Organosulfur‐Rich Porous Carbon Cathode Enables Soluble‐Polysulfide‐Free and High‐Rate Potassium‐Sulfur Batteries

X Xuanhua Chen (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) T Tan Yi (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) Z Zongheng Cen (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) X Xiaoyu Qiao (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) Y Yiwei Ji (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) R Ruowen Fu (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) J Junlong Huang (Advanced Institute for Materials Research (WPI‐AIMR) Tohoku University Sendai 980‐8577 Japan) S Shaohong Liu (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China)

Abstract

Abstract Potassium–sulfur (K–S) batteries are emerging as one of the most promising candidates for next‐generation energy storage, owing to their high energy density and cost‐effectiveness. However, the severe polysulfide shuttle effect and sluggish redox kinetics of sulfur cathodes remain critical barriers to their practical application. Herein, a class of organosulfur‐rich porous carbon (OSPC) has been developed as a high‐performance cathode for soluble‐polysulfide‐free and high‐rate K–S batteries. The as‐constructed OSPC achieves molecular‐scale confinement of sulfur species within the carbon skeleton via covalent bonding, which enables solid–solid sulfur redox pathways without generation of electrolyte‐soluble polysulfides. Moreover, the conductive carbon skeleton of OSPC with well‐developed porosity can facilitate potassium ion and electron transport within the bulk cathode and significantly improve sulfur redox kinetics. Benefiting from these integrated merits, excellent high rate capability (240.8 mAh g −1 at 5 A g −1 based on the mass of OSPC), long‐term cycling stability (77% retention after 500 cycles at 5 A g −1 ), and remarkable areal capacity (4.5 mAh cm −2 ) can be achieved for the OSPC cathodes. Additionally, the feasibility of synthesizing OSPC from real‐world waste plastics is demonstrated, which offers a dual benefit of alleviating plastic pollution and enabling the fabrication of low‐cost yet high‐performance cathodes for K–S batteries.

Article Details

Volume / Issue Vol. 65, Issue 2
Published January 09, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

X

Xuanhua Chen

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

T

Tan Yi

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

Z

Zongheng Cen

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

X

Xiaoyu Qiao

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

Y

Yiwei Ji

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

R

Ruowen Fu

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

J

Junlong Huang

Advanced Institute for Materials Research (WPI‐AIMR) Tohoku University Sendai 980‐8577 Japan

S

Shaohong Liu

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China