A. T. Nguyen, V. Phung, V. Mittova, H. Ngo, Thuan Ngoc Vo, My Linh Le Thi, V. Nguyen, I. Mittova, M. Le, Y. Ahn, I. Kim, Tuan Loi Nguyen
{"title":"Fabricating Nanostructured HoFeO 3 Perovskite for Lithium-Ion Battery Anodes via Co-Precipitation","authors":"A. T. Nguyen, V. Phung, V. Mittova, H. Ngo, Thuan Ngoc Vo, My Linh Le Thi, V. Nguyen, I. Mittova, M. Le, Y. Ahn, I. Kim, Tuan Loi Nguyen","doi":"10.2139/ssrn.3882746","DOIUrl":null,"url":null,"abstract":"Nanostructured HoFeO3 perovskite was successfully prepared via co-precipitation of Fe3+ and Ho3+ ions in ethanol, followed by heat treatment. Analysis revealed the orthorhombic structure, uniaxial orientation, and nanograin size. This anode material exhibited excellent electrochemical properties in lithium-ion batteries including high capacity retention and Coulombic efficiency, good cyclability, low charge transfer, high Li+ diffusion coefficient, and excellent rate performance. They delivered reversible capacity of 437 mAh g-1 after 120 cycles at current density of 0.1 A g-1, a charge capacity of 299 mAh g-1 even at high current density of 10 A g-1. Outstanding performance can be ascribed to unique nanostructured perovskite. Nanosized materials offer a larger electrode/electrolyte interface, and reduce Li-ion diffusion length, improving reaction kinetics. Perovskite structure effectively prevented anode degradation during cycling, demonstrating excellent reversible storage. Kinetics of electrochemical reactions were also studied. All indicate the great potential of HoFeO3 perovskite as an anode material in LIBs.","PeriodicalId":412570,"journal":{"name":"Electrochemistry eJournal","volume":"57 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry eJournal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2139/ssrn.3882746","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
Abstract
Nanostructured HoFeO3 perovskite was successfully prepared via co-precipitation of Fe3+ and Ho3+ ions in ethanol, followed by heat treatment. Analysis revealed the orthorhombic structure, uniaxial orientation, and nanograin size. This anode material exhibited excellent electrochemical properties in lithium-ion batteries including high capacity retention and Coulombic efficiency, good cyclability, low charge transfer, high Li+ diffusion coefficient, and excellent rate performance. They delivered reversible capacity of 437 mAh g-1 after 120 cycles at current density of 0.1 A g-1, a charge capacity of 299 mAh g-1 even at high current density of 10 A g-1. Outstanding performance can be ascribed to unique nanostructured perovskite. Nanosized materials offer a larger electrode/electrolyte interface, and reduce Li-ion diffusion length, improving reaction kinetics. Perovskite structure effectively prevented anode degradation during cycling, demonstrating excellent reversible storage. Kinetics of electrochemical reactions were also studied. All indicate the great potential of HoFeO3 perovskite as an anode material in LIBs.
将Fe3+和Ho3+离子在乙醇中共沉淀,然后进行热处理,成功制备了纳米HoFeO3钙钛矿。分析表明,该材料具有正交结构、单轴取向和纳米晶粒尺寸。该负极材料在锂离子电池中具有良好的电化学性能,包括高容量保持率和库仑效率、良好的可循环性、低电荷转移率、高Li+扩散系数和优异的倍率性能。在0.1 A g-1的电流密度下,经过120次循环后,它们的可逆容量为437 mAh g-1,即使在10 A g-1的高电流密度下,充电容量也达到299 mAh g-1。优异的性能可归因于独特的纳米结构钙钛矿。纳米材料提供了更大的电极/电解质界面,减少了锂离子的扩散长度,改善了反应动力学。钙钛矿结构有效地防止了循环过程中阳极的降解,表现出优异的可逆存储。对电化学反应动力学进行了研究。这些都表明了HoFeO3钙钛矿作为锂离子电池负极材料的巨大潜力。