April 7 - 11, 2025
Seattle, Washington
Symposium Supporters
2025 MRS Spring Meeting & Exhibit
EN01.10.29

Investigation of Vanadium Pentoxide–Sulfur Cathodes for Enhanced Lithium–Sulfur Battery Performance

When and Where

Apr 9, 2025
5:00pm - 7:00pm
Summit, Level 2, Flex Hall C

Presenter(s)

Co-Author(s)

Sunny Choudhary1,Shweta Shweta1,Satyam Kumar1,Shivaraju Chandrappa1,Ivan Castillo1,2,3,Balram Tripathi1,4,Gerardo Morell1,Ram Katiyar1

University of Puerto Rico1,University of Puerto Rico at Cayey2,Ana G Mendez Cupey University3,S S Jain Subodh P.G.(Auto.) College, Jaipur, Rajasthan, India4

Abstract

Sunny Choudhary1,Shweta Shweta1,Satyam Kumar1,Shivaraju Chandrappa1,Ivan Castillo1,2,3,Balram Tripathi1,4,Gerardo Morell1,Ram Katiyar1

University of Puerto Rico1,University of Puerto Rico at Cayey2,Ana G Mendez Cupey University3,S S Jain Subodh P.G.(Auto.) College, Jaipur, Rajasthan, India4
Lithium–sulfur batteries (LSBs), widely regarded as a promising next-generation energy storage system due to their high theoretical specific capacity and environmental compatibility, remain constrained by the insulating nature of sulfur and the shuttle effect of soluble long-chain polysulfides. Here, we report the multiwalled carbon nanotube sulfur (S)/(MWCNT)/vanadium pentoxide (V2O5) composite prepared via a tube-furnace encapsulation process in an argon atmosphere that effectively addresses these shortcomings. In this design, MWCNTs establish a robust electron conduction framework, while polar V2O5 sequesters polysulfides, thereby mitigating their dissolution into the electrolyte. Electrochemical tests demonstrate that the encapsulated S/MWCNT/ V2O5/CMC electrode achieves a specific capacity of 1605 mAh g-1 at 0.1C, a substantial improvement over pristine S/MWCNT/CMC electrodes, which delivered ~550 mAh g-1 at 0.5C and are prone to short circuits at higher current densities. The V2O5-encapsulated electrodes also retain significant performance, exhibiting capacities of 750 mAh g-1 at 1C after 80 cycles and 600 mAh g-1 at 0.5C after 120 cycles, surpassing unencapsulated MWCNT/ V2O5 (initial capacity ~1203 mAh g-1 at C/20). Cyclic voltammetry and electrochemical impedance spectroscopy further demonstrate enhanced redox kinetics and reduced interfacial resistance. Overall, our work highlights a robust strategy to overcome critical barriers in LSBs technology, paving the way for high-capacity, long-life energy storage systems. We will present these findings in detail, including XPS, XRD, Raman, TGS, and DSC analyses, at the conference.

Keywords

intercalated | S

Symposium Organizers

Junjie Niu, University of Wisconsin--Milwaukee
Ethan Self, Oak Ridge National Laboratory
Shuya Wei, University of New Mexico
Ling Fei, The University of Louisiana at Lafayette

Symposium Support

Bronze
BioLogic
Neware Technology LLC

Session Chairs

Junjie Niu
Ethan Self

In this Session