Volume 135, Issue 14 46132
Article

Water-soluble binder PAALi with terpene resin emulsion as tackifier for LiFePO4 cathode

Jiarong He

Jiarong He

Key Laboratory of Renewable Energy, Guangdong Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, No. 2, Nengyuan Road, Guangzhou, Guangdong 510640, China

University of Chinese Academy of Sciences, Beijing, 100049 China

Search for more papers by this author
Haoxiang Zhong

Haoxiang Zhong

Key Laboratory of Renewable Energy, Guangdong Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, No. 2, Nengyuan Road, Guangzhou, Guangdong 510640, China

Search for more papers by this author
Lingzhi Zhang

Corresponding Author

Lingzhi Zhang

Key Laboratory of Renewable Energy, Guangdong Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, No. 2, Nengyuan Road, Guangzhou, Guangdong 510640, China

Correspondence to: L. Zhang (E-mail: [email protected])Search for more papers by this author
First published: 12 December 2017
Citations: 22

ABSTRACT

Terpene resin (TS) emulsion has been adopted as a tackifier in lithium polyacrylate (PAALi) as water-soluble binder for LiFePO4 (LFP) cathode in Li-ion batteries. TS–PAALi composite binder with optimal ratio of 1:1 (denoted as TS1–PAALi1), shows improved flexibility and enhanced adhesion capability of 0.170 N/cm in comparison with 0.120 N/cm of PAALi after introducing TS as adhesion enhancing agent, which is comparable with that of nonaqueous poly(vinylidene difluoride) (PVDF, 0.171 N/cm) and much better than aqueous sodium carboxymethyl cellulose (CMC, 0.045 N/cm). The electrochemical characteristics of LFP with TS1–PAALi1 have been investigated and further compared with those of PAALi, CMC, and PVDF. LFP with TS1–PAALi1 exhibits superior cycling stability and rate capability, maintaining 65.57% capacity of 0.2 C at 5 C rate in comparison with 60.73%, 57.83%, and 34.79% for PAALi, CMC, and PVDF, respectively. In addition, LFP with TS1–PAALi1 displays excellent cycling performance almost without any capacity fading at 60 °C after 45 cycles at 1 C, much better than that of PAALi, CMC, and PVDF. Cyclic voltammetry and electrochemical impedance spectroscopy reveal that LFP with TS1–PAALi1 has a smaller redox potential difference, lower electrode polarization, and a more favorable electrochemical kinetics (fast lithium diffusion rate) than that of PAALi, CMC, and PVDF, thus more superior electrochemical performances. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46132.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.