阳极
材料科学
电解质
插层(化学)
阴极
电极
纳米结构
储能
化学工程
离子
纳米技术
钠
钠离子电池
扩散
无机化学
化学
冶金
物理
工程类
法拉第效率
热力学
物理化学
功率(物理)
有机化学
量子力学
作者
Cheng Chao Li,Bo Wang,Dong Chen,Li‐Yong Gan,Yuezhan Feng,Yufei Zhang,Yang Yang,Hongbo Geng,Xianhong Rui,Yan Yu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-12-17
卷期号:14 (1): 531-540
被引量:76
标识
DOI:10.1021/acsnano.9b06855
摘要
Currently, development of metal sulfide anodes for sodium-ion batteries (SIBs) with high capacity, fast charging/discharging, and good cycling performance continues to present a great challenge. Hence, a topochemical conversion strategy is reported to fabricate 2D ultrathin GeS2 nanosheets (thickness: ∼1.2 nm) as the potential anodes for sodium storage. The 2D ultrathin nanostructure can mitigate the electrode–electrolyte contact issue faced by bulk material and provide shorter transport/diffusion pathways for Na ions and electrons, resulting in excellent rate performance. Impressively, ultrathin GeS2 nanosheets can bring a large capacity of 515 mAh g–1 even after 2000 cycles under 10 A g–1. Additionally, as revealed by calculations and in situ/ex situ technique analysis, a favorable mechanism of Na+ intercalation/deintercalation into/from the GeS2 interlayer region (GeS2 ↔ NaxGeS2) is demonstrated. Furthermore, when coupled with the advanced cathode of Na3V2(PO4)2O2F, the sodium-ion full cell shows a stable high energy density (213 Wh kg–1), which makes our ultrathin GeS2 nanosheets a promising candidate for SIBs.
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