He Yi, Li Hong, Zhang Qing, He Chengen, Zhang Xiaofang, Yang Yingkui
Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education, Hubei Key Laboratory of Catalysis and Materials Science, South-Central University for Nationalities Wuhan 430074 China
Hubei Engineering Technology Research Centre of Energy Polymer Materials, School of Chemistry and Materials Science, South-Central University for Nationalities Wuhan 430074 China
RSC Adv. 2019 Dec 11;9(70):40933-40939. doi: 10.1039/c9ra06289k. eCollection 2019 Dec 9.
The combination of activity-enriched heteroatoms and highly-conductive networks is a powerful strategy to craft carbon-based electrodes for high-efficiency electrochemical energy storage. Herein, N-doped carbon (N-C) coated carbon nanotubes (N-CNTs) were fabricated a facile synthesis of polyimide in the presence of carbon nanotubes (CNTs), followed by carbonization. The polyimide-divided N-C layers were uniformly covered on the surface of CNTs with a tailored layer thickness. The as-fabricated N-CNTs were further used as electrode active materials for energy storage. When employed as the electrodes for supercapacitors, the N-CNTs exhibited a specific capacitance of 63 F g at 0.1 A g (an energy density of 1.4 W h kg at a power density of 20 W kg), which was much higher than that of pure N-C (5 F g) and CNTs (13 F g). The supercapacitor also retained 66.7% of its initial capacitance (42 F g at 10 A g) after a 100-fold increase in the current density and nearly 100% of its initial capacitance after running 10 000 cycles. Furthermore, functioning as an anode material for a Li-ion battery, the N-CNTs also delivered a larger reversible capacity (432 mA h g at 50 mA g), higher rate capability, and better cycling stability compared to pure CNTs. The electrochemical performances of the N-CNTs were improved overall due to the synergistic effects of interconnected 3D networks and core-shell structures capable of facilitating electrolyte percolation and charge transportation, enhancing conductivity and surface/interface wettability, and contributing additional pseudocapacitance.
将富含活性的杂原子与高导电网络相结合,是制备用于高效电化学储能的碳基电极的有力策略。在此,通过在碳纳米管(CNT)存在下简便合成聚酰亚胺,随后进行碳化,制备了氮掺杂碳(N-C)包覆的碳纳米管(N-CNTs)。聚酰亚胺分隔的N-C层以定制的层厚度均匀覆盖在CNT表面。所制备的N-CNTs进一步用作储能的电极活性材料。当用作超级电容器的电极时,N-CNTs在0.1 A g下表现出63 F g的比电容(在功率密度为20 W kg时能量密度为1.4 W h kg),这远高于纯N-C(5 F g)和CNT(13 F g)。在电流密度增加100倍后,超级电容器还保留了其初始电容的66.7%(在10 A g下为42 F g),在运行10000次循环后几乎保留了其初始电容的100%。此外,作为锂离子电池的负极材料,与纯CNT相比,N-CNTs还具有更大的可逆容量(在50 mA g下为432 mA h g)、更高的倍率性能和更好的循环稳定性。由于相互连接的3D网络和核壳结构的协同效应,N-CNTs的电化学性能总体上得到了改善,这些效应能够促进电解质渗透和电荷传输,提高导电性和表面/界面润湿性,并贡献额外的赝电容。