材料科学
阳极
锂(药物)
复合数
离子
纳米颗粒
电导率
扩散
兴奋剂
碳纤维
化学工程
纳米技术
光电子学
复合材料
电极
物理化学
化学
有机化学
医学
物理
工程类
热力学
内分泌学
作者
Zhenwei Li,Yuan Fu,Meisheng Han,Jie Yu
出处
期刊:Small
[Wiley]
日期:2022-06-07
卷期号:18 (27)
被引量:16
标识
DOI:10.1002/smll.202202495
摘要
WS2 anode materials show huge potential for fast-charging lithium-ion batteries (LIBs) due to the naturally good 2D diffusion pathways but suffer from large Li+ diffusion barrier energy and poor intrinsic electrical conductivity. Here, a defect-rich atomic-scale laminated structure of WS2 and C (D-WS2 -C) with O doping and enlarged interlayer distance from 0.62 to 1.06 nm of WS2 is first fabricated, which is assembled into micron-sized spheres to prepare WS2 /C composite microspheres. D-WS2 -C with maximized molecular layer contact area between WS2 and carbon and large interlayer spacing greatly enhances the electrical conductivity of WS2 and reduces Li-ion diffusion energy barrier, confirmed by density functional theory calculations. Besides, the unique D-WS2 -C enables the formation of vast superfine W nanoparticles (1-2 nm) during the conversation reaction, resulting in the construction of a space charge zone on W surface. Based on these characteristics of D-WS2 -C, the prepared WS2 /C composite microspheres show superior fast-charging capability with a high capacity of 647.8 mAh g-1 at 20 C in half cells. For full cells, a high-energy density of 100.9 Wh kg-1 is achieved at a charge time of only 8.5 min at 5 C, representing the best fast-charging performances in WS2 -based anode materials to date.
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