优化单向堆叠磷酸铁锂正极中的 Li+ 离子扩散途径:增强电化学性能和长期稳定性

IF 13.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Chemical Engineering Journal Pub Date : 2024-11-19 DOI:10.1016/j.cej.2024.157788
Sujeong Kim, Jemin Lee, Hojun Moon, Jaehun Lee, Hyunsub Shin, Jun Sung Lee, Sang Woo Joo, Jeeyoung Yoo, Misook Kang
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引用次数: 0

摘要

在本研究中,我们介绍了一种创新方法,通过新型糖辅助单向堆积法提高磷酸铁锂(LiFePO4,LFP)正极材料的电化学性能和使用寿命。磷酸铁锂固有的挑战,如低锂离子扩散性和有限的导电性,通过利用糖类作为粘合剂来实现磷酸铁锂颗粒的精确排列得到了解决。这种方法有助于形成畅通无阻的锂离子通路,显著提高锂离子扩散率和循环稳定性。未经改性的 LFP 阴极的锂离子扩散系数(DLi+)为 7.79 × 10-12 cm2 s-1,而 S5(蔗糖 5%)LFP 阴极的扩散系数则高达 3.5 × 10-10 cm2 s-1。此外,在 0.1C 放电速率下,S5-LFP 的放电容量高达 165.1 mAh g-1,而未改性 LFP 的放电容量仅为 147.8 mAh g-1。循环稳定性也有明显提高,S5-LFP 在 5C 速率下循环 2,000 次后,容量保持率为 86.3%,而未经改性的 LFP 在相同条件下容量保持率仅为 79.2%。这些改进归功于通过糖辅助堆叠实现的优化粒子排列,从而增强了 Li+ 离子的扩散和整体电化学性能。此外,S5-LFP 阴极的结构完整性和电化学稳定性还通过一套全面的表征方法和电化学测试得到了彻底验证,凸显了该技术在电池制造方面的可扩展性和成本效益。阴极材料设计方面的这一突破为开发高性能、耐用的锂离子电池,尤其是应用于电动汽车和其他要求苛刻的储能系统提供了一条前景广阔的途径。
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Optimized Li+ ion diffusion pathways in unidirectional stacked lithium iron phosphate cathodes: Enhanced electrochemical performance and long-term stability
In this study, we introduce an innovative approach to enhance the electrochemical performance and longevity of lithium iron phosphate (LiFePO4, LFP) cathode materials through a novel saccharide-assisted unidirectional stacking method. The inherent challenges of LFP, such as low lithium-ion diffusion and limited electrical conductivity, are addressed by leveraging saccharides as binders to achieve precise alignment of LFP particles. This method facilitates the formation of unobstructed lithium-ion pathways, significantly enhancing Li+ ion diffusion rates and cycle stability. The unmodified LFP cathode exhibited a lithium-ion diffusion coefficient (DLi+) of 7.79 × 10−12 cm2 s−1, while the S5 (sucrose 5 %) LFP cathode demonstrated a superior diffusion coefficient of 3.5 × 10−10 cm2 s−1. Additionally, the S5-LFP achieved a remarkable discharge capacity of 165.1 mAh g−1 at a 0.1C rate, compared to 147.8 mAh g−1 for the unmodified LFP. The cycle stability was also significantly improved, with the S5-LFP retaining 86.3 % of its capacity after 2,000 cycles at a 5C rate, whereas the unmodified LFP retained only 79.2 % under the same conditions. These improvements are attributed to the optimized particle alignment achieved through saccharide-assisted stacking, which enhances Li+ ion diffusion and overall electrochemical performance. Additionally, the structural integrity and electrochemical stability of the S5-LFP cathodes were thoroughly validated through a comprehensive set of characterization methods and electrochemical tests, highlighting the scalability and cost-effectiveness of this technique for battery manufacturing. This breakthrough in cathode material design offers a promising pathway for the development of high-performance, durable lithium-ion batteries, particularly for applications in electric vehicles and other demanding energy storage systems.
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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