电解质
超级电容器
电化学
化学工程
电化学窗口
材料科学
杂原子
水溶液
功率密度
比表面积
无机化学
化学
电极
离子电导率
有机化学
物理化学
功率(物理)
催化作用
工程类
物理
量子力学
戒指(化学)
作者
Xiao Wang,Kaixiang Zou,Weijing Wu,Yuanfu Deng,Guohua Chen
标识
DOI:10.1016/j.cclet.2021.11.057
摘要
Designing a carbon material with a unique composition and surface functional groups for offering high specific capacity in a wide voltage window is of great significance to improve the energy density for the supercapacitor in a cheap and eco-friendly aqueous electrolyte. Herein, we develop an efficient strategy to synthesize a N, O co-doped hierarchically porous carbon (NODPC-1.0) with moderate specific surface area and pore volume as well as rich heteroatoms using a deep eutectic solvent (DES) as an activator. It is found that NODPC-1.0 with a large proportion of pseudocapacitive functional groups (pyrrole-N, pyridine-N and carbonyl-quinone) can work stable in an acidic 2 mol/L Li2SO4 (pH 2.5) electrolyte, exhibiting specific capacities of 375 and 186 F/g at the current densities of 1.0 and 100 A/g, respectively. Also, the assembled symmetric capacitor using the NODPC-1.0 as the active material and 2 mol/L acidic Li2SO4 (pH 2.5) as the electrolyte shows an outstanding energy density of 74.4 Wh/kg at a high power density of 1.44 kW/kg under a broad voltage window (2.4 V). Relevant comparative experiments indicate that H+ of the acidic aqueous electrolyte plays a crucial part in enhancement the specific capacity, and the abundant pseudocapacitive functional groups on the surface of the NODPC-1.0 sample play the key role in the improvement of electrochemical cycle stability under a broad voltage window.
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