{"title":"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","authors":"Satyaswini Sahu, Arya Das, Sushree Pattnaik, Ayan Mukherjee, Suddhasatwa Basu and Mamata Mohapatra*, ","doi":"10.1021/acssusresmgt.4c0021510.1021/acssusresmgt.4c00215","DOIUrl":null,"url":null,"abstract":"<p >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<sup>–1</sup> at 1 Ag<sup>–1</sup>, surpassing the rMO of 156.5 Fg<sup>–1</sup>. An asymmetric supercapacitor device fabricated to analyze the practical applicability using rMOx and MXene achieved a discharge specific capacitance of 46 Fg<sup>–1</sup> at 0.8 mA cm<sup>–2</sup> with energy and power densities of 6.43 Wh kg<sup>–1</sup> and 303.03 W kg<sup>–1</sup>, respectively. In the case of OER, rMOx exhibited an overpotential of 176 mV at 10 mA cm<sup>–2</sup> and a Tafel slope of 81 mV dec<sup>–1</sup>, outperforming rMO and benchmark electrocatalyst IrO<sub>2</sub>. 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.</p>","PeriodicalId":100015,"journal":{"name":"ACS Sustainable Resource Management","volume":"1 9","pages":"2119–2127 2119–2127"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sustainable Recovery of Bifunctional Electroactive Material from Process Leach Liquor of Spent Lithium-Ion Battery\",\"authors\":\"Satyaswini Sahu, Arya Das, Sushree Pattnaik, Ayan Mukherjee, Suddhasatwa Basu and Mamata Mohapatra*, \",\"doi\":\"10.1021/acssusresmgt.4c0021510.1021/acssusresmgt.4c00215\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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<sup>–1</sup> at 1 Ag<sup>–1</sup>, surpassing the rMO of 156.5 Fg<sup>–1</sup>. An asymmetric supercapacitor device fabricated to analyze the practical applicability using rMOx and MXene achieved a discharge specific capacitance of 46 Fg<sup>–1</sup> at 0.8 mA cm<sup>–2</sup> with energy and power densities of 6.43 Wh kg<sup>–1</sup> and 303.03 W kg<sup>–1</sup>, respectively. In the case of OER, rMOx exhibited an overpotential of 176 mV at 10 mA cm<sup>–2</sup> and a Tafel slope of 81 mV dec<sup>–1</sup>, outperforming rMO and benchmark electrocatalyst IrO<sub>2</sub>. 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.</p>\",\"PeriodicalId\":100015,\"journal\":{\"name\":\"ACS Sustainable Resource Management\",\"volume\":\"1 9\",\"pages\":\"2119–2127 2119–2127\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Sustainable Resource Management\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acssusresmgt.4c00215\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sustainable Resource Management","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssusresmgt.4c00215","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.