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在深共熔氯化胆碱+尿素溶剂中从锂钴氧化物中电化学回收钴

Cobalt Electrochemical Recovery from Lithium Cobalt Oxides in Deep Eutectic Choline Chloride+Urea Solvents.

作者信息

Wang Hongmin, Li Mengran, Garg Sahil, Wu Yuming, Nazmi Idros Mohamed, Hocking Rosalie, Duan Haoran, Gao Shuai, Yago Anya Josefa, Zhuang Linzhou, Rufford Thomas Edward

机构信息

School of Chemical Engineering, The University of Queensland, St Lucia, 4072, Brisbane, Australia.

Department of Chemistry and Biotechnology, Centre for Translational Atomaterials and ARC Training Centre for Surface Engineering for Advanced Materials, SEAM, Swinburne University of Technology, Hawthorn, 3122, Melbourne, VIC, Australia.

出版信息

ChemSusChem. 2021 Jul 22;14(14):2972-2983. doi: 10.1002/cssc.202100954. Epub 2021 Jun 18.

Abstract

Electrochemical recovery of the cobalt in deep eutectic solvent shows its promise in recycling and recovery of valuable elements from the spent lithium-ion battery due to its high selectivity and minimal environmental impacts. This work unveiled the roles of the substrates, applied potentials, and operating temperatures on the performance of cobalt electrochemical recovery in a deep eutectic choline chloride+urea solvent. The solvent contains cobalt and lithium ions extracted from lithium cobalt oxides - 3an essential lithium-ion battery cathode material. Our results highlight that the substrate predetermines the cobalt recovery modes via substrate-cobalt interactions, which could be predicted by the cobalt surface segregation energies and crystallographic misfits. We also show that a moderate cathode potential under -1.0 V vs. silver quasi-reference electrode at 94-104 °C is essential to ensure a selective cobalt recovery at an optimal rate. We also found that the stainless-steel mesh is an optimal substrate for cobalt recovery due to its relatively high selectivity, fast recovery rate, and easy cobalt collection. Our work provides new insights on metal recovery in deep eutectic solvents and offers a new avenue to control the metal electrodeposition modes via modulation of substrate compositions and crystal structures.

摘要

在深共晶溶剂中对钴进行电化学回收,因其具有高选择性和最小的环境影响,在从废旧锂离子电池中回收和再利用有价值元素方面展现出了前景。这项工作揭示了底物、施加电位和操作温度对在深共晶氯化胆碱+尿素溶剂中钴电化学回收性能的影响。该溶剂含有从锂钴氧化物(一种重要的锂离子电池阴极材料)中提取的钴和锂离子。我们的结果表明,底物通过底物-钴相互作用预先决定了钴的回收模式,这可以通过钴的表面偏析能和晶体学失配来预测。我们还表明,在94-104°C下相对于银准参比电极施加-1.0 V的适度阴极电位对于以最佳速率确保选择性钴回收至关重要。我们还发现,不锈钢网是钴回收的最佳底物,因为它具有相对较高的选择性、快速的回收率和易于收集钴的特点。我们的工作为深共晶溶剂中的金属回收提供了新的见解,并通过调节底物组成和晶体结构为控制金属电沉积模式提供了一条新途径。

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