材料科学
硫黄
化学工程
兴奋剂
电容器
溶剂
离子
钠
碳纤维
基质(化学分析)
无机化学
纳米技术
有机化学
电压
化学
复合材料
冶金
光电子学
复合数
量子力学
物理
工程类
作者
Hongyu Zhang,Baolin Liu,Zhenjiang Lu,Jindou Hu,Jing Xie,Aize Hao,Yali Cao
出处
期刊:Small
[Wiley]
日期:2023-01-20
卷期号:19 (16)
被引量:38
标识
DOI:10.1002/smll.202207214
摘要
The exploitation of electrode materials with ability to balance capacity and kinetics between cathode and anode is a challenge for sodium-ion hybrid capacitors (SIHCs). Mn-based anode materials are limited by poor electrical conductivity, sluggish reaction kinetics, large volume variation, weak cycling stability, and inferior reversible capacity. Herein, MnS nanocubes encapsulated in S-doped porous carbon matrix (MSC) with strong sulfur-bridged bond interactions (CSMn) are successfully synthesized by solvent-free tactics. The CSMn bonds generated between MnS and carbon significantly inhibit the aggregation of nanostructural MnS cubes, restrict the volume expansion, and stabilize the nanostructure, which improves the Na+ storage reversibility and stability. Moreover, S-doped porous carbon enhances the electrical conductivity and electrons/ions diffusion rate, which boosts a fast kinetic reaction. As expected, MSC anode presents an outstanding reversible capacity of 600 mAh g-1 at 0.2 A g-1 and a long-term stable capacity of 357 mAh g-1 for 1000 cycles at a high current density of 10 A g-1 in sodium-ion batteries (SIBs). The as-assembled SIHCs deliver a high energy density of 109 W h kg-1 and a high power output of 98 W kg-1 , with 88% capacity retention at 2 A g-1 after 2000 cycles and practical applications (55 LEDs can be lighted for 10 min).
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