4.7 Article

Electrochemical-driven green recovery of lithium, graphite and cathode from lithium-ion batteries using water

期刊

WASTE MANAGEMENT
卷 150, 期 -, 页码 320-327

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.wasman.2022.07.026

关键词

Green recovery technology; Lithium extraction; Graphite recovery; Electrochemical lithium deposition

资金

  1. Department of Energy, Laboratory Directed Research and Development program at Ames National Laboratory
  2. U.S. Department of Energy by Iowa State University of Science and Technology [DE-AC02-07CH11358]

向作者/读者索取更多资源

This article introduces a process of lithium recovery using lithium plating, which allows for the extraction of metallic lithium at room temperature using water. Experimental results show a 37% improvement in lithium recovery rate with fast charging. This process also enables the recovery of high-purity graphite and transition metal oxides.
The expected exponential increase in consumption of lithium-ion batteries (LIBs) would pose a unique challenge to the availability of near-critical resources like lithium and graphite in the upcoming decade. We present a lithium recovery process that utilizes a degradation mechanism, i.e., lithium plating, as a tool to concentrate metallic lithium at the anode/separator interface for convenient extraction at room temperature - using only water. Electrochemical characterization of fast charged (1-6 C) LIBs yielded a maximum capacity fade of 50% over ten cycles. The lithium plating was confirmed via voltage plateau analysis, coulombic efficiency, and DC resistance measurements. A maximum lithium plating condition was observed to exist between 4C and 5C, thereby limiting the energy consumption in the extraction process. Post-mortem film thickness measurement showed an incrementing film deposition with a maximum of 35 mu m thickness. SEM and XPS analysis confirmed increasing concentration of a dense dendritic metallic lithium deposition on the anode/separator interface with C-rate. A green recovery process was adopted to extract the concentrated metallic lithium using distilled water. The lithium from the plated film, solid/electrolyte interface (SEI), electrolyte, anode, and cathode, was extracted as salts. A 37% improvement in lithium recoverability was achieved with fast charging under ambient conditions. XPS analysis showed-92% of lithium yield with no residual lithium in the graphite. In addition, the battery-grade graphite was recovered with 97% purity after heat treatment of the washed anode film, and concen-trated transition metals oxides in the cathode to 93% purity for convenient extraction.

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