Controllable hydrogen generation at low temperatures and safety evaluation for tin anode materials of spent lithium-ion batteries

被引:4
作者
Fan, Yue [1 ,2 ]
Zhang, Hongming [1 ,2 ]
Liu, Mili [1 ,2 ]
Zhang, Junrui [4 ]
Xiao, Xuezhang [3 ]
Ouyang, Liuzhang [1 ,2 ]
机构
[1] South China Univ Technol, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China
[2] South China Univ Technol, GuangDong Engn Technol Res Ctr Adv Energy Storage, Guangzhou 510641, Peoples R China
[3] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Peoples R China
[4] Lishui Univ, Dept Chem, Lishui 323000, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen generation; Hydrolysis; Safety; Li x Sn y alloys; Product recovery; THERMODYNAMIC ASSESSMENT; HYDROLYSIS; RECOVERY; STRATEGY; HYDRIDE; ENERGY;
D O I
10.1016/j.jallcom.2023.169548
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
Given the environmental pollution and thermal risks of lithium-ion batteries, it is necessary to recycle and evaluate the safety of spent lithium-ion batteries. Here, lithium tin alloys (LixSny) were prepared via mechanical alloying to simulate the tin anode materials at different lithium-embedded states. Among them, the Li22Sn5 alloy showed the optimum hydrolysis performance, releasing 351 mL g-1 hydrogen in 10 s at 293 K. The safety evaluation was carried out based on hydrolysis performance, maximum adiabatic temperature rise, and other parameters. The Li22Sn5 alloy required 738.8 mL of water to cool down to 303 K. Moreover, the reaction rates can be precisely controlled by tailoring the solution components, which effectively promoted the security and controllability for practical application. In addition, the hydrogen production of Li22Sn5 sample after hydrogenation increased to 624 mL g-1, even at a subzero temperature of 243 K, 510 mL g-1 hydrogen can be generated within 30 s. This study provides a new idea for the safety evaluation and recycling of tin anode materials in spent lithium-ion batteries. (c) 2023 Elsevier B.V. All rights reserved.
引用
收藏
页数:11
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