Zhang Lei, Li Xiao, Tai Linlin, Shen Chunping, Yang Jun, Sun Chencheng, Geng Hongbo, Zuo Xiaobing
School of Electronic and Information Engineering, Changshu Institute of Technology, Changshu, 215500, China.
School of Material Science & Engineering, Jiangsu University of Science and Technology, Zhenjiang, 212003, China.
Nanoscale. 2021 Nov 18;13(44):18578-18585. doi: 10.1039/d1nr05521f.
Owing to their large theoretical capacity and relatively high electronic conductivity, transition metal selenides have been investigated as potential anodes for energy storage applications. On the other hand, the quick capacity decline induced by volume expansion during cycling and unconnected conducting network of the transition metal selenide-based electrode severely limit their employment in sodium-ion batteries (SIBs). Herein, a simple solvent ultrasonic technique and pyrolysis selenation process were used to make a porous N-doped carbon nanosheet-supported FeSe/CoSe electrode. The electrochemical kinetics could be improved, and the stress generated by volume expansion could be efficiently adjusted by exquisitely constructed boundary of the FeSe/CoSe-CN electrode. As expected, the FeSe/CoSe-CN porous nanosheets exhibited a high Na storage capacity of 350 mA h g (10 A g, 1000 cycles). Kinetic studies were conducted to explore the Na storage mechanism of FeSe/CoSe-CN. The as-constructed full sodium-ion batteries, when combined with NaV(PO)OF, have a phenomenal energy density (109 W h kg), encouraging the exploration of energy-related components with the high-energy density properties.
由于具有较大的理论容量和相对较高的电子导电性,过渡金属硒化物已被作为储能应用的潜在负极进行研究。另一方面,过渡金属硒化物基电极在循环过程中因体积膨胀导致的快速容量衰减以及未连接的导电网络严重限制了它们在钠离子电池(SIBs)中的应用。在此,采用简单的溶剂超声技术和热解硒化工艺制备了一种多孔氮掺杂碳纳米片负载的FeSe/CoSe电极。通过精心构建FeSe/CoSe-CN电极的边界,可以改善电化学动力学,并有效调节体积膨胀产生的应力。正如预期的那样,FeSe/CoSe-CN多孔纳米片表现出350 mA h g(10 A g,1000次循环)的高钠存储容量。进行了动力学研究以探索FeSe/CoSe-CN的钠存储机制。所构建的全钠离子电池与NaV(PO)OF组合时,具有惊人的能量密度(109 W h kg),这鼓励了对具有高能量密度特性的能量相关组件的探索。