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用于有机电极的贻贝启发型聚合物粘合剂

Mussel-Inspired Polymer Binders for Organic Electrodes.

作者信息

Battaglia Alicia M, Grignon Eloi, Liu Jiang Tian, Seferos Dwight S

机构信息

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada.

Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada.

出版信息

Small. 2024 Nov;20(47):e2405118. doi: 10.1002/smll.202405118. Epub 2024 Aug 14.

DOI:10.1002/smll.202405118
PMID:39140191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11579966/
Abstract

The development of polymer binders is necessary to meet the growing demands of modern energy storage technologies. While catechol-containing materials are proven successful in silicon anodes, their application in organic batteries remains unexplored. In this contribution, the synthesis of four polymers are described with nearly identical side chain composition but varying backbone structures. The materials are used to investigate the effect of polymer backbone structure on the binding abilities of catechol-containing materials. Comparative analysis with the commonly used polyvinylidene fluoride (PVDF) binder aims to address two critical questions: 1) Can catechol-rich polymers replace PVDF for use in organic cathodes? and 2) Does the choice of polymer backbone affect the performance of the battery?. The investigation reveals that supramolecular interactions, such as π-π stacking and coordination bonding, are pivotal features of catechol binders. Among the catechol-rich polymers, the polyacrylate binder stands out, likely attributed to its high flexibility. Additionally, introducing an oxygen atom into a catechol-rich polynorbornene enhances lithium-ion conductivity and rate performance. Overall, the findings highlight the viability of catechol-containing polymers as organic cathode binders, and that the choice of polymer backbone is a crucial factor for their use as lithium-ion battery binder materials.

摘要

聚合物粘结剂的发展对于满足现代储能技术不断增长的需求至关重要。虽然含儿茶酚的材料在硅阳极中已被证明是成功的,但其在有机电池中的应用仍未得到探索。在本论文中,描述了四种具有几乎相同侧链组成但主链结构不同的聚合物的合成。这些材料用于研究聚合物主链结构对含儿茶酚材料粘结能力的影响。与常用的聚偏氟乙烯(PVDF)粘结剂进行对比分析旨在解决两个关键问题:1)富含儿茶酚的聚合物能否替代PVDF用于有机阴极?2)聚合物主链的选择是否会影响电池性能?研究表明,超分子相互作用,如π-π堆积和配位键,是儿茶酚粘结剂的关键特性。在富含儿茶酚的聚合物中,聚丙烯酸酯粘结剂表现突出,这可能归因于其高柔韧性。此外,在富含儿茶酚的聚降冰片烯中引入氧原子可提高锂离子传导率和倍率性能。总体而言,研究结果突出了含儿茶酚聚合物作为有机阴极粘结剂的可行性,并且聚合物主链的选择是其作为锂离子电池粘结剂材料使用的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/c61d548fe22c/SMLL-20-2405118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/de563bca41b4/SMLL-20-2405118-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/100c6dfd06f9/SMLL-20-2405118-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/5c3ab393c2b0/SMLL-20-2405118-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/20a91c76a882/SMLL-20-2405118-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/ecc92b05912d/SMLL-20-2405118-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/ce45160bec76/SMLL-20-2405118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/c61d548fe22c/SMLL-20-2405118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/de563bca41b4/SMLL-20-2405118-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/100c6dfd06f9/SMLL-20-2405118-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/5c3ab393c2b0/SMLL-20-2405118-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/20a91c76a882/SMLL-20-2405118-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/ecc92b05912d/SMLL-20-2405118-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/ce45160bec76/SMLL-20-2405118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50f6/11579966/c61d548fe22c/SMLL-20-2405118-g002.jpg

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