Yan Zhanheng, Liu Jiandong, Wei Huan, Yang Xinxin, Yao Yong, Huang Zhongyuan, Li Huanxin, Kuang Yafei, Ma Jianmin, Zhou Haihui
State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082, China.
School of Physics and Electronics, Hunan University, Changsha, Hunan 410082, China.
J Colloid Interface Sci. 2021 Jul;593:408-416. doi: 10.1016/j.jcis.2021.03.015. Epub 2021 Mar 10.
Potassium-ion batteries (PIBs) is one of the most promising alternatives for Lithium-ion batteries (LIBs) due to the low-cost and abundant potassium reserves. However, the electrochemical performances of PIBs were seriously hindered by the larger radius of potassium ions, resulting in a slow kinetic during the electrochemical reaction, especially in the PIB anodes. In the study, we propose FeS nanodots embedded S-doped porous carbon (FeS@SPC) synthesized by a simple self-template method for the storage of potassium-ions. The FeS nanodots with an average diameter of 5 nm are uniformly distributed in S-doped porous carbon nanosheets. When the FeS@SPC was used as the anode in PIBs, the unique structure of FeS@SPC can relieve the agglomeration and volume expansion of FeS effectively during the charge-discharge process. Even after 3000 cycles, the FeS nanodots are still uniformly embedded in porous carbon without agglomeration. Ascribed to the merits, the FeS@SPC exhibits a reversible capacity of 309 mAh g at 0.1 A g after 100 cycles and 232 mAh g at 1 A g after 3000 cycles. The excellent electrochemical performance of FeS@SPC is attributed to the synergistic effects of FeS nanodots and S-doped porous carbon, which facilitated the diffusion of electrolyte and accelerated the migration of potassium ions. Moreover, theoretical calculation results also suggest that the van der waals heterostructure of FeS@SPC displays higher adsorption energy for potassium ions than that of S-doped graphene, indicating the suitability of FeS@SPC for K storage.
钾离子电池(PIBs)因其低成本和丰富的钾储备,是锂离子电池(LIBs)最有前景的替代方案之一。然而,钾离子半径较大严重阻碍了PIBs的电化学性能,导致电化学反应动力学缓慢,尤其是在PIB负极中。在本研究中,我们提出了一种通过简单的自模板法合成的嵌入硫掺杂多孔碳的硫化亚铁纳米点(FeS@SPC)用于钾离子存储。平均直径为5纳米的FeS纳米点均匀分布在硫掺杂的多孔碳纳米片中。当FeS@SPC用作PIBs的负极时,其独特结构能够在充放电过程中有效缓解FeS的团聚和体积膨胀。即使经过3000次循环后,FeS纳米点仍均匀地嵌入多孔碳中而无团聚现象。得益于这些优点,FeS@SPC在100次循环后,在0.1 A g电流密度下表现出309 mAh g的可逆容量,在3000次循环后,在1 A g电流密度下表现出232 mAh g的可逆容量。FeS@SPC优异的电化学性能归因于FeS纳米点和硫掺杂多孔碳的协同效应,这促进了电解质的扩散并加速了钾离子的迁移。此外,理论计算结果还表明,FeS@SPC的范德华异质结构对钾离子的吸附能高于硫掺杂石墨烯,表明FeS@SPC适用于钾存储。