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Facile fabrication of N-doped hierarchical porous carbon@CNT coaxial nanocables with high performance for energy storage and conversion

机译:方便地制造具有高性能的N掺杂多层多孔碳@CNT同轴纳米电缆,用于能量存储和转换

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Developing a facile and cost-effective design and fabrication method to realize an optimal carbon nanoarchitecture containing hierarchical pores, appropriate N doping and high conductivity for high-performance in energy storage and conversion is still a challenge. Herein, we have facilely achieved an intriguing heterostructure of N-doped hierarchical porous carbon@CNT coaxial nanocables (HPNCNTs) via a one-step carbonization of resorcinol-melamine-formaldehyde resin (RMF)@CNT shell@core nanostructures. Significantly, we have demonstrated that the RMF@CNT shell@core nanostructures, with their inherent microporous structure and proper N-containing functionalities, represent the ideal precursor for realizing carbon heterostructures for electrochemical performance optimization for supercapacitors and in the oxygen reduction reaction (ORR). The results show that the HPNCNTs exhibit a specific capacitance of 284 F g(-1), much higher than that of CNTs and most of the reported N-doped carbons, a good rate capability and a robust cycling performance with no capacity fading even after 6000 cycles. Furthermore, HPNCNTs show high electrocatalytic activity for the ORR with an onset potential of -0.04 V (vs. Ag/AgCl), a dominant four-electron pathway (n = 3.84), long-term stability, and excellent resistance to crossover effects superior to that of the commercial Pt/C. The present investigation opens the avenue for creating carbon heterostructures with a desirable porous tissue and morphology through a facile and general route for future high-performance renewable energy storage and conversion devices.
机译:开发一种简便且具有成本效益的设计和制造方法,以实现一种最佳的碳纳米结构,该碳纳米结构包含分层的孔,适当的N掺杂和高电导率以在能量存储和转换方面实现高性能仍然是一个挑战。在本文中,我们通过间苯二酚-三聚氰胺-甲醛树脂(RMF)@CNT壳@核纳米结构的一步碳化,轻松实现了N掺杂的多层多孔碳@CNT同轴纳米电缆(HPNCNT)的有趣异质结构。重要的是,我们已经证明,RMF @ CNT壳@核纳米结构具有固有的微孔结构和适当的含N官能度,是实现碳异质结构的理想前体,以实现超级电容器的电化学性能优化和氧还原反应(ORR) 。结果表明,HPNCNTs的比电容为284 F g(-1),远高于CNT和大多数报道的N掺杂碳的比电容,具有良好的速率能力和鲁棒的循环性能,即使在使用后也不会褪色6000次循环。此外,HPNCNT对ORR表现出高电催化活性,起始电位为-0.04 V(vs. Ag / AgCl),占主导地位的四电子通路(n = 3.84),长期稳定,并且具有优异的抗交叉作用性能到商业Pt / C。本研究为将来的高性能可再生能源存储和转换设备提供了一条简便而通用的途径,以创建具有理想的多孔组织和形态的碳异质结构。

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