Two-Dimensional SnO Anodes with a Tunable Number of Atomic Layers for Sodium Ion Batteries
KAUST DepartmentImaging and Characterization Core Lab
Materials Science and Engineering Program
Physical Sciences and Engineering (PSE) Division
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AbstractWe have systematically changed the number of atomic layers stacked in 2D SnO nanosheet anodes and studied their sodium ion battery (SIB) performance. The results indicate that as the number of atomic SnO layers in a sheet decreases, both the capacity and cycling stability of the Na ion battery improve. The thinnest SnO nanosheet anodes (two to six SnO monolayers) exhibited the best performance. Specifically, an initial discharge and charge capacity of 1072 and 848 mAh g-1 were observed, respectively, at 0.1 A g-1. In addition, an impressive reversible capacity of 665 mAh g-1 after 100 cycles at 0.1 A g-1 and 452 mAh g-1 after 1000 cycles at a high current density of 1.0 A g-1 was observed, with excellent rate performance. As the average number of atomic layers in the anode sheets increased, the battery performance degraded significantly. For example, for the anode sheets with 10-20 atomic layers, only a reversible capacity of 389 mAh g-1 could be obtained after 100 cycles at 0.1 A g-1. Density functional theory calculations coupled with experimental results were used to elucidate the sodiation mechanism of the SnO nanosheets. This systematic study of monolayer-dependent physical and electrochemical properties of 2D anodes shows a promising pathway to engineering and mitigating volume changes in 2D anode materials for sodium ion batteries. It also demonstrates that ultrathin SnO nanosheets are promising SIB anode materials with high specific capacity, stable cyclability, and excellent rate performance.
CitationZhang F, Zhu J, Zhang D, Schwingenschlögl U, Alshareef HN (2017) Two-Dimensional SnO Anodes with a Tunable Number of Atomic Layers for Sodium Ion Batteries. Nano Letters 17: 1302–1311. Available: http://dx.doi.org/10.1021/acs.nanolett.6b05280.
SponsorsResearch reported in this manuscript was supported by funding from King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia. F.Z. acknowl- edges supports from the KAUST Graduate Fellowship. F.Z. also thanks Dr. Hanfeng Liang, Mr. Guan Sheng, Dr. Bilal Ahmed, Mr. Qiu Jiang and Dr. Dhinesh Velusamy for their help. Figures 1b and 5a were produced by Mr. Heno Hwang, scientific illustrator at King Abdullah University of Science and Technology (KAUST).
PublisherAmerican Chemical Society (ACS)