Decomposition of PVDF to delaminate cathode materials from end-of-life lithium-ion battery cathodes

The growing demand of electric vehicles and rapid consumption of rechargeable lithium-ion batteries (LIBs) require recycling of spent cathode active materials (CAMs) to reduce hazardous wastes and supply raw materials to LIB production. To separate CAMs from the cathode, direct calcination of polyvinylidene fluoride (PVDF) binder is widely applied, which leads to high energy consumption and release of toxic hydrogen fluoride. It is desirable to have an environmentally friendly and effective alternative to traditional direct calcination. In this study, five lithium salts, LiOAc (lithium acetate), LiNO3, LiCl, Li2CO3, and Li2SO4, were deployed and compared for their performance in recycling CAMs. A peel-off efficiency of up to 98.5% was achieved at a LiOAc to LiNO3 molar ratio of 3:2, salt to cathode mass ratio of 10:1, and temperature of 300 C at a holding time of 30 min. This system avoids corrosive chemicals and minimizes particle agglomeration of recycled products. Compared with sodium salt systems (NaOAc-NaNO3) or direct calcination, the LiOAc-LiNO3 system prevented high reaction temperature or further lithium loss, and minimized crystal structure and morphological changes. A decompo-sition mechanism of PVDF through adsorption of HF and fluorine substitution was proposed.

Automated summary

The increasing demand for electric vehicles and the rapid consumption of rechargeable lithium-ion batteries call for the recycling of spent cathode active materials (CAMs) to reduce hazardous wastes and provide raw materials for battery production. Traditional methods such as direct calcination of polyvinylidene fluoride (PVDF) binder have drawbacks of high energy consumption and toxic gas release. This study explores an environmentally friendly and effective alternative using different lithium salts, and achieves high peel-off efficiency with LiOAc and LiNO3. The mechanism of PVDF decomposition is proposed.