N-Doped Porous Carbon Cubes Exhibit Excellent Low-Temperature Performance in Symmetric Li-Ion Capacitors

重量分析 阳极 扩散 材料科学 碳纤维 兴奋剂 相(物质) 阴极 化学工程 分析化学(期刊) 吸附 多孔性 活化能 离子 电化学 锂(药物) 电极 化学 色谱法 热力学 复合材料 物理化学 有机化学 光电子学 物理 工程类 内分泌学 复合数 医学
作者
Zhihua Xiao,Zechen Li,Yankun Sun,Fangzhi Zheng,Tangyuan Pan,Dong Sun,Kai Zhao,Ziang Wang,Chunming Xu
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:12 (33): 12468-12481 被引量:2
标识
DOI:10.1021/acssuschemeng.4c03488
摘要

Fabricating high gravimetric/volumetric energy power densities along with ultralong cycle performance of carbon-based lithium-ion capacitors (LICs) in a low-temperature environment is still a huge challenge due to the sluggish Li+ diffusion rate and intrinsic unmatched kinetics between the anode and cathode. Herein, a N-doped porous carbon cube (NPCC) has been obtained through combining a facile hydrothermal and N-doping method. The NPCC owing to its unique cubic morphology, abundant hierarchical pore structures, large interlayer spacing, and high N-doped content is capable of improving the solid-phase diffusion rate of Li+, thereby improving the low-temperature performance of LICs. As a result, the as-assembled symmetric LIC of NPCC//NPCC shows the maximum gravimetric and volumetric energy densities (216.3 W h/kg and 147.8 W h/L, respectively) as well as 93.3% capacity retention ratio for 10,000 cycles at 25 °C. At a lower temperature of −30 °C, NPCC//NPCC still exhibits high capacities of 180.3 and 88.7 F/g at 1 and 10 A/g, respectively. Additionally, the symmetric LIC exhibits high gravimetric and volumetric energy densities (181.9 W h/kg and 124.2 W h/L, respectively) accompanied by 88.4% capacity retention for 10,000 cycles. To further verify the resulting outstanding electrochemical performance, the molecular dynamics simulation) models in which various N-doped atoms adsorb Li+ and PF6– have been rationally constructed. The results demonstrate that various N-doped types have a strong binding energy with Li+ and PF6–, thereby improving the solid-phase diffusion kinetics of Li+. This study will provide strong guidance for applying the porous carbon materials to low-temperature energy storage devices.
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