Lithium-sulfur (Li-S) batteries have attracted all-time attention because of their supernormal high energy density and low cost, whereas they are still plagued by the severe polysulfide shuttling and sluggish sulfur redox reaction kinetics. Moreover, poor sulfur electrochemical utilization and rapid capacity degradation are top concerns in the high-loading Li-S batteries, which severely hinder their practical applications. Herein, a completely novel porous nanoneedle array NiCoS electrocatalyst grown on a nitrogen-sulfur-doped carbon cloth (NSCC) (NiCoS@NSCC) is constructed as a 3D self-supported sulfur host for high-loading Li-S batteries, in which the highest sulfur loading reaches 4.9 mg cm. The as-prepared NiCoS@NSCC with a typical sulfur loading of around 2.0 mg cm provides a high discharge capacity of 1223 mA h g at 0.2 C and long-term cycle stability with a low capacity decay of 0.046% per cycle over 500 cycles at 1 C. Additionally, NiCoS@NSCC/S with a high sulfur loading of 4.9 mg cm delivers an excellent reversible areal capacity of 4.4 mA h cm g over 50 cycles. Noting that such superior electrochemical performance of NiCoS@NSCC/S with high-loading sulfur is mainly attributed to high electronic conductivity and the abundant porous structure of NSCC to transport electrons and ions fastly and accommodate sulfur as well as robust absorbability and the outstanding catalytic effect of NiCoS to accelerate the capture and conversion of the polysulfide intermediate. Predictably, this work can provide a guideline to efficiently and rationally design the structure of metal-based compounds with catalytic functions for various applications.
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http://dx.doi.org/10.1021/acsami.0c20519 | DOI Listing |
Molecules
December 2024
Shanxi Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.
Lithium-sulfur (Li-S) batteries have emerged as a promising candidate for next-generation high-energy rechargeable lithium batteries, but their practical application is impeded by the sluggish redox kinetics and low sulfur loading. Here, we report the in situ growth of δ-MnO nanosheets onto hierarchical porous carbon microspheres (HPCs) to form an HPCs/S@MnO composite for advanced lithium-sulfur batteries. The delicately designed hybrid architecture can effectively confine LiPSs and obtain high sulfur loading up to 10 mg cm, in which the inner carbon microspheres with a large pore volume and large specific surface area can encapsulate high sulfur content, and the outer MnO nanosheets, as a catalytic layer, can improve the conversion reaction of LiPSs and suppress the shuttle effect.
View Article and Find Full Text PDFNat Mater
January 2025
Department of Mechanical Engineering, The Pennsylvania State University, University Park, PA, USA.
Lithium-sulfur (Li-S) all-solid-state batteries (ASSBs) hold great promise for next-generation safe, durable and energy-dense battery technology. However, solid-state sulfur conversion reactions are kinetically sluggish and primarily constrained to the restricted three-phase boundary area of sulfur, carbon and solid electrolytes, making it challenging to achieve high sulfur utilization. Here we develop and implement mixed ionic-electronic conductors (MIECs) in sulfur cathodes to replace conventional solid electrolytes and invoke conversion reactions at sulfur-MIEC interfaces in addition to traditional three-phase boundaries.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, China.
Single-atom catalysts (SACs) have become the forefront and hotspot in energy storage and conversion research, inheriting the advantages of both homogeneous and heterogeneous catalysts. In particular, carbon-supported SACs (CS-SACs) are excellent candidates for many energy storage and conversion applications, due to their maximum atomic efficiency, unique electronic and coordination structures, and beneficial synergistic effects between active catalytic sites and carbon substrates. In this review, we briefly review the atomic-level regulation strategies for optimizing CS-SACs for energy storage and conversion, including coordination structure control, nonmetallic elemental doping, axial coordination design, and polymetallic active site construction.
View Article and Find Full Text PDFChemSusChem
January 2025
Washington State University, School of Mechanical and Materials Engineering, PO Box 642920, 99164-2920, Pullman, UNITED STATES OF AMERICA.
Advancement of sulfur (S) cathode of lithium-sulfur (Li-S) batteries is hindered by issues such as insulating nature of sulfur, sluggish redox kinetics, polysulfide dissolution and shuttling. To address these issues, we initiate a study on applying an important amino acid of protein, arginine (Arg), as a functional additive into S cathodes. Based on our simulation study, the positively charged Arg facilitates strong interactions with polysulfides.
View Article and Find Full Text PDFNat Commun
January 2025
Faculty of Materials Science and Energy Engineering, Shenzhen University of Advanced Technology, Shenzhen, China.
Aqueous zinc ion batteries exhibit great prospects due to their low cost and high safety, while their lifespan is limited by severe dendritic growth problems. Herein, we develop an anti-dendrite hot-pressing separator interlayer through a mass-producible hot-pressing strategy, by spreading metal-organic framework (MOF) precursor on nonwoven matrix followed by a simple hot-pressing process. The in situ modification of MOF crystals on fiber surface processes abundant nitrogenous functional groups and high specific surface area (190.
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