二硫化钼
电化学
材料科学
动力学
化学工程
电化学动力学
碳纤维
电极
氮气
兴奋剂
扩散
纳米技术
化学
复合数
物理化学
复合材料
光电子学
有机化学
工程类
物理
热力学
量子力学
作者
Jiabao Li,Shaocong Tang,Ziqian Li,Chengyin Wang,Jinliang Li,Xiaodan Li,Zibiao Ding,Likun Pan
出处
期刊:Chemsuschem
[Wiley]
日期:2021-10-27
卷期号:14 (23): 5293-5303
被引量:28
标识
DOI:10.1002/cssc.202101902
摘要
Although it is a promising sodium storage material due to its excellent electrochemical activity, small bandgap, and large interlayer spacing, layered molybdenum disulfide (MoS2 ) suffers from poor rate capability and degraded cycling life, resulting from its serious aggregation upon preparation, sluggish reaction kinetics, and structure expansion during cycling. To address these issues, a polyethyleneimine (PEI)-assisted fabrication approach was developed for the rational synthesis of an interconnected framework with nitrogen-doped carbon-confined MoS2 nanosheets/Ti3 C2 Tx MXene (MoS2 /Ti3 C2 Tx @NC), where the PEI could guide the uniform growth of MoS2 on Ti3 C2 Tx and the self-generated NC simultaneously enhanced its synergistic coupling with MoS2 /Ti3 C2 Tx , thus contributing to the improvement of charge transfer, diffusion kinetics, and structural integrity of the hybrid electrode. Consequently, the desired MoS2 /Ti3 C2 Tx @NC delivered impressive sodium storage performance, demonstrating high reversible capacities of 397.3 and 206.8 mAh g-1 at 0.1 A g-1 after 100 cycles and 0.5 A g-1 after 500 cycles, respectively. Moreover, electrochemical kinetics analysis and charge storage mechanism manifested that high capacitive contribution, facilitated Na+ transport pathways, and synergistic electronic coupling between MoS2 /Ti3 C2 Tx and NC contributed to the superior sodium storage performance.
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