Li Deping, Sun Qing, Zhang Yamin, Chen Lina, Wang Zhongpu, Liang Zhen, Si Pengchao, Ci Lijie
SDU & Rice Joint Center for Carbon Nanomaterials, Key Laboratory for Liquid-Solid Structural Evolution & Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, 250061, PR China.
Department of Physics, Changji College, Changji, 831100, Xinjiang, PR China.
ChemSusChem. 2019 Jun 21;12(12):2689-2700. doi: 10.1002/cssc.201900719. Epub 2019 May 15.
Potassium- (PIBs) and sodium-ion batteries (SIBs) are emerging as promising alternatives to lithium-ion batteries owing to the low cost and abundance of K and Na resources. However, the large radius of K and Na lead to sluggish kinetics and relatively large volume variations. Herein, a surface-confined strategy is developed to restrain SnS in self-generated hierarchically porous carbon networks with an in situ reduced graphene oxide (rGO) shell (SnS @C@rGO). The as-prepared SnS @C@rGO electrode delivers high reversible capacity (721.9 mAh g at 0.05 A g ) and superior rate capability (397.4 mAh g at 2.0 A g ) as the anode material of SIB. Furthermore, a reversible capacity of 499.4 mAh g (0.05 A g ) and a cycling stability with 298.1 mAh g after 500 cycles at a current density of 0.5 A g were achieved in PIBs, surpassing most of the reported non-carbonaceous anode materials. Additionally, the electrochemical reactions between SnS and K were investigated and elucidated.
钾离子电池(PIBs)和钠离子电池(SIBs)由于钾和钠资源成本低且储量丰富,正成为锂离子电池有前景的替代方案。然而,钾和钠的半径较大导致动力学缓慢且体积变化相对较大。在此,开发了一种表面限制策略,以在具有原位还原氧化石墨烯(rGO)壳的自生分级多孔碳网络中限制硫化锡(SnS @C@rGO)。所制备的SnS @C@rGO电极作为SIB的负极材料具有高可逆容量(在0.05 A g时为721.9 mAh g)和优异的倍率性能(在2.0 A g时为397.4 mAh g)。此外,在PIBs中实现了499.4 mAh g(0.05 A g)的可逆容量以及在0.5 A g电流密度下500次循环后298.1 mAh g的循环稳定性,超过了大多数已报道的非碳负极材料。此外,还对SnS与钾之间的电化学反应进行了研究和阐释。