Polysulfide Rejection Strategy in Lithium-Sulfur Batteries Using an Ion-Conducting Gel-Polymer Interlayer Membrane.

ACS Appl Mater Interfaces

Ionic Liquid and Solid-State Ionics Laboratory, Department of Physics, Institute of Science, Banaras Hindu University, Varanasi 221005, India.

Published: July 2023

AI Article Synopsis

  • Lithium-sulfur batteries (LiSBs) offer advantages like high energy density, low cost, and eco-friendliness compared to conventional lithium-ion batteries (LiBs), but face challenges due to polysulfide dissolution.
  • Researchers developed a lithium salt and ionic liquid solution impregnated gel-polymer membrane (IC-GPM70) to prevent polysulfide migration, allowing only lithium ions to move while trapping polysulfides.
  • The IC-GPM70 interlayer significantly enhances the stability and performance of LiSBs, achieving higher cycling stability (1200 cycles) and better rate performance than batteries without this interlayer, making LiSBs more viable for commercial use.

Article Abstract

Lithium-sulfur batteries (LiSBs) are emerging as promising alternative to conventional secondary lithium-ion batteries (LiBs) due to their high energy density, low cost, and environmental friendliness. However, preventing polysulfide dissolution is a great challenge for their commercial viability. The present work is focused on preparing a lithium salt and ionic liquid (IL) solution (SIL) impregnated ion (lithium ion)-conducting gel-polymer membrane (IC-GPM) interlayer to prevent polysulfide migration toward the anode by using an electrostatic rejection and trapping strategy. Herein, we introduce an SIL-based freestanding optimized IC-GPM70 (70 wt % SIL) interlayer membrane with high lithium-ion conductivity (2.58 × 10 S cm) along with excellent thermal stability to suppress the migration of polysulfide toward the anode and prevent polysulfide dissolution in the electrolyte. Because of the coulombic interaction, the anionic groups, -CF of the β-phase polymer host PVdF-HFP, TFSI anion of IL EMIMTFSI, and anion BOB of LIBOB salt, allow hopping of positively charged lithium ions (Li) but reject negatively charged and relatively large-sized polysulfide anions (S, 4 < <8). The cationic group EMIM of the IL is electrostatically able to attract and trap the polysulfides in the interlayer membrane. Since the shuttle effect of lithium polysulfides in LiSBs has been suppressed by the prepared IC-GPM70 interlayer, the resulting lithium-sulfur cell exhibits significantly higher cycling stability (1200 cycles), rate performance (1343, 1208, 1043, 875, and 662 mAh g at 0.1C, 0.2C, 0.5C, 1C, and 2C, respectively), and structural integrity during cycling than its counterpart without the IC-GPM70 interlayer. The interlayer membrane has been found to improve the performance and durability of LiSBs, thus making them a viable alternative to conventional LiBs.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.3c02800DOI Listing

Publication Analysis

Top Keywords

lithium-sulfur batteries
8
ion-conducting gel-polymer
8
interlayer membrane
8
polysulfide dissolution
8
prevent polysulfide
8
polysulfide
6
polysulfide rejection
4
rejection strategy
4
strategy lithium-sulfur
4
batteries ion-conducting
4

Similar Publications

Graphene quantum dot-modified CoO/NiCoO yolk-shell polyhedrons as a polysulfide-adsorptive sulfur host for lithium-sulfur batteries.

Chem Commun (Camb)

January 2025

Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241002, P. R. China.

The shuttle effect of lithium polysulfides and non-ideal reaction kinetics restrict the development of high-energy-density lithium-sulfur (Li-S) batteries. Here, we report a graphene quantum dot (GQD)-modified CoO/NiCoO yolk-shell polyhedron as a sulfur host for Li-S batteries. GQDs shorten transport pathways of electrons, while strong binding of CoO and NiCoO to LiS, LiS and LiS are demonstrated from density functional theory calculations.

View Article and Find Full Text PDF

Developing high-energy-density lithium-sulfur batteries faces serious polysulfide shuttle effects and sluggish conversion kinetics, often necessitating the excessive use of electrolytes, which in turn adversely affects battery performance. Our study introduces a meticulously designed electrocatalyst, Cu-CeO@N/C, to enhance lean-electrolyte lithium-sulfur battery performance. This catalyst, featuring in situ synthesized Cu clusters, regulates oxygen vacancies in CeO and forms Cu-CeO heterojunctions, thereby diminishing sulfur conversion barriers and hastening reaction kinetics through the generation of S/S intermediates.

View Article and Find Full Text PDF

Biomimetic calcification is a micro-crystallization process that mimics the natural biomineralization process, where biomacromolecules regulate the formation of inorganic minerals. In this study, it is presented that a protein-assisted biomimetic calcification method for the in situ synthesis of nitrogen-doped metal-organic framework (MOF) materials. A series of unique core-shell structures are created by utilizing proteins as templates and guiding agents in the nucleation step, creating ideal conditions for shell growth.

View Article and Find Full Text PDF

Magnetopyrite FeS modified with N/S-doped carbon as a synergistic electrocatalyst for lithium-sulfur batteries.

J Colloid Interface Sci

January 2025

College of Physics and Electronic Information, Yunnan Normal University, 650500 Kunming, China. Electronic address:

Rational design of effective cathode host materials is an effective way to solve the problems of serious shuttle and slow conversion of polysulfides in lithium-sulfur batteries (LSBs). However, the redox reaction of sulfur differs from conventional "Rocking chair" type batteries and involves a cumbersome phase transition process, so a single-component catalyst cannot consistently and steadily enhance the reaction rate throughout the redox process. In this work, a hybrid composed of magnetopyrite FeS catalyst-modified with N/S-doped porous carbon spheres (FeS@NSC) is proposed as a novel sulfur host to synergistically promote the adsorption and redox catalysis conversion of polysulfides.

View Article and Find Full Text PDF

Sulfur conversion reactions are the foundation of lithium-sulfur batteries but usually possess sluggish kinetics during practical battery operation. Herein, a high-entropy single-atom catalyst (HESAC) is synthesized for this process. In contrast to conventional dual-atom catalysts that form metal-metal bonds, the center metal atoms in HESAC are not bonded but exhibit long-range interactions at a sub-nanometer distance (<9 Å).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!