Ultra-stable potassium storage and hybrid mechanism of perovskite fluoride KFeF/rGO

Potassium-ion batteries (PIBs) are promising for large-scale energy storage due to the abundant reserves of the element potassium yet few satisfactory cathode materials have been developed due to the limitation of the large ionic radius of the potassium ion. Cubic perovskite fluorides have three-dim...

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Published inNanoscale Vol. 14; no. 14; pp. 5347 - 5355
Main Authors Wang, Shuo, Chen, Fei, Zhang, Li-ming, Li, Yi-xuan, Ren, Nai-qing, Cao, Kuo, Xiao, Jing-chao, Chen, Chun-hua
Format Journal Article
Published 07.04.2022
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Summary:Potassium-ion batteries (PIBs) are promising for large-scale energy storage due to the abundant reserves of the element potassium yet few satisfactory cathode materials have been developed due to the limitation of the large ionic radius of the potassium ion. Cubic perovskite fluorides have three-dimensional diffusion channels and a robust structure, which are favorable for ion transfer, but their poor electronic conductivity needs to be compensated. Here, we synthesized cubic KFeF 3 powder by a solvothermal procedure. After the combination with reduced graphene oxide (rGO) and carbon coating, its electronic conductivity is greatly improved. In the optimal sample KFeF 3 /rGO-PVA-500, KFeF 3 nano-particles (smaller than 50 nm) distribute on the rGO surface evenly. Owing to the special structure, KFeF 3 /rGO-PVA-500 provides an excellent rate performance and cycling stability. In particular, a high capacity retention of 94% is obtained after 1000 cycles at 200 mA g −1 . In addition, a hybrid reaction mechanism combining mainly solid solution and partly conversion processes is revealed by employing in situ and ex situ characterization. Combining rGO composite and carbon coating strategies, the nano-KFeF 3 presents excellent rate property and ultra-stable cycle performance. The reaction mechanism of nano-KFeF 3 consists of mainly solid solution and partly conversion processes.
Bibliography:https://doi.org/10.1039/d2nr00493c
Electronic supplementary information (ESI) available. See DOI
ISSN:2040-3364
2040-3372
DOI:10.1039/d2nr00493c