Cathode refunctionalization as a lithium ion battery recycling alternative

被引:95
作者
Ganter, Matthew J. [1 ,2 ]
Landi, Brian J. [2 ,3 ]
Babbitt, Callie W. [1 ]
Anctil, Annick [4 ]
Gaustad, Gabrielle [1 ]
机构
[1] GIS, Rochester, NY 14623 USA
[2] NanoPower Res Labs NPRL, Rochester, NY 14623 USA
[3] Rochester Inst Technol, Rochester, NY 14623 USA
[4] Clemson Univ, Anderson, SC 29625 USA
基金
美国国家科学基金会;
关键词
Lithium ion batteries; Recycling; Sustainability; Waste management; End of life; GREENHOUSE-GAS EMISSIONS; PLUG-IN HYBRID; ENERGY-STORAGE; SECONDARY BATTERIES; RENEWABLE ENERGY; IMPACT;
D O I
10.1016/j.jpowsour.2014.01.078
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An approach to battery end-of-life (EOL) management is developed involving cathode refunctionalization, which enables remanufacturing of the cathode from EOL materials to regain the electrochemical performance. To date, the optimal end-of-life management of cathode materials is based on economic value and environmental impact which can influence the methods and stage of recycling. Traditional recycling methods can recover high value metal elements (e.g. Li, Co, Ni), but still require synthesis of new cathode from a mix of virgin and recovered materials. Lithium iron phosphate (LiFePO4) has been selected for study as a representative cathode material due to recent mass adoption and limited economic recycling drivers due to the low inherent cost of iron. Refunctionalization of EOL LiFePO4 cathode was demonstrated through electrochemical and chemical lithiation methods where the re-lithiated LiFePO4 regained the original capacity of 150-155 mAh g(-1). The environmental impact of the new recycling technique was determined by comparing the embodied energy of cathode material originating from virgin, recycled, and refunctionalized materials. The results demonstrate that the LiFePO4 refunctionalization process, through chemical lithiation, decreases the embodied energy by 50% compared to cathode production from virgin materials. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:274 / 280
页数:7
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