从废锂离子电池工艺浸出液中可持续地回收双功能电活性材料

Satyaswini Sahu, Arya Das, Sushree Pattnaik, Ayan Mukherjee, Suddhasatwa Basu and Mamata Mohapatra*, 
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引用次数: 0

摘要

本研究对富镍钴草酸盐(rMOx)和氧化物(rMO)进行了比较分析,这两种材料是从废旧锂离子电池(LIB)的浸出液中采用经济环保的策略开发出来的,可作为超级电容器和碱性介质中氧进化反应(OER)应用的电活性材料。利用串联方法,从废锂电池浸出液中回收了 rMOx 和 rMO,过渡金属离子的回收率达到 90%。在 1 Ag-1 的条件下,rMOx 的放电比电容为 220 Fg-1,超过了 rMO 的 156.5 Fg-1。为了分析 rMOx 和 MXene 的实际应用性,我们制作了一个非对称超级电容器装置,在 0.8 mA cm-2 的条件下,放电比电容达到 46 Fg-1,能量密度和功率密度分别为 6.43 Wh kg-1 和 303.03 W kg-1。就 OER 而言,rMOx 在 10 mA cm-2 时的过电位为 176 mV,Tafel 斜坡为 81 mV dec-1,表现优于 rMO 和基准电催化剂 IrO2。rMOx 的优异性能可归因于其在电极-电解质相互作用过程中由金属-草酸盐转化为金属-氧化物-氢氧化物所形成的更高的电化学活性中心。因此,本研究提出了一种建立电化学双功能性和能源可持续性的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sustainable Recovery of Bifunctional Electroactive Material from Process Leach Liquor of Spent Lithium-Ion Battery

Sustainable Recovery of Bifunctional Electroactive Material from Process Leach Liquor of Spent Lithium-Ion Battery

This study presents a comparative analysis of Ni-Co rich oxalate (rMOx) and oxide (rMO), developed from process leach liquor of spent lithium-ion batteries (LIBs) following an economic and environmentally friendly strategy, as an electroactive material for supercapacitor and the oxygen evolution reaction (OER) applications in alkaline media. Utilizing a tandem approach, rMOx and rMO were recovered from spent LIBs leach liquor, achieving >90% recovery of transition metal ions. rMOx shows a discharge specific capacitance of 220 Fg–1 at 1 Ag–1, surpassing the rMO of 156.5 Fg–1. An asymmetric supercapacitor device fabricated to analyze the practical applicability using rMOx and MXene achieved a discharge specific capacitance of 46 Fg–1 at 0.8 mA cm–2 with energy and power densities of 6.43 Wh kg–1 and 303.03 W kg–1, respectively. In the case of OER, rMOx exhibited an overpotential of 176 mV at 10 mA cm–2 and a Tafel slope of 81 mV dec–1, outperforming rMO and benchmark electrocatalyst IrO2. The superior performance of rMOx can be attributed to its higher electrochemical active center formation due to metal-oxalate to metal-oxy-hydroxide conversion during electrode-electrolyte interaction. Thus, this study presents a novel approach for establishing electrochemical bifunctionality and energy sustainability.

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