Baosong Li , Dezhuang Ji , Abdallah Kamal Hamouda , Shaohong Luo
{"title":"MXene-derived TiO2 nanosheets/rGO heterostructures for superior sodium-ion storage","authors":"Baosong Li , Dezhuang Ji , Abdallah Kamal Hamouda , Shaohong Luo","doi":"10.1016/j.chphma.2024.05.001","DOIUrl":null,"url":null,"abstract":"<div><div>Transition metal oxides hold promise as electrode materials for energy-storage devices such as batteries and supercapacitors. However, achieving ideal electrode materials with high capacity, long-term cycling stability, and superb rate capability remains a challenge. In this study, we present a self-assembled heterogeneous structure consisting of TiO<sub>2</sub> nanosheets derived from Ti<sub>3</sub>C<sub>2</sub>T<em><sub>x</sub></em> MXene and reduced graphene oxide. This structure facilitates the formation of heterogeneous structures while establishing a conductive network. The restacking of porous TiO<sub>2</sub> nanosheets and reduced graphene oxide within the heterostructure results in high porosity and excellent conductivity. Due to enhanced electron and Na<sup>+</sup> transfer, as well as improved structural stability during the Na<sup>+</sup> insertion/extraction process, this heterogeneous structure exhibited exceptional Na<sup>+</sup> storage performance. Specifically, it exhibits a long-term cycling stability (217 mAh g<sup>−1</sup> at 10 C, 5000 cycles) and an ultrahigh rate capability (135 mAh g<sup>–1</sup>, 40 C). Analysis of electrode reaction kinetics suggests that Na<sup>+</sup> storage in the heterostructure is predominantly governed by a surface-controlled process. Our results provide a promising strategy for utilizing self-assembled heterostructures in advanced energy storage applications.</div></div>","PeriodicalId":100236,"journal":{"name":"ChemPhysMater","volume":"4 1","pages":"Pages 48-55"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPhysMater","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772571524000202","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
Transition metal oxides hold promise as electrode materials for energy-storage devices such as batteries and supercapacitors. However, achieving ideal electrode materials with high capacity, long-term cycling stability, and superb rate capability remains a challenge. In this study, we present a self-assembled heterogeneous structure consisting of TiO2 nanosheets derived from Ti3C2Tx MXene and reduced graphene oxide. This structure facilitates the formation of heterogeneous structures while establishing a conductive network. The restacking of porous TiO2 nanosheets and reduced graphene oxide within the heterostructure results in high porosity and excellent conductivity. Due to enhanced electron and Na+ transfer, as well as improved structural stability during the Na+ insertion/extraction process, this heterogeneous structure exhibited exceptional Na+ storage performance. Specifically, it exhibits a long-term cycling stability (217 mAh g−1 at 10 C, 5000 cycles) and an ultrahigh rate capability (135 mAh g–1, 40 C). Analysis of electrode reaction kinetics suggests that Na+ storage in the heterostructure is predominantly governed by a surface-controlled process. Our results provide a promising strategy for utilizing self-assembled heterostructures in advanced energy storage applications.