In Situ Electrochemical Evolution of Amorphous Metallic Borides Enabling Long Cycling Room-/Subzero-Temperature Sodium-Sulfur Batteries

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2024) vom: 16. Okt., Seite e2411725
1. Verfasser: Wang, Bin (VerfasserIn)
Weitere Verfasser: Wang, Lu, Guo, Beining, Kong, Yueyue, Wang, Fengbo, Jing, Zhongxin, Qu, Guangmeng, Mamoor, Muhammad, Wang, Dedong, He, Xiyu, Kong, Lingtong, Xu, Liqiang
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article amorphous metallic borides catalytic activity electrochemical evolution room‐/subzero‐temperature
Beschreibung
Zusammenfassung:© 2024 Wiley‐VCH GmbH.
Room temperature sodium-sulfur batteries (RT Na-S) have garnered significant attention for their high energy density and cost-effectiveness, positioning them as a promising alternative to lithium-ion batteries. However, they encounter challenges such as the dissolution of sodium polysulfides and sluggish kinetics. Introducing high-activity electrocatalysts and enhancing the density of active sites represents an efficient strategy to enhance reaction kinetics. Here, an amorphous Ni-B material that undergoes electrochemical evolution to generate the NiSx phase within an operational sodium-sulfur battery, contrasting with the crystalline NiB counterpart is fabricated. Electrochemical cycling facilitated the establishment of an interface between the amorphous Ni-B and NiSx, leading to heightened catalytic activity and improved reaction kinetics. Consequently, batteries utilizing the amorphous Ni-B showcased a notable initial specific capacity of 1487 mAh g-1 at 0.2 A g-1, exhibiting exceptional performance under high current densities of 5 A g-1, in low-temperature conditions (-10 °C), with high sulfur loading, and in pouch cell configurations
Beschreibung:Date Revised 16.10.2024
published: Print-Electronic
Citation Status Publisher
ISSN:1521-4095
DOI:10.1002/adma.202411725