材料科学
阴极
多孔性
碳纤维
化学工程
聚乙烯
电化学
水溶液
苯
比表面积
电流密度
阳极
复合材料
纳米技术
法拉第效率
碳纳米管
聚合物
储能
多孔介质
废物管理
电池(电)
化学稳定性
容量损失
离子
作者
Hao-Rui Shu,Jiali Gao,Run Wang,Hai-Yun Zhou,Yang-Yi Yang,Bao-Hui Ye,G. Liu
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2026-01-06
卷期号:40 (2): 1416-1430
标识
DOI:10.1021/acs.energyfuels.5c05067
摘要
Waste plastics persist in the environment and threaten ecosystems, yet their high carbon content offers an opportunity for value-added upcycling. Here, three representative waste plastics, high-density polyethylene (HDPE), poly(vinyl chloride) (PVC), and poly(ethylene terephthalate) (PET)–are upcycled into hierarchical porous carbons via one-step carbonization-activation, and their performances as cathodes for aqueous zinc–iodine (Zn–I2) batteries are benchmarked. Results indicate that PET-derived porous carbon (PET–PC) exhibits the highest specific surface area, abundant hierarchical pore structure, and excellent graphitization due to its rigid benzene ring structure and ester group self-activation. This significantly enhances iodine immobilization capacity and ion transport kinetics. Electrochemical testing revealed that the PET–PC cathode maintained a specific capacity of 125.5 mAh g–1 and a capacity retention rate of 88.1% after 2000 cycles at a current density of 5 A g–1, demonstrating outstanding cycling stability and rate performance. This study provides a strategy for the high-value utilization of waste plastics and offers theoretical foundations and practical references for cathode material design in zinc–iodine batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI