钾
材料科学
拉曼光谱
电解质
氧化还原
锂(药物)
电池(电)
钾离子电池
无机化学
化学工程
电极
化学
磷酸钒锂电池
物理化学
工程类
内分泌学
功率(物理)
物理
冶金
光学
医学
量子力学
作者
Ke Lu,Hong Zhang,Fangliang Ye,Wei Luo,Houyi Ma,Yunhui Huang
标识
DOI:10.1016/j.ensm.2018.04.018
摘要
Potassium-ion batteries (KIBs) have emerged as attractive alternatives to dominative lithium-ion batteries for grid-level electricity storage due to lower potential of K+/K redox couple in non-aqueous electrolyte and abundant potassium resource. The current intercalation cathodes used in KIBs provide limited active sites in their frameworks while conversion chemistry offers the feasibility for much improved potassium-ion storage capability. We for the first time demonstrate a rechargeable potassium-iodine (K-I2) battery enabled by a two-electron K-I2 conversion reaction. With the help of in-situ Raman and ex-situ X-ray photoelectron spectroscopy, we confirm that the highly reversible conversion among I2, KI3 and KI involves solid-liquid-solid phase transitions and the formation of soluble KI3 intermediate enables the fast reaction kinetics. The K-I2 battery delivers a reversible capacity of 156 mA h/g and a small capacity decay of 0.058% per cycle over 500 cycles.
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