Porous Carbon Cloth@CoSe2 as Kinetics‐Enhanced and High‐Loading Integrated Sulfur Host for Lithium–Sulfur Batteries
Source abstract
Abstract
Abstract Carbon cloth (CC) possesses great potential as a sulfur host because of its excellent conductivity, flexibility, and easily modified free‐standing structure. However, the previous works do not take full advantage of CC except for the role of support and current collector. The smooth surface, small specific surface area, and poor binding force between coating materials and CC matrix are unfavorable for loading coating materials. The slow redox kinetics and low sulfur loading of sulfur cathodes still seriously restrict the development of Lithium–Sulfur (Li–S) batteries. Herein, the porous carbon cloth loading cobalt selenide (PCC@CoSe2) is constructed as an integrated sulfur host through a pore‐creating and selenylation strategy. The pore‐creating engineering greatly optimizes the 3D pore structure of CC to raise the sulfur and catalyst loading and provides enough space to accommodate the volume change of sulfur species. In addition, CoSe2 particles as nano‐catalyst units embedded in PCC can effectively adsorb‐catalyze polysulfides and improve the reaction kinetics. The resulting integrated sulfur cathode has realized the high‐efficiency polysulfide catalytic conversion and fast lithium ion migration, significantly enhancing redox kinetics and sulfur loading.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Organic Electronics and Information Displays & Institute of Advanced Materials (IAM) Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM) Nanjing University of Posts & Telecommunications 9 Wenyuan Road Nanjing 210023 China
Department of Chemical and Biological Engineering University at Buffalo The State University of New York Buffalo NY 14260 USA
Funding
National Natural Science Foundation of China · Nanjing University of Posts and Telecommunications
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