Electrochemical release of catalysts in nanoreactors for solid sulfur redox reactions in room-temperature sodium-sulfur batteries

Autor: Weihong Lai, Jian Peng, Akhil Tayal, Hua-Kun Liu, Zichao Yan, Shulei Chou, Wanlin Wang, Weibo Hua, Jian Liu, Yunxiao Wang, Gao Qing Lu, Yaru Liang, Zhe Hu, Lingyan Jing, Qiang Tian, Shi Xue Dou
Přispěvatelé: Lu, Gao-Qing
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: Cell Reports Physical Science, Vol 2, Iss 8, Pp 100539-(2021)
Cell reports 2(8), 100539 (2021). doi:10.1016/j.xcrp.2021.100539
Cell reports, 2 (8), Art.Nr.: 100539
ISSN: 2666-3864
DOI: 10.1016/j.xcrp.2021.100539
Popis: Cell reports 2(8), 100539 (2021). doi:10.1016/j.xcrp.2021.100539
Electrocatalysis-assisted entrapment of polysulfide while ensuring efficient nucleation of Na$_2$S holds the key to addressing the shuttle effect and sluggish kinetics of polysulfide in room-temperature (RT) Na/S batteries. The constrained active sites, however, dramatically limit the efficiency of electrocatalysts. Here, a strategy of electrochemically releasing nano-silver catalytic sites during the discharge process is presented, visualized, and implemented for accelerated Na$_2$S nucleation. Because of the effective polysulfide immobilization and accelerated Na$_2$S nucleation, the sulfur cathode, supported by a self-released silver electrocatalyst, exhibits a superior reversible capacity of 701 mAh g$^{���1}$ at 0.1 A g$^{���1}$ and an ultra-stable cycling performance. Precise understanding of the electrochemically self-releasing mechanism and the catalysis in Na$_2$S nucleation via in situ transmission electron microscopy (TEM) would aid, however, in fundamentally optimizing the working mechanism and for further development of more stable high-power RT Na/S batteries.
Published by Elsevier, [New York, NY]
Databáze: OpenAIRE