Xu Yang, Sun Xinpeng, Li Zhiqiang, Wei Lingzhi, Yao Ge, Niu Heling, Yang Yang, Zheng Fangcai, Chen Qianwang
Institutes of Physical Science and Information Technology, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Anhui University, Hefei, 230601, China.
Anhui Graphene Engineering Laboratory, Anhui University, Hefei, 230601, China.
Nanoscale. 2021 Dec 2;13(46):19634-19641. doi: 10.1039/d1nr06665j.
Although carbon materials have great potential for potassium ion battery (KIB) anodes due to their structural stability and abundant carbon-containing resources, the limited K-intercalated capacity impedes their extensive applications in energy storage devices. Current research studies focus on improving the surface-induced capacitive behavior to boost the potassium storage capacity of carbon materials. Herein, we designed edge-nitrogen (pyridinic-N and pyrrolic-N) doped carbon spheres with a hierarchically porous structure to achieve high potassium storage properties. The electrochemical tests confirmed that the edge-nitrogen induced active sites were conducive for the adsorption of K, and the hierarchical porous structure promoted the generation of stable solid electrolyte interphase (SEI) films, both of which endow the resulting materials with a high reversible capacity of 381.7 mA h g at 0.1 A g over 200 cycles and an excellent rate capability of 178.2 mA h g at 5 A g. Even at 5 A g, the long-term cycling stability of 5000 cycles was achieved with a reversible capacity of 190.1 mA h g. This work contributes to deeply understand the role of the synergistic effect of edge-nitrogen induced active sites and the hierarchical porous structure in the potassium storage performances of carbon materials.
尽管碳材料因其结构稳定性和丰富的含碳资源在钾离子电池(KIB)阳极方面具有巨大潜力,但有限的钾嵌入容量阻碍了它们在储能设备中的广泛应用。当前的研究集中在改善表面诱导电容行为以提高碳材料的钾存储容量。在此,我们设计了具有分级多孔结构的边缘氮(吡啶氮和吡咯氮)掺杂碳球,以实现高钾存储性能。电化学测试证实,边缘氮诱导的活性位点有利于钾的吸附,分级多孔结构促进了稳定的固体电解质界面(SEI)膜的生成,这两者都赋予所得材料在0.1 A g下200次循环中381.7 mA h g的高可逆容量以及在5 A g下178.2 mA h g的优异倍率性能。即使在5 A g下,也实现了5000次循环的长期循环稳定性,可逆容量为190.1 mA h g。这项工作有助于深入理解边缘氮诱导的活性位点与分级多孔结构的协同效应在碳材料钾存储性能中的作用。