材料科学
阳极
锂(药物)
纳米颗粒
化学工程
碳纳米纤维
介孔材料
电化学
静电纺丝
碳纤维
储能
纳米纤维
纳米技术
电极
碳纳米管
复合材料
复合数
化学
催化作用
聚合物
内分泌学
工程类
物理化学
生物化学
功率(物理)
物理
量子力学
医学
作者
Dienguila Kionga Denis,Guangyuan Wang,Linrui Hou,Guozhu Chen,Changzhou Yuan
标识
DOI:10.1016/j.electacta.2021.139564
摘要
Transition metal oxides as promising electrode materials have been widely explored for lithium-ion batteries (LIBs). Nonetheless, their practical applications are still hindered by their modest electronic conductivities, poor rate properties, and huge volume changes/rapid capacity degradation over the ceaseless delithiation/lithiation processes. To address the issues, we firstly encapsulate nano-dimensional Ni0.5Co0.5MoO4 with a solid solution structure in the carbon nanofibers (denoted as [email protected]) via a simple electrospinning technique. The uniform distribution of self-confined conductive NCMO-SS nanoparticles (NPs) with a high loading of ∼54.5 wt.% in the elastic CNFs framework effectively buffers the mechanical stress/volume change, reinforces the structural integrity, and brings abundant active phase boundaries, favoring their enhanced lithium-storage properties. It is the synergistic component/composition and structure merits that make the as-obtained mesoporous [email protected] exhibit larger reversible capacities and better electrochemical stability for efficient lithium storage particularly at high rates, compared to the simple Ni/Co-molybdates and even their physical mixture. Moreover, the [email protected] full LIBs provide an energy density of ∼225.4 Wh kg‒1 and good cyclic stability. The contribution here promises a huge potential of our constructed carbon-matrix-confined NCMO-SS NPs for advanced LIBs and beyond.
科研通智能强力驱动
Strongly Powered by AbleSci AI