杂原子
碳化
材料科学
超级电容器
水溶液
化学工程
纳米技术
储能
碳纤维
多孔性
介孔材料
阴极
电化学
有机化学
电极
催化作用
扫描电子显微镜
化学
复合材料
戒指(化学)
功率(物理)
物理
物理化学
量子力学
复合数
工程类
作者
Mingquan Liu,Feng Wu,Xin Feng,Yahui Wang,Lumin Zheng,Xin Li,Ying Li,Yuteng Gong,Ying Bai,Chuan Wu
标识
DOI:10.1007/s40843-022-2176-6
摘要
Aqueous Zn-ion hybrid supercapacitors (ZHSCs) hold great potential as next-generation energy storage devices due to their low cost, excellent rate capability, long cycling life, and high safety. Heteroatom-doped hierarchical porous carbons (HD-HPCs) with integrated high specific surface area, multiscale pores, and abundant defects have been regarded as promising cathode materials for ZHSCs. However, the in situ architecture of HD-HPCs with these multiple advantages via a sustainable and controllable method remains an arduous challenge. Herein, a novel molecular engineering strategy was proposed for the in situ construction of N/P/O-doped HD-HPCs via the direct carbonization of multiple-heteroatom-rich hypermolecules. Such a strategy has multiple advantages, including the exclusion of pore-making techniques, activation agents, templates, and complicated and hazard washing processes, demonstrating its green and sustainable properties. The highly active multiple-heteroatom-rich hypermolecular precursors contributed to the formation of abundant micro/mesopores due to the self-abscission of heteroatoms and heteroatom-contiguous carbon atoms at high carbonization temperatures. Consequently, these active structural/compositional features endowed the optimal cathodes with outstanding storage capacities of 139.2 and 88.9 mA h g−1 at 0.5 and 20 A g−1 for aqueous ZHSCs, respectively. They also delivered a superior storage performance in quasi-solid ZHSCs (QS-ZHSCs) with a high specific capacity of 111.5 mA h g−1 at 0.5 A g−1. Superior energy/power densities and long cycling stability were also achieved for aqueous and QS-ZHSCs. The theoretical calculation confirmed the synergetic effects of multiple-atom doping on enhancing the electronic conductivity and reducing the energy barrier between Zn ions and carbon, which promote the Zn-ion adsorption capability. These findings shed fresh light on the straightforward manufacture of superior HD-HPCs for electrochemical energy storage.
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