双金属片
兴奋剂
碳纤维
阳极
离子
材料科学
钠
硫化物
化学工程
硫化钠
无机化学
化学
电极
光电子学
冶金
物理化学
复合数
金属
复合材料
有机化学
工程类
作者
Chao Li,Shunan Ke,Sihan Liu,Ge Wu,Qing Li,Yu Zhang,Kangzhe Cao
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-07-20
被引量:2
标识
DOI:10.1021/acs.langmuir.4c01760
摘要
Benefiting from its high theoretical capacity, tin disulfide (SnS2) draws abundant interest and attention for its promising practical prospect for sodium-ion batteries (SIBs). However, the huge volumetric variation in sodiation/desodiation reactions usually results in the fast decay of rate and cycling properties, which seriously obstructs its future applicable foregrounds. Herein, heterostructured Mn-Sn bimetallic sulfide nanocubes confined in N and S-codoped carbon (MSS@NSC) were rationally designed via a facile coprecipitation followed by a sulfurization strategy. When used as anodes for SIBs, the heterojunctions at the interfaces effectively accelerate the Na+ diffusion rate to promote the sodium-storage reaction kinetics. The N and S-codoped carbon provides a rapid conductive framework for the fast charge transport during the sodium-storage process. Moreover, the beneficial confinement effect of the NSC layer effectively guarantees a superb cycle property for the MSS@NSC anode. The favorable synergistic effects between the highly conductive framework of the NSC and MSS heterostructure endow the MSS@NSC anode with satisfactory electrochemical Na-storage properties.
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