Room-temperature sodium-sulfur (RT Na-S) batteries have recently captured intensive research attention from the community and are regarded as one of promising next-generation energy storage devices since they not only integrate the advantages in high abundance and low commercial cost of elemental Na/S but also exhibit exceptionally high theoretical capacity and energy density. Whereas, the notorious shuttle effect of soluble intermediates and sluggish kinetics remain two main obstacles for RT Na-S batteries to step into new developmental stage. Recently, impressive advancements of metal-based electrocatalysts have offered a viable solution to stabilize S cathodes and unlocked new opportunities for RT Na-S batteries. Here, we underline the recent progress on metal-based electrocatalysts for RT Na-S batteries for the first time by shedding light on this emerging but promising field. The involved metal-based electrocatalysts include metals, metal oxides, metal sulfides, metal carbides, and other metal-based catalytic species. Our emphasis is focused on the discussion of design, fabrication, and properties of these electrocatalysts as well as interactions between electrocatalysts and sodium polysulfides. Otherwise, some potential electrocatalysts for RT Na-S batteries are pointed out as well. At last, perspectives for the future development of RT Na-S batteries with S cathode electrocatalysts are offered.
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http://dx.doi.org/10.1039/d1mh01326b | DOI Listing |
Adv Sci (Weinh)
January 2025
Institute for Superconducting & Electronic Materials (ISEM), Faculty of Engineering and Information Sciences (EIS), University of Wollongong, Wollongong, NSW, 2500, Australia.
Rechargeable batteries are central to modern energy storage systems, from portable electronics to electric vehicles. The cathode material, a critical component, largely dictates a battery's energy density, capacity, and overall performance. This review focuses on the application of operando X-ray absorption spectroscopy (XAS) to study cathode materials in Li-ion, Na-ion, Li-S, and Na-S batteries.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
School of Materials and Energy, and LONGi Institute of Future Technology, Lanzhou University, Lanzhou 730000 China. Electronic address:
Room-temperature sodium-sulfur (RT Na-S) batteries, known for their high-energy density, low cost and environmental friendliness, have attracted much attention. However, the development of RT Na-S batteries has encountered a number of challenges, including low conductivity and large volume changes of sulfur during the charge-discharge cycles. In this study, TiO nanoparticles modified porous carbon hosts for sulfur in RT Na-S batteries were prepared by a simple and efficient spray drying method combined with solution immersion.
View Article and Find Full Text PDFACS Nano
January 2025
Soft Foundry Institute, Seoul National University, Seoul 08826, Republic of Korea.
Nickel-rich NCM cathode materials promise lithium-ion batteries with a high energy density. However, an increased Ni fraction in the cathode leads to complex phase transformations with electrode-electrolyte side reactions, which cause rapid capacity fading. Here, we show that an initial formation cycle at 0.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute of Energy Materials Science (IEMS), University of Shanghai for Science and Technology, Shanghai 200093, China.
Room-temperature sodium-sulfur (RT Na-S) batteries that typically feature multielectron conversion chemistries can allow an ultrahigh specific capacity of 1675 mA h g and a high energy density of 1275 W h kg but unfortunately suffer from a lot of intractable challenges from sulfur cathodes. These issues cover the poor electronic conductivity of pristine sulfur and solid products, the severe shuttle effect of polysulfides, and the sluggish redox kinetics, The shuttling behavior of polysulfides always leads to cathode/anode instability and performance degeneration. Recently, the emerging catalysis strategy has been demonstrated as a reliable pathway to tackle the central issues caused by sulfur electrochemistry and revitalize RT Na-S batteries.
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.
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