Deng Qixiang, Wang Mengqi, Liu Xinlong, Fan Haosen, Zhang Yufei, Yang Hui Ying
School of Chemistry and Chemical Engineering, Guangzhou University, Guangzhou 510006, China; Pillar of Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, 487372, Singapore.
School of Chemistry and Chemical Engineering, Guangzhou University, Guangzhou 510006, China.
J Colloid Interface Sci. 2022 Nov 15;626:700-709. doi: 10.1016/j.jcis.2022.06.073. Epub 2022 Jun 21.
Sodium-ion batteries (SIBs) have received increasing interest for large-scale energy storage based on the high natural abundance and low-cost of sodium resources. However, owing to the large ionic radius of sodium ion, SIBs anodes exhibit sluggish charge kinetic and rapid capacity decay, which severely hindered their practical application. In this work, we develop a novel approach to couple two-dimensional (2D) bimetal Co-Ni selenide nanosheets with TiC MXene (TiC/CoNiSe) as anode material for SIBs. Specifically, the 2D bimetal nanosheets anchoring on MXene substrate can provide high specific capacity and alleviate volume expansion. Furthermore, the MXene substrate can shorten the diffusion pathway of sodium-ion and enhance electronic conductivity. The TiC/CoNiSe delivers a superior rate performance of 337 mAh g at 3000 mA g and excellent stability of 338 mAh g at 1000 mA g after 600 cycles. The presented strategy from combination of MXene and 2D bimetallic selenide may pave a way for the design and synthesis of high-performance SIBs anode materials.
基于钠资源的高天然丰度和低成本,钠离子电池(SIBs)在大规模储能方面受到了越来越多的关注。然而,由于钠离子的离子半径较大,SIBs负极表现出缓慢的充电动力学和快速的容量衰减,这严重阻碍了它们的实际应用。在这项工作中,我们开发了一种新方法,将二维(2D)双金属Co-Ni硒化物纳米片与TiC MXene(TiC/CoNiSe)耦合作为SIBs的负极材料。具体而言,锚定在MXene基底上的二维双金属纳米片可以提供高比容量并缓解体积膨胀。此外,MXene基底可以缩短钠离子的扩散路径并提高电子导电性。TiC/CoNiSe在3000 mA g下具有337 mAh g的优异倍率性能,在1000 mA g下经过600次循环后具有338 mAh g的出色稳定性。所提出的将MXene和二维双金属硒化物相结合的策略可能为高性能SIBs负极材料的设计和合成铺平道路。