沸石咪唑盐骨架
十二面体
材料科学
阴极
超级电容器
化学工程
咪唑酯
水溶液
储能
兴奋剂
多孔性
纳米技术
碳纤维
电容
吸附
电极
化学
光电子学
金属有机骨架
复合材料
复合数
有机化学
工程类
物理化学
结晶学
功率(物理)
量子力学
物理
作者
Ying Yang,Deli Chen,Haiyan Wang,Pengcheng Ye,Zhentao Ping,Jiqiang Ning,Yijun Zhong,Yong Hu
标识
DOI:10.1016/j.cej.2021.133250
摘要
Aqueous Zn-ion hybrid supercapacitors (ZHSCs) are promising energy storage devices for their intrinsic advantages of high theoretical capacity, low-cost, and intrinsic safety. However, due to the lack of efficient cathode materials for reversible insertion/extraction of Zn2+ ions, it remains a pivotal challenge to high cycling-stability ZHSCs. Herein, we report a facile two-step doping strategy to synthesize zeolitic imidazolate framework (ZIF)-derived N, S-codoped porous carbon dodecahedra (N, S-PCD), using as the high-performance cathode for ultralong-life aqueous ZHSC. Integrating the hierarchical porous architecture and N, S dual-doping, the as-assembled Zn//N, S-PCD ZHSC delivers a specific capacity of 133.4 mA h g−1 (300.2 F g−1) at 0.2 A g−1, and maximum energy density of 106.7 W h kg−1 at the power density of 160 W kg−1. Moreover, an ultra-long cycle life has been achieved with the device, retaining 97.1% capacity after 100,000 charge–discharge cycles (∼3960 h), which is the maximum life span for ZHSCs to date. Mechanism studies reveal that thes dual-doping of N and S could effectively boost the chemical adsorption of Zn2+ ions and improve the electronic conductivity, which synergistically enhance the Zn-ion storage performance.
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