材料科学
杂原子
阳极
插层(化学)
电池(电)
兴奋剂
钾离子电池
钾
碳纤维
离子
纳米技术
化学工程
无机化学
复合数
复合材料
电极
冶金
磷酸钒锂电池
有机化学
光电子学
戒指(化学)
功率(物理)
化学
物理
物理化学
量子力学
工程类
作者
Junling Wang,Zhijiao Huang,Wei Zhang,Qinghua Li,Zhixin Liang,Jingjing Lu,Zeyu Lin,Guang Wang,Junxiong Wu,Shaoming Huang
标识
DOI:10.1002/adfm.202409937
摘要
Abstract Hard carbons (HCs) have emerged as promising candidates for commercial anodes in potassium‐ion batteries (PIBs). However, a thorny challenge remains in achieving high reversible capacities at high charge/discharge rates, which significantly hinders the development of HCs for PIBs. Here, a temperature‐controlled strategy is proposed to effectively balance graphitic nanodomains and heteroatom doping content in HCs, resulting in widened carbon layer spacing, high conductivity, and abundant K‐ion intercalation sites. The optimized NO‐HC 600 electrode exhibits a high reversible capacity of 315.0 mAh g −1 at 0.2 A g −1 , and exceptional cyclic stability (235.0 mAh g −1 after 1200 cycles at 2.0 A g −1 with a capacity retention rate of 98.82%). Furthermore, systematic in /ex situ experiments unveil a highly reversible “adsorption–intercalation” mechanism governing potassium‐ion storage, confirming the origin of the superior performance. This work offers valuable insights into the facile preparation of HC anodes with high reversible capacity and fast charge/discharge capability for PIBs.
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