Scalable Upcycling of Industrial Waste Polytetrafluoroethylene Into Porous Carbon Nanosheets by Zeolite Particle Templates for Capacitive Energy Storage.

IF 16.9
Keyang Li, Menggang Li, Yunfeng Feng, Peng Zhang, Chenhui Zhou, Zhuangzhuang He, Yihong Liu, Mengda Hou, Jianning Gan, Rongpei Wang, Yilun Huang, Menghao Yang, Ming Zhao, Daming Zhuang, Qianming Gong, Shaojun Guo
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Abstract

Upcycling highly stable polytetrafluoroethylene (PTFE) waste into value-added carbon materials is fundamentally hindered by its complete zero-residue pyrolysis, which exclusively emits hazardous fluorocarbons rather than forming solid carbon frameworks. Herein, we present a scalable zeolite-particle-templated cocarbonization strategy that catalytically transforms industrial PTFE waste into hierarchical porous carbon nanosheets (PCNs) while fixing over 81% of the fluorine as recyclable NaF. Comprehensive mechanistic investigations reveal that the ZSM-5 template electronically activates C─F bonds and lowers the defluorination barrier, driving a successive-condensation structural evolution. The resulting PCN, featuring an ultrahigh specific surface area and hierarchical porosity, delivers exceptional dual-mode energy storage performances. In supercapacitors, PCNs achieve a remarkable specific capacitance of 429.6 F g-1 and outstanding rate capabilities driven by reversible pseudocapacitance and ion coadsorption. Concurrently, in carbon-based aqueous zinc-ion batteries (CAZBs), the PCNs deliver a high specific capacity of 267.0 mAh g-1 with robust extreme-temperature adaptability (-25°C). Validated by a continuous industrial-scale piping and instrumentation design (PID), this strategy demonstrates high commercial viability with low energy storage costs, pioneering a waste-to-wealth strategy for advanced carbon materials for energy storage.

利用沸石颗粒模板可扩展地将工业废渣聚四氟乙烯升级为多孔碳纳米片用于电容储能。
将高度稳定的聚四氟乙烯(PTFE)废弃物升级为增值碳材料,从根本上受到阻碍,因为其完全零残留热解,只会排放有害的氟碳化合物,而不会形成固体碳框架。在此,我们提出了一种可扩展的沸石颗粒模板共碳化策略,该策略催化将工业聚四氟乙烯废物转化为分层多孔碳纳米片(PCNs),同时将超过81%的氟固定为可回收的NaF。综合机理研究表明,ZSM-5模板通过电子激活C─F键,降低脱氟势垒,推动了连续缩聚结构的演化。由此产生的PCN具有超高比表面积和分层孔隙率,具有卓越的双模储能性能。在超级电容器中,PCNs的比电容达到了429.6 F -1,并且在可逆伪电容和离子共吸附的驱动下具有出色的倍率能力。同时,在碳基水性锌离子电池(cazb)中,pcn提供267.0 mAh g-1的高比容量,具有强大的极端温度适应性(-25°C)。通过连续工业规模的管道和仪表设计(PID)验证,该策略具有较高的商业可行性和较低的储能成本,开创了用于储能的先进碳材料的废物转化财富策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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