阳极
对偶(语法数字)
生物量(生态学)
碳纤维
离子
环境科学
材料科学
工艺工程
化学
工程类
电极
复合材料
地质学
海洋学
复合数
文学类
艺术
物理化学
有机化学
作者
Rui Zhou,Rui Liu,Yun‐Nuo Li,Si‐Jie Jiang,Tian-Tian Jing,Yan‐Song Xu,Feifei Cao
出处
期刊:
日期:2025-08-28
卷期号:31 (8)
被引量:8
标识
DOI:10.61558/2993-074x.3569
摘要
Dual-ion batteries (DIBs) usually use carbon-based materials as electrodes, showing advantages in high operating voltage, potential low cost, and environmental friendliness. Different from conventional “rocking chair” type secondary batteries, DIBs perform a unique working mechanism, which employ both cation and anion taking part in capacity contribution at an anode and a cathode, respectively, during electrochemical reactions. Graphite has been identified as a suitable cathode material for anion intercalation at high voltages (> 4.8 V) with fast reaction kinetics. However, the development of DIBs is being hindered by dynamic mismatch between a cathode and an anode due to sluggish Li+ diffusion at a high rate. Herein, we prepared phyllostachys edulis derived carbon (PEC) through microstructure regulation strategy and investigated the carbonized temperature effect, which effectively tailored the rich short-range ordered graphite microdomains and disordered amorphous regions, as well as a unique nano-pore hierarchical structure. The pore size distribution of nano-pores was concentrated in 0.5–5 nm, providing suitable channels for rapid Li+ transportation. It was found that PEC-500 (carbonized at 500 °C) achieved a high capacity of 436 mAh·g–1 at 300 mA·g–1 and excellent rate performance (maintaining a high capacity of 231 mAh·g–1 at 3 A·g–1). The assembled dual-carbon PEC-500||graphite full battery delivered 114 mAh·g–1 at 10 C with 96% capacity retention after 3000 cycles and outstanding rate capability, providing 74 mAh·g–1 at 50 C.
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