Stable Na/K–S Batteries with Conductive Organosulfur Polymer Microcages as Cathodes

Na–S and K–S batteries, with high-energy density, using naturally more abundant and affordable metals compared with rare resources like Li, Co, and Ni elements, have inspired intense research interest. However, the sulfur cathodes for Na/K storage are plagued by soluble polysulfide shuttling, larger...

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Veröffentlicht in:Journal of the American Chemical Society 2025-01, Vol.147 (1), p.566-575
Hauptverfasser: Zeng, Xian, Yi, Zi-Jian, Zhu, Guo-Yu, Zhu, Ning-Ning, Chen, Yan-Fei, Xiao, Ji-Miao, Chen, Run-Hang, Yang, Menghua, Jin, Hongchang, Bin, De-Shan, Li, Dan
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Sprache:eng
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Zusammenfassung:Na–S and K–S batteries, with high-energy density, using naturally more abundant and affordable metals compared with rare resources like Li, Co, and Ni elements, have inspired intense research interest. However, the sulfur cathodes for Na/K storage are plagued by soluble polysulfide shuttling, larger volumetric deformation, and sluggish redox kinetics. Here, we report that a conductive organosulfur polymer microcage, fabricated facilely with the microbe and elemental sulfur as precursors, can effectively address these issues for stable high-capacity Na–S and K–S batteries. The covalently bonded short-chain sulfur species enable superior reaction kinetics and avoid soluble polysulfide formation. The microcage architecture with built-in cavities buffers the volume deformation to ensure a resilient electrode. The resultant conductive organosulfur polymer can promise a combination of high capacity and extraordinary cyclability with a promising rate and Coulombic efficiency. Especially, as a K–S battery cathode, it could deliver a high capacity of 1206.5 mAh g–1 together with an extraordinary cyclability (>99% capacity retention over 1100 cycles), which is much better than that of state-of-the-art sulfur cathodes. This work envisions new perspectives on building conductive organosulfur cathode materials with high performance via a simple and feasible protocol.
ISSN:0002-7863
1520-5126
1520-5126
DOI:10.1021/jacs.4c11845