{"title":"用于快速锂离子存储的垂直排列MXene电极的尺寸依赖性电化学性能","authors":"Sho Hideshima , Yusuke Kawasaki , Daisuke Takimoto , Yury Gogotsi , Wataru Sugimoto","doi":"10.1016/j.electacta.2025.145849","DOIUrl":null,"url":null,"abstract":"<div><div>MXenes are attractive electrode materials for batteries and pseudocapacitors because they have higher electronic conductivity than carbons or oxides and can exhibit surface-confined redox reactions. However, restacking of 2D nanosheets may limit the ionic transport in MXene electrodes and lead to sluggish charge/discharge. To understand and control the 2D mass transport properties of Ti<sub>3</sub>C<sub>2</sub>T<em><sub>x</sub></em> MXene, we fabricated electrodes with different diffusion lengths and nanosheet alignments (vertical and horizontal). The electrodes were made by combining electrophoretic deposition and freeze-drying of delaminated size-regulated MXenes (95 to ∼600 nm lateral size). Their electrochemical lithiation/de-lithiation behavior was studied in a non-aqueous electrolyte. Vertically-aligned Ti<sub>3</sub>C<sub>2</sub>T<em><sub>x</sub></em> MXene film with a thickness of 300 μm provided faster Li<sup>+</sup> storage than horizontally-stacked MXene film with a thickness of 10 μm. Electrodes made of small-size flakes exhibited higher discharge capacity and capacity retention at high rates due to a shorter Li<sup>+</sup> diffusion path. The vertically aligned MXene electrodes show high electrochemical performance and fast charge/discharge.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"519 ","pages":"Article 145849"},"PeriodicalIF":5.6000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Size-dependent electrochemical properties of vertically aligned MXene electrodes for fast Li-ion storage\",\"authors\":\"Sho Hideshima , Yusuke Kawasaki , Daisuke Takimoto , Yury Gogotsi , Wataru Sugimoto\",\"doi\":\"10.1016/j.electacta.2025.145849\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>MXenes are attractive electrode materials for batteries and pseudocapacitors because they have higher electronic conductivity than carbons or oxides and can exhibit surface-confined redox reactions. However, restacking of 2D nanosheets may limit the ionic transport in MXene electrodes and lead to sluggish charge/discharge. To understand and control the 2D mass transport properties of Ti<sub>3</sub>C<sub>2</sub>T<em><sub>x</sub></em> MXene, we fabricated electrodes with different diffusion lengths and nanosheet alignments (vertical and horizontal). The electrodes were made by combining electrophoretic deposition and freeze-drying of delaminated size-regulated MXenes (95 to ∼600 nm lateral size). Their electrochemical lithiation/de-lithiation behavior was studied in a non-aqueous electrolyte. Vertically-aligned Ti<sub>3</sub>C<sub>2</sub>T<em><sub>x</sub></em> MXene film with a thickness of 300 μm provided faster Li<sup>+</sup> storage than horizontally-stacked MXene film with a thickness of 10 μm. Electrodes made of small-size flakes exhibited higher discharge capacity and capacity retention at high rates due to a shorter Li<sup>+</sup> diffusion path. The vertically aligned MXene electrodes show high electrochemical performance and fast charge/discharge.</div></div>\",\"PeriodicalId\":305,\"journal\":{\"name\":\"Electrochimica Acta\",\"volume\":\"519 \",\"pages\":\"Article 145849\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-02-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electrochimica Acta\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0013468625002129\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468625002129","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
Size-dependent electrochemical properties of vertically aligned MXene electrodes for fast Li-ion storage
MXenes are attractive electrode materials for batteries and pseudocapacitors because they have higher electronic conductivity than carbons or oxides and can exhibit surface-confined redox reactions. However, restacking of 2D nanosheets may limit the ionic transport in MXene electrodes and lead to sluggish charge/discharge. To understand and control the 2D mass transport properties of Ti3C2Tx MXene, we fabricated electrodes with different diffusion lengths and nanosheet alignments (vertical and horizontal). The electrodes were made by combining electrophoretic deposition and freeze-drying of delaminated size-regulated MXenes (95 to ∼600 nm lateral size). Their electrochemical lithiation/de-lithiation behavior was studied in a non-aqueous electrolyte. Vertically-aligned Ti3C2Tx MXene film with a thickness of 300 μm provided faster Li+ storage than horizontally-stacked MXene film with a thickness of 10 μm. Electrodes made of small-size flakes exhibited higher discharge capacity and capacity retention at high rates due to a shorter Li+ diffusion path. The vertically aligned MXene electrodes show high electrochemical performance and fast charge/discharge.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.