材料科学
化学工程
离子
超短脉冲
锂(药物)
钠
碳纤维
纳米技术
光学
复合材料
复合数
有机化学
冶金
激光器
内分泌学
工程类
化学
物理
医学
作者
Peng Zhang,Razium Ali Soomro,Zhaoruxin Guan,Ning Sun,Bin Xu
标识
DOI:10.1016/j.ensm.2020.04.016
摘要
MXenes have recently emerged as a promising candidate for energy storage devices due to their high volumetric capacitance and robust energy profile. However, MXenes are prone to surface oxidation and layer re-stacking, which compromise their practical applications in energy storage. Here, we propose a simple approach to directly transform 2D T3C2Tx MXene nanosheets into 3D carbon-coated T3C2Tx architecture. The nanohybrid was synthesized by achieving self-polymerization of dopamine over the surface of pristine Ti3C2Tx nanosheets followed by freeze-drying and carbonization under an inert air atmosphere. The self-polymerization of dopamine not only facilitated the transformation of 2D Ti3C2Tx sheets into 3D tremella-like architecture, but its subsequent carbonization resulted in complete coverage of a thin carbon coating that preserves the structure from both air-oxidation and structural aggregation. The 3D tremella-like architecture ([email protected]) with active and stable surface-facets facilitated fast charge transportation, ultrahigh capacity, superior rate performance, and long cyclability when being used as anode material for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). In the case of LIBs, the [email protected] exhibited a high capacity of 499.4 mA h g−1 at 0.2 C and 101.5 mA h g−1 at 100 C. Whereas, a high capacity of 257.6 mA h g−1 at 0.05 A g−1 after 200 cycles and 77.8 mA h g−1 at 10 A g−1 were obtained for SIBs, respectively. In addition, long cycle durability with a capacity retention of 91.7% at 1 A g−1 after 3000 cycles with a 0.00277% decay per cycle was achieved, endowing [email protected] capability to serve as a prospective hybrid for the energy applications.
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