法拉第效率
热解
材料科学
阳极
碳纤维
聚对苯二甲酸乙二醇酯
钠
储能
碳化作用
化学工程
复合材料
化学
冶金
电极
工程类
复合数
物理
物理化学
功率(物理)
量子力学
作者
Dequan Chen,Kangying Luo,Zhiwei Yang,Yanjun Zhong,Zhenguo Wu,Yang Song,Guang Chen,Gongke Wang,Benhe Zhong,Xiaodong Guo
出处
期刊:Carbon
[Elsevier]
日期:2021-03-01
卷期号:173: 253-261
被引量:30
标识
DOI:10.1016/j.carbon.2020.11.004
摘要
Disordered hard carbon (HC) has shown potential as the most promising anode materials for sodium-ion batteries (SIBs). Pyrolyzing waste plastics is a sustainable alternative to obtain HC. However, most plastics will completely decompose without carbon residue or transform into highly graphitic carbon during the carbonation process because of lacking oxygen functional groups. Hence, ester bond-rich waste engineering plastics, polycarbonate (PC), and polyethylene terephthalate (PET) were selected and directly converted into HC by a simple pyrolysis method. The PC and PET-derived carbon anodes (PC-HC and PET-HC) exhibit high reversible capacities of 327 and 342 mAh·g−1 at 20 mA·g−1with remarkable initial coulombic efficiency (ICE) of 84.7% and 86.1%, respectively. Particularly, the carbon samples have no severe capacities decay after 140 cycles at 100 mA g−1. This work provides a cost-effective, easily large-scale, and eco-friendly route to fabricate HC anodes for grid-scale energy storage.
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