Related Experiment Video
Updated: Jun 4, 2025

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
Published on: May 20, 2019
A Dual-Functional Sulfur-Rich Copolymers for Stable Anchoring and Enhanced Conversion of Polysulfide in
Yao Fu1, Yang Jin1, Fang-Fei Guo1
1State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Dalian, Liaoning, 116024, China.
Abstract:
Sulfur-rich copolymers have gained a great deal of attention as promising cathode materials in Li-S batteries due to their low cost and naturally uniform sulfur dispersion. However, the poor electrical conductivity and shuttle effect cause rapid capacity decay and low sulfur utilization especially under high sulfur loading and low electrolyte/sulfur ratio. Herein, the Fe1-xS/C dispersed and Se-containing sulfur-rich copolymer (FSP) was synthesized by one-pot reaction of ferrocene, trithiocyanuric acid with SexSy. In such process, the trithiocyanuric acid reacts with SexSy to form Se-containing sulfur-rich copolymers. Simultaneously, ferrocene reacts with sulfur to form highly dispersed Fe1-xS/C within sulfur-rich copolymers. The covalent chemical binding of sulfur in the FSP effectively suppress the shuttle effect of polysulfides by chemical binding. Meanwhile, the Se improves the conductivity of FSP, which enhances the reaction kinetics. Moreover, the highly dispersed Fe1-xS/C in the FSP is able to effectively catalyze polysulfide conversion and inhibit the shuttle effect. As a result, the optimized FSP electrode exhibits a high capacity of 1330 mAh g-1 at 0.2 C. Even under high sulfur loading (4.08 mg cm-2) and low E/S ratio (6 μL mg-1), the FSP cathode demonstrates a remarkable capacity of 734.7 mAh g-1 at 0.2 C.
Related Concept Videos
Preparation and Reactions of Sulfides
Structure and Nomenclature of Thiols and Sulfides
Batteries and Fuel Cells
Formation of Complex Ions
Preparation and Reactions of Thiols
Electrophilic Aromatic Substitution: Sulfonation of Benzene

