| Literature DB >> 32203631 |
Meng Zhao1,2, Hong-Jie Peng3,4, Bo-Quan Li1,2,4, Xiao Chen3, Jin Xie3, Xinyan Liu3,4, Qiang Zhang3, Jia-Qi Huang1,2.
Abstract
In situ evolution of electrocatalysts is of paramount importance in defining catalytic reactions. Catalysts for aprotic electrochemistry such as lithium-sulfur (Li-S) batteries are the cornerstone to enhance intrinsically sluggish reaction kinetics but the true active phases are often controversial. Herein, we reveal the electrochemical phase evolution of metal-based pre-catalysts (Co4 N) in working Li-S batteries that renders highly active electrocatalysts (CoSx ). Electrochemical cycling induces the transformation from single-crystalline Co4 N to polycrystalline CoSx that are rich in active sites. This transformation propels all-phase polysulfide-involving reactions. Consequently, Co4 N enables stable operation of high-rate (10 C, 16.7 mA cm-2 ) and electrolyte-starved (4.7 μL mgS -1 ) Li-S batteries. The general concept of electrochemically induced sulfurization is verified by thermodynamic energetics for most of low-valence metal compounds.Entities:
Keywords: electrocatalysts; electrochemical phase evolution; lithium-sulfur batteries; polysulfide conversion
Year: 2020 PMID: 32203631 DOI: 10.1002/anie.202003136
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336