Natural Stibnite for Lithium-/Sodium-Ion Batteries: Carbon Dots Evoked High Initial Coulombic Efficiency

离子 法拉第效率 化学 碳纤维 锂(药物) 辉锑矿 材料科学 电极 矿物学 物理化学 电化学 有机化学 复合材料 内科学 黄铁矿 闪锌矿 复合数 医学
作者
Yinger Xiang,Laiqiang Xu,Yang Li,Yu Ye,Zhaofei Ge,Jiae Wu,Wentao Deng,Guoqiang Zou,Hongshuai Hou,Xiaobo Ji
出处
期刊:Nano-micro Letters [Springer Nature]
卷期号:14 (1) 被引量:74
标识
DOI:10.1007/s40820-022-00873-x
摘要

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. Sb2S3@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 Sb2S3 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 (Sb2S3@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.
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