插层(化学)
阳极
材料科学
石墨
碳纤维
扩散
锂(药物)
微晶
离子
化学工程
阴极
纳米技术
无机化学
复合材料
冶金
化学
有机化学
电极
热力学
复合数
物理化学
工程类
内分泌学
物理
医学
作者
Qi Li,Yibo Zhang,Zhengyu Chen,Jun Zhang,Ying Tao,Quan‐Hong Yang
标识
DOI:10.1002/aenm.202201574
摘要
Abstract Graphite has paved the way for commercial lithium‐ion batteries and shows great potential as an anode for high‐energy potassium‐ion batteries (PIBs) due to its low‐potential charge/discharge plateau. However, the restricted diffusion of large K + in graphite causes difficulties in generating the stage‐one graphite‐intercalation compound (GIC) KC 8 at high rates and results in a low plateau capacity and an inferior rate performance. It is discovered that the formation of high‐stage GICs (prior to KC 24 ) is the rate‐controlling step of K + intercalation, which is key to forming KC 8 . Here, a carbon anode material containing the medium‐size discrete graphitic crystallites is reported, produced by heating non‐graphitizable carbon above 2800 °C. This carbon anode material promotes the formation of KC 8 due to the accelerated K + diffusion especially at the rate‐controlling step and the sufficient reactive sites, which leads to a record‐high plateau capacity of 293 mAh g −1 and an excellent rate performance with 180 mAh g −1 at 500 mA g −1 . For comparison, the respective values for graphite are only 242 and 51 mAh g −1 . This study provides new insights into K + ‐intercalation chemistry and shall promote the design of carbon anode materials for high‐energy and high‐power PIBs and even other energy storage systems.
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