{"title":"An Electrochemical-Cycling-Induced Capacitive Component on the Surface of an Electrophoretic-Deposited Lithium Iron Phosphate Cathode","authors":"Byoung-Nam Park","doi":"10.3390/cryst14070658","DOIUrl":null,"url":null,"abstract":"In our research, we apply electrophoretic deposition (EPD) using AC voltage to investigate how high-C-rate electrochemical reactions affect pseudocapacitive charge storage in lithium iron phosphate (LFP) Li-ion batteries. This method significantly raises the battery’s specific capacity, achieving ~90 mAh/g at a 1 C-rate, along with outstanding cycle stability. Although we observe some capacity reduction over numerous cycles, there is a notable increase in the pseudocapacitive contribution to the battery’s charge storage. This is demonstrated by the consistent peak positions and currents during CV and a stable diffusion constant maintained at 9.6 × 10−9 cm2∙s−1. These findings highlight the battery’s durability, especially in high-demand scenarios. After an extended cycling period of ~500 cycles, the redox peaks related to the Fe2+/Fe3+ redox processes remain unchanged in terms of magnitude and position, indicating the battery’s excellent reversibility.","PeriodicalId":505131,"journal":{"name":"Crystals","volume":" 39","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystals","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/cryst14070658","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In our research, we apply electrophoretic deposition (EPD) using AC voltage to investigate how high-C-rate electrochemical reactions affect pseudocapacitive charge storage in lithium iron phosphate (LFP) Li-ion batteries. This method significantly raises the battery’s specific capacity, achieving ~90 mAh/g at a 1 C-rate, along with outstanding cycle stability. Although we observe some capacity reduction over numerous cycles, there is a notable increase in the pseudocapacitive contribution to the battery’s charge storage. This is demonstrated by the consistent peak positions and currents during CV and a stable diffusion constant maintained at 9.6 × 10−9 cm2∙s−1. These findings highlight the battery’s durability, especially in high-demand scenarios. After an extended cycling period of ~500 cycles, the redox peaks related to the Fe2+/Fe3+ redox processes remain unchanged in terms of magnitude and position, indicating the battery’s excellent reversibility.