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Synthesis of yolk-shell-structured iron monosulfide-carbon microspheres and understanding of their conversion reaction for potassium-ion storage

Authors
Kim, Ju HyeongPark, Gi DaeKang, Yun Chan
Issue Date
8월-2021
Publisher
WILEY
Keywords
anode materials; iron monosulfide; potassium& #8208; ion batteries; yolk& #8208; shell microspheres
Citation
INTERNATIONAL JOURNAL OF ENERGY RESEARCH, v.45, no.10, pp.14910 - 14919
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF ENERGY RESEARCH
Volume
45
Number
10
Start Page
14910
End Page
14919
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/136951
DOI
10.1002/er.6767
ISSN
0363-907X
Abstract
Nanostructured transition metal chalcogenides (TMCs) have attracted attention as potential anode materials owing to the anticipation of next-generation battery systems, particularly potassium-ion batteries (PIBs). In this study, the electrochemical reaction mechanism of iron monosulfide (FeS) with potassium ions was systemically investigated for the first time. To enhance the electrochemical properties by improving the structural stability and electrical conductivity during cycling, rational strategies of introducing a yolk-shell architecture via an aerosol process and pitch solution infiltration were applied, resulting in the formation of yolk-shell-structured FeS/pitch-derived carbon composite microspheres (Y-FeS@C). From in situ and ex situ investigations of electrodes in fully discharged and charged states, the following reaction mechanism was determined from the second cycle onward: 4Fe + 4K(2)S <-> KxFe2S3 + FeS + Fe + (8 - x)K+ + (8 - x)e(-). The inhibition of substantial FeS crystal growth thanks to the pitch-derived carbon encapsulation as well as the formation of metallic Fe after the initial conversion reaction contributed to the excellent electrochemical kinetic properties of Y-FeS@C. Y-FeS@C showed stable cycle performance (256.5 mA h g(-1) for the 100th cycle at 0.5 A g(-1)) and high rate capability (113.8 mA h g(-1) at 5.0 A g(-1)) as an anode material for PIBs.
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