Jonathan Højberg, Kristian B. Knudsen, J. Hjelm, T. Vegge
{"title":"锂氧电池充电过程中的反应和SEI形成","authors":"Jonathan Højberg, Kristian B. Knudsen, J. Hjelm, T. Vegge","doi":"10.1149/2.0051507EEL","DOIUrl":null,"url":null,"abstract":"Reactions and SEI Formation during Charging of Li-O2 Cells In this letter we combine detailed electrochemical impedance measurements with quantitative measurements of O2 evolution and Li2O2 oxidation to describe the charge mechanisms during charge of Li-O2 batteries with porous carbon electrodes. We identify Li2O2 oxidation at 3.05 V and an apparent chemical formation of a solid electrolyte interface (SEI) layer as the first monolayer of Li2O2 is oxidized, leading to a voltage increase. The first electrochemical degradation reaction is identified between 3.3 V and 3.5 V, and the chemical degradation is limited above 3.5 V, suggesting that a chemically stable SEI layer has been formed.","PeriodicalId":11470,"journal":{"name":"ECS Electrochemistry Letters","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1149/2.0051507EEL","citationCount":"11","resultStr":"{\"title\":\"Reactions and SEI Formation during Charging of Li-O2 Cells\",\"authors\":\"Jonathan Højberg, Kristian B. Knudsen, J. Hjelm, T. Vegge\",\"doi\":\"10.1149/2.0051507EEL\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Reactions and SEI Formation during Charging of Li-O2 Cells In this letter we combine detailed electrochemical impedance measurements with quantitative measurements of O2 evolution and Li2O2 oxidation to describe the charge mechanisms during charge of Li-O2 batteries with porous carbon electrodes. We identify Li2O2 oxidation at 3.05 V and an apparent chemical formation of a solid electrolyte interface (SEI) layer as the first monolayer of Li2O2 is oxidized, leading to a voltage increase. The first electrochemical degradation reaction is identified between 3.3 V and 3.5 V, and the chemical degradation is limited above 3.5 V, suggesting that a chemically stable SEI layer has been formed.\",\"PeriodicalId\":11470,\"journal\":{\"name\":\"ECS Electrochemistry Letters\",\"volume\":\"4 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1149/2.0051507EEL\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ECS Electrochemistry Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1149/2.0051507EEL\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Electrochemistry Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/2.0051507EEL","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11
摘要
在这篇文章中,我们将详细的电化学阻抗测量与O2演化和Li2O2氧化的定量测量相结合,描述了多孔碳电极Li-O2电池充电过程中的充电机制。我们发现Li2O2在3.05 V时氧化,并且随着第一层Li2O2被氧化,导致电压升高,固体电解质界面(SEI)层的明显化学形成。在3.3 V ~ 3.5 V之间发生了第一次电化学降解反应,在3.5 V以上发生的化学降解受到限制,表明已经形成了化学稳定的SEI层。
Reactions and SEI Formation during Charging of Li-O2 Cells
Reactions and SEI Formation during Charging of Li-O2 Cells In this letter we combine detailed electrochemical impedance measurements with quantitative measurements of O2 evolution and Li2O2 oxidation to describe the charge mechanisms during charge of Li-O2 batteries with porous carbon electrodes. We identify Li2O2 oxidation at 3.05 V and an apparent chemical formation of a solid electrolyte interface (SEI) layer as the first monolayer of Li2O2 is oxidized, leading to a voltage increase. The first electrochemical degradation reaction is identified between 3.3 V and 3.5 V, and the chemical degradation is limited above 3.5 V, suggesting that a chemically stable SEI layer has been formed.