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Investigation of electrochemical reaction mechanism for antimony selenide nanocomposite for sodium-ion battery electrodes

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Abstract

Antimony selenide and its carbon composite were synthesized through a mechanochemical process and investigated as anode materials for sodium-ion secondary batteries. X-ray diffraction (XRD) with rietveld refinement and transmission electron microscopy (TEM) analyses confirm that Sb2Se3 were composed of agglomerated highly crystalline nanocrystallites and the Sb2Se3/C composite consisted of nanocrystalline Sb2Se3 dispersed homogeneously throughout an amorphized carbon matrix. The initial Coulombic efficiency, rate capability, and cycle performance of the Sb2Se3/C composite were superior to those of Sb, or Sb2Se3. The Sb2Se3/C composite, in particular, showed excellent cycle stability, with 98.2% of initial capacity at 200 mA g−1 after 200 cycles. Based on the reaction potentials, ex situ XRD patterns and ex situ HR-TEM analysis of the Sb2Se3/C composite electrode revealed the structural changes which occurred reversibly within the Sb2Se3/C composite by conversion and recombination reaction during sodiation and desodiation process. Furthermore, XPS analysis study was carried out for identifying the surface films formed on both the electrodes and their effects on the performances.

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Acknowledgements

This work was supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (No. 20152020105420). This research was supported by Technology Development Program to Solve Climate Changes through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT (No. 2018M1A2A2063343).

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Correspondence to Jeong-Hee Choi or Cheol-Min Park.

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Choi, JH., Lee, MH., Choi, HY. et al. Investigation of electrochemical reaction mechanism for antimony selenide nanocomposite for sodium-ion battery electrodes. J Appl Electrochem 49, 207–216 (2019). https://doi.org/10.1007/s10800-018-1267-2

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  • DOI: https://doi.org/10.1007/s10800-018-1267-2

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