Wan Lijia, Chua Daniel H C, Sun Hengchao, Chen Lei, Wang Kai, Lu Ting, Pan Likun
Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University, Shanghai 200062, China.
Department of Materials Science and Engineering, National University of Singapore 117574, Singapore.
J Colloid Interface Sci. 2021 Apr 15;588:147-156. doi: 10.1016/j.jcis.2020.12.071. Epub 2020 Dec 31.
The development of battery systems with high specific capacity and power density could fuel various energy-related applications from personal electronics to grid storage. (FeTi)O possessing high theoretical specific capacity has been considered as a promising high rate anode material for lithium ion batteries due to the replacement of Fe (0.64 Å) by Ti (0.68 Å) with a larger radius to expand the interlayer space for ion intercalation. However, its extreme volume variation upon cycling as well as poor electrical conductivity hinder its further application. To tackle the above problems, in this work, we successfully synthesized two-dimensional (2D) (FeTi)O/C/MXene architecture derived from TiCT MXene via solvo-hydrothermal, ultrasound hybridizing and high temperature annealing processes. The (FeTi)O/C/MXene shows a high discharge capacity of 757.2 mAh g after 800 cycles at a current density of 3 A g with excellent rate performance. The superior electrochemical performances are triggered primarily by the incorporation of carbon and MXene into (FeTi)O moiety to construct a 2D layered structure, which can improve the ion diffusion and electron transport. In addition, the synergistic contributions from diffusion controlled and capacitive processes for (FeTi)O/C/MXene improve the ion diffusion rate and offer high specific capacity at high current density. The MXene-derived synthesis strategy in this work should be a promising pathway to synthesize other anode materials with 2D layered architecture for high performance lithium storage.
具有高比容量和功率密度的电池系统的发展可以推动从个人电子设备到电网储能等各种与能源相关的应用。由于半径较大的Ti(0.68 Å)取代了Fe(0.64 Å)以扩大离子嵌入的层间空间,具有高理论比容量的(FeTi)O被认为是一种有前途的锂离子电池高倍率负极材料。然而,其在循环过程中的极端体积变化以及较差的导电性阻碍了它的进一步应用。为了解决上述问题,在这项工作中,我们通过溶剂热、超声混合和高温退火工艺成功合成了源自TiCT MXene的二维(2D)(FeTi)O/C/MXene结构。(FeTi)O/C/MXene在3 A g的电流密度下循环800次后显示出757.2 mAh g的高放电容量,具有优异的倍率性能。优异的电化学性能主要是由碳和MXene掺入(FeTi)O部分以构建二维层状结构触发的,这可以改善离子扩散和电子传输。此外,(FeTi)O/C/MXene的扩散控制和电容过程的协同作用提高了离子扩散速率,并在高电流密度下提供高比容量。这项工作中源自MXene的合成策略应该是合成其他具有二维层状结构的负极材料以实现高性能锂存储的一条有前途的途径。