Affiliation:
1. Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of Education School of Physics and Electronic Engineering Harbin Normal University Harbin 150025 P. R. China
2. School of Physics and Electronic Engineering Northeast Petroleum University Daqing 163318 P. R. China
3. Frontiers Science Center for Flexible Electronics and Xi'an Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 P. R. China
Abstract
AbstractLithium–sulfur batteries (LSBs) currently face challenges including lithium polysulfide shuttling, sluggish sulfur redox kinetics, severe lithium dendrite growth, and volume change. Herein, an advanced dual‐functional host is designed by embedding 3D N‐doped carbon fibers with abundant 2D V2CTx nanosheets (N/CF@V2CTx). The N‐doped carbon fibers act as “thread” to connect the V2CTx nanosheets and form a unique open 3D macroporous structure. This structure effectively prevents the restacking of the V2CTx nanosheets and exposes their lithiophilic and sulfurophilic sites. Consequently, the N/CF@V2CTx host effectively suppresses the shuttling of LiPSs and improves the cathodic kinetics. Furthermore, the 3D‐ordered porous skeleton integrated with abundant lithophilic sites enables uniform Li deposition and homogeneous Li‐ion flux, thereby inhibiting dendrite growth and mitigating volume expansion. The as‐assembled LSBs exhibit excellent rate capability (640 mAh g−1 at 15 C) and outstanding cycling stability (0.019% capacity decay per cycle throughout 1200 cycles at 1 C). Moreover, the pouch cell assembled with the N/CF@V2CTx host demonstrates a high energy density of 350 Wh kg−1 and good cycling stability. This research presents a promising approach to address the challenges of both the sulfur cathode and the lithium anode comprehensively and effectively in working LSBs.
Funder
National Natural Science Foundation of China
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
16 articles.
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