Liu Chang, Feng Xiangping, Zhao Yutong, Fan Huilin, Zheng Runguo, Wang Zhiyuan, Arandiyan Hamidreza, Wang Yuan, Bhargava Suresh K, Liu Yanguo, Sun Hongyu, Shao Zongping
School of Materials Science and Engineering, Northeastern University, Shenyang 110004, PR China.
School of Materials Science and Engineering, Northeastern University, Shenyang 110004, PR China; School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004, PR China; Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province, Northeastern University at Qinhuangdao, Qinhuangdao 066004, PR China.
J Colloid Interface Sci. 2023 Dec 15;652(Pt B):1325-1337. doi: 10.1016/j.jcis.2023.08.165. Epub 2023 Aug 26.
Mesoporous carbon spheres (MCSs) show great potential for using as high-performance anodes in potassium-ion batteries (PIBs). Design and synthesis of MCSs with suitable multiscale structures and heteroatom doping or co-doping in MCSs are successfully employed to optimize the ion and electron transportation, however, it is still a challenge to explore MCS-based anodes with satisfactory potassium storage performance. In this work, we report novel S-doped MCS samples with abundant internal surfaces for potassium storage. The S doping sites are controlled during the synthesis, and the effect of different doping sites on the potassium storage is systematically studied. It is found that S doping between the carbon layers enlarges interlayer spacing and facilitates potassium ion adsorption. Consequently, the optimized sample shows an excellent rate capability of 144 mAh/g at 5.0 A/g, and a high reversible specific capacity of 325 mAh/g after 100 cycles at 0.1 A/g with a capacity retention of 91.2%. The important role of element doping sites on ion adsorption and ion storage performance is confirmed by theoretical investigations. Controlling the doping sites in MCSs provides a new approach to designing high-performance electrodes for energy storage and conversion applications.
介孔碳球(MCSs)在用作钾离子电池(PIBs)的高性能负极方面显示出巨大潜力。设计和合成具有合适多尺度结构的MCSs以及在MCSs中进行杂原子掺杂或共掺杂已成功用于优化离子和电子传输,然而,探索具有令人满意的钾存储性能的基于MCSs的负极仍然是一个挑战。在这项工作中,我们报道了具有丰富内表面用于钾存储的新型硫掺杂MCS样品。在合成过程中控制硫掺杂位点,并系统研究了不同掺杂位点对钾存储的影响。发现碳层间的硫掺杂扩大了层间距并促进了钾离子吸附。因此,优化后的样品在5.0 A/g下表现出144 mAh/g的优异倍率性能,在0.1 A/g下循环100次后具有325 mAh/g的高可逆比容量,容量保持率为91.2%。理论研究证实了元素掺杂位点对离子吸附和离子存储性能的重要作用。控制MCSs中的掺杂位点为设计用于能量存储和转换应用的高性能电极提供了一种新方法。