Optimizing Carbon Coating Process for Lithium-Rich LiFePO4 Cathode Materials.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY ChemSusChem Pub Date : 2025-03-21 DOI:10.1002/cssc.202402558
Shin Park, Docheon Ahn, Jihee Yoon, Changshin Jo
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引用次数: 0

Abstract

Li1+xFe1-xPO4 (Li-rich LFP) has been proposed as an alternative to address low ionic and electronic conductivity of stoichiometric LiFePO4 (LFP). However, comprehensive studies investigating the impact of the carbon coating process on crystal structure and electrochemical performance during the synthesis of Li-rich LFP are still lacking. In particular, the characteristics of carbon precursor and calcination atmosphere significantly influence formation of crystal structure and electrochemical properties of the Li-rich LFP, underlining the necessity for further investigation. In this study, we compare two synthesis process: introducing carbon precursor before formation of LFP crystal structure (C/BLF) and adding it an additional calcination step after structure has formed (C/ALF). The C/ALF process sample has a larger unit cell volume and denser coating layer. As a result, the C/ALF sample exhibits a lower overpotential (0.54 V) and a higher discharge capacity (~134.13 mAhg-1) than C/BLF sample. These findings elucidate the influence of carbon coating process sequence on crystal structure and electrochemical performance during the synthesis of Li-rich LFP.

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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
期刊最新文献
Optimizing Carbon Coating Process for Lithium-Rich LiFePO4 Cathode Materials. A review of CO2 hydrogenation to liquid fuels. Enzymatic Cleanup of Formaldehyde in Aqueous Solutions. Heterogeneous photocatalytic systems formed by compound [Zr6O4(OH)4(C6H5COO)8(H2O)8][SiW12O40] in combination with inorganic cocatalysts for CO2 reduction to alcohols in water. Perspectives and limitations of tartaric acid diamides as phase change materials for sustainable heat applications.
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