How Binder Nanofibration Affects the Active‐Material Microenvironment in Battery Electrodes?

材料科学 电极 电解质 压延 复合材料 电池(电) 毛细管作用 微观结构 弯曲 灵活性(工程) 润湿 纳米技术 物理化学 化学 功率(物理) 物理 统计 量子力学 数学
作者
Cheng‐Ye Ma,Wenrui Cai,Zhiwei Zhu,Zhongfeng Ji,Jiarui Yang,Hua Li,Guojiang Wen,Zhiyu Zhao,Xuewei Fu,Wei Yang,Yu Wang
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:35 (2) 被引量:14
标识
DOI:10.1002/adfm.202412193
摘要

Abstract Binder morphology is a critical factor determining the electrode microstructures and properties, which fundamentally controls the charge transport and mechanical performance of the resultant battery. In this case, polytetrafluoroethylene (PTFE) binder is of great interest as it exhibits unique nanofibration capability and mechanical flexibility, which has been broadly applied for dry processing of battery electrodes. However, there is a lack of fundamental study on how binder nanofibration affects the electrochemomechanical properties of electrodes. Here, similar to the fibrous structures of the cell microenvironment, the attempt is to answer this question from the viewpoint of active‐material microenvironment (ME@AM). First, the PTFE nanofibration degree is adjusted by electrode calendering treatment and binder loading. Second, the microstructures, mechanical relaxation behavior, bending capability, and liquid–electrolyte wetting capability of the fibrous ME@AM are comparatively investigated in detail by dynamic mechanical testing. Finally, the superiority of highly fibrous ME@AM in electrochemical performance is confirmed by the C‐rate and cycling stability testing of half‐cells. This study indicates that a highly fibrous ME@AM can remarkably improve the electrochemomechanical properties of electrodes by enhanced capillary action with liquid electrolyte, good electrode flexibility, and structural stability under compression.
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