significantly optimized performance, including a high discharge capacity of 740.8 mAh g<sup>-1</sup> after 1000 cycles with an ultralow decay rate of 0.022% per cycle at 1 C, a high areal capacity of 6.6 mAh cm<sup>-2</sup> after 100 cycles with a sulfur loading of 8.1 mg cm<sup>-2</sup>, and good performance in pouch cells as well.