Experimental and Theoretical Insights on Interface Engineered FeS/rGO as Anode for Fast-Charging Lithium- and Sodium-Ion Batteries

被引:0
|
作者
Vishwanathan, Savithri [1 ,2 ]
Mohanta, Manish Kumar [3 ]
Jena, Puru [3 ]
Matte, H. S. S. Ramakrishna [1 ,2 ]
机构
[1] Ctr Nano & Soft Matter Sci CeNS, Energy Mat Lab, Bengaluru 562162, India
[2] Manipal Acad Higher Educ MAHE, Manipal 576104, India
[3] Virginia Commonwealth Univ, Dept Phys, Richmond, VA 23284 USA
关键词
anode; diffusion energy; interface engineering; lithium-ion batteries; sodium-ion batteries; HIGH-RATE PERFORMANCE; RAMAN-SPECTROSCOPY; COMPOSITE; SURFACE;
D O I
10.1002/smll.202410482
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Interface engineering facilitates the development of stable energy storage devices that can endure the severe changes encountered during operation. In the context of fast-charging anodes for lithium- and sodium-ion batteries (LIBs and SIBs), the interface needs to promote charge/ion transfer processes, enhance Li-/Na-ion storage capacity, and ensure good reversibility in order to function efficiently at high rates. Herein, a simple synthetic strategy is reported to design interfaces between transition metal sulfides and carbonaceous supports to generate high-performance fast-charging anodes. FeS/rGO nanostructures are synthesized via a simple solid-state annealing method by employing FeOOH/rGO, a metastable precursor, which is annealed at 600 degrees C in the presence of H2S gas. Interface engineering between FeS and rGO significantly improved the electrochemical performance, particularly demonstrated by stable capacities at high rates (625 mAh g(-)(1) at 5 A g(-)(1) for LIBs and 708 mAh g(-)(1) at 10 A g(-)(1) for SIBs). The high-rate charge storage is primarily governed by capacitive processes. Density functional theory (DFT) calculations attributed the enhanced performance of the FeS/rGO anode to a lower diffusion energy barrier for Li- and Na-ion diffusion at the interface along with the presence of a built-in electric field at the heterointerface.
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页数:10
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