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

Yinger Xiang; Laiqiang Xu; Li Yang; Yu Ye; Zhaofei Ge; Jiae Wu; Wentao Deng; Guoqiang Zou; Hongshuai Hou; Xiaobo Ji

doi:10.1007/s40820-022-00873-x

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

Nanomicro Lett. 2022 Jun 17;14(1):136. doi: 10.1007/s40820-022-00873-x.

Authors

Yinger Xiang¹, Laiqiang Xu¹, Li Yang², Yu Ye¹, Zhaofei Ge¹, Jiae Wu¹, Wentao Deng¹, Guoqiang Zou¹, Hongshuai Hou³, Xiaobo Ji^{1

4}

Affiliations

¹ College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, People's Republic of China.
² College of Science, Hunan University of Technology and Business, Changsha, 410205, People's Republic of China.
³ College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, People's Republic of China. hs-hou@csu.edu.cn.
⁴ School of Material Science and Engineering, Zhengzhou University, Zhengzhou, 450001, People's Republic of China.

Abstract

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.

Keywords: Anode; Carbon dots; Initial Coulombic efficiency; Interfacial bond; Sb2S3.