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一种赋予磷酸铁锂电极结构完整性和长循环寿命性能的环保型交联粘结剂。

An environment-friendly crosslinked binder endowing LiFePO electrode with structural integrity and long cycle life performance.

作者信息

Zhao Lingzhu, Sun Zhipeng, Zhang Hongbing, Li Yuli, Mo Yan, Yu Feng, Chen Yong

机构信息

State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan Provincial Key Laboratory of Research on Utilization of Si-Zr-Ti Resources, College of Materials Science and Engineering, Hainan University Renmin Road No. 58 Haikou 570228 PR China

Institution of Plastic Surgery, Weifang Medical University Weifang 261042 P. R. China.

出版信息

RSC Adv. 2020 Aug 11;10(49):29362-29372. doi: 10.1039/d0ra05095d. eCollection 2020 Aug 5.

Abstract

Lithium iron phosphate (LiFePO) is one of the most widely used cathode materials of lithium ion batteries. However, its commercial binder polyvinylidene fluoride (PVDF) is costly, less environmental-friendly and unstable during the long cycling process because of the weak van der Waals forces between the PVDF binder and electrode materials. Herein, an aqueous binder was designed using methacrylate-modified gelatin through UV photo-crosslinking. The crosslinked network and specific functional groups (carboxyl and amino) of the gelatin binder are superior in stabilizing the LiFePO electrode structure during long cycles by mitigating the formation of cracks and suppressing the detachment of electrode materials from the Al current collector. The LiFePO electrode with gelatin binder displays a high capacity of 140.3 mA h g with 90.1% retention after 300 cycles at 0.5C, which are both superior to that of the PVDF binder (only 114.4 mA h g and 74.8%). This work provides a promising binder to replace the commercial PVDF binder for practical application in energy storage systems.

摘要

磷酸铁锂(LiFePO)是锂离子电池中应用最广泛的正极材料之一。然而,其商业粘合剂聚偏氟乙烯(PVDF)成本高昂,环保性较差,并且由于PVDF粘合剂与电极材料之间的范德华力较弱,在长循环过程中不稳定。在此,通过紫外光交联设计了一种使用甲基丙烯酸酯改性明胶的水性粘合剂。明胶粘合剂的交联网络和特定官能团(羧基和氨基)通过减轻裂纹的形成和抑制电极材料与铝集流体的分离,在长循环过程中稳定LiFePO电极结构方面表现出色。具有明胶粘合剂的LiFePO电极在0.5C下300次循环后显示出140.3 mA h g的高容量,保留率为90.1%,两者均优于PVDF粘合剂(仅为114.4 mA h g和74.8%)。这项工作为储能系统的实际应用提供了一种有前景的粘合剂来替代商业PVDF粘合剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfc2/9055956/bfc6ca134626/d0ra05095d-f1.jpg

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