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All-Climate Aluminum-Ion Batteries Based on Binder-Free MOF-Derived FeS(2)@C/CNT Cathode
Aluminum-ion batteries (AIBs) are promising next-generation batteries systems because of their features of low cost and abundant aluminum resource. However, the inferior rate capacity and poor all-climate performance, especially the decayed capacity under low temperature, are still critical challeng...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302704/ https://www.ncbi.nlm.nih.gov/pubmed/34297240 http://dx.doi.org/10.1007/s40820-021-00682-8 |
Sumario: | Aluminum-ion batteries (AIBs) are promising next-generation batteries systems because of their features of low cost and abundant aluminum resource. However, the inferior rate capacity and poor all-climate performance, especially the decayed capacity under low temperature, are still critical challenges toward high-specific-capacity AIBs. Herein, we report a binder-free and freestanding metal–organic framework-derived FeS(2)@C/carbon nanotube (FeS(2)@C/CNT) as a novel all-climate cathode in AIBs working under a wide temperature window between −25 and 50 °C with exceptional flexibility. The resultant cathode not only drastically suppresses the side reaction and volumetric expansion with high capacity and long-term stability but also greatly enhances the kinetic process in AIBs with remarkable rate capacity (above 151 mAh g(−1) at 2 A g(−1)) at room temperature. More importantly, to break the bottleneck of the inherently low capacity in graphitic material-based all-climate AIBs, the new hierarchical conductive composite FeS(2)@C/CNT highly promotes the all-climate performance and delivers as high as 117 mAh g(−1) capacity even under −25 °C. The well-designed metal sulfide electrode with remarkable performance paves a new way toward all-climate and flexible AIBs. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-021-00682-8. |
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