1. Natural Stibnite for Lithium-/Sodium-Ion Batteries: Carbon Dots Evoked High Initial Coulombic Efficiency.
- Author
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Xiang Y, Xu L, Yang L, Ye Y, Ge Z, Wu J, Deng W, Zou G, Hou H, and Ji X
- Abstract
Highlights: The chemical process of local oxidation-partial reduction-deep coupling for stibnite reduction of carbon dots (CDs) is revealed by in-situ high-temperature X-ray diffraction. Sb
2 S3 @xCDs anode delivers high initial coulombic efficiency in lithium ion batteries (85.2%) and sodium ion batteries (82.9%), respectively. C-S bond influenced by oxygen-rich carbon matrix can restrain the conversion of sulfur to sulfite, well confirmed by X-ray photoelectron spectroscopy characterization of solid electrolyte interphase layers helped with density functional theory calculations. CDs-induced Sb-O-C bond is proved to effectively regulate the interfacial electronic structure. The application of Sb2 S3 with marvelous theoretical capacity for alkali metal-ion batteries is seriously limited by its poor electrical conductivity and low initial coulombic efficiency (ICE). In this work, natural stibnite modified by carbon dots (Sb2 S3 @xCDs) is elaborately designed with high ICE. Greatly, chemical processes of local oxidation-partial reduction-deep coupling for stibnite reduction of CDs are clearly demonstrated, confirmed with in situ high-temperature X-ray diffraction. More impressively, the ICE for lithium-ion batteries (LIBs) is enhanced to 85%, through the effect of oxygen-rich carbon matrix on C-S bonds which inhibit the conversion of sulfur to sulfite, well supported by X-ray photoelectron spectroscopy characterization of solid electrolyte interphase layers helped with density functional theory calculations. Not than less, it is found that Sb-O-C bonds existed in the interface effectively promote the electronic conductivity and expedite ion transmission by reducing the bandgap and restraining the slip of the dislocation. As a result, the optimal sample delivers a tremendous reversible capacity of 660 mAh g-1 in LIBs at a high current rate of 5 A g-1 . This work provides a new methodology for enhancing the electrochemical energy storage performance of metal sulfides, especially for improving the ICE., (© 2022. The Author(s).)- Published
- 2022
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