Modulating electrolyte solvation structures with Fe-embedded carbon matrix substrates for robust lithium-metal plating

The practical application of lithium metal as an anode faces challenges due to the uncontrolled growth of lithium dendrites and substantial volume expansion. In this study, we synthesized a porous Fe@C material through the pyrolysis of Fe-based metal-organic frameworks (MOFs), showcasing its efficac...

Full description

Saved in:
Bibliographic Details
Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 13; no. 2; pp. 928 - 932
Main Authors Peng, Jiayue, Wang, Jinghan, Pu, Xiangjun, Xie, Jia
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 02.01.2025
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The practical application of lithium metal as an anode faces challenges due to the uncontrolled growth of lithium dendrites and substantial volume expansion. In this study, we synthesized a porous Fe@C material through the pyrolysis of Fe-based metal-organic frameworks (MOFs), showcasing its efficacy as a substrate for lithium plating. Increased anion participation occurs in the Li + solvation sheath within the Fe@C pores, leading to the formation of an anion-derived solid electrolyte interface (SEI). The Fe matrix serves as nucleation sites, and the pores optimize the electrolyte structure, effectively guiding Li deposition while inhibiting Li dendrite formation. This approach demonstrates outstanding electrochemical performance with extended cycling, presenting a promising strategy for stable lithium metal anodes. Carbonized Fe-BTC to Fe@C is utilized as a substrate to enhance lithium deposition by modulating the Li + solvation structure. This approach significantly improves cycling performance.
Bibliography:Electronic supplementary information (ESI) available. See DOI
https://doi.org/10.1039/d4ta07545e
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:2050-7488
2050-7496
DOI:10.1039/d4ta07545e