{"title":"Deciphering the Impact of Graphene Oxide Incorporation on Structural, Chemical, and Electrochemical Properties of Na2Fe(SO4)2 Cathode Materials","authors":"Hai-Dong Dai, Hua-Bin Sun, Ya-Nan Jiang, Yu-Wei Chen, Xiao-Kai Ding, Chien-Te Chen, Chang-Yang Kuo, Zhi-Wei Hu, Lu-Lu Zhang, Xue-Lin Yang","doi":"10.1021/acs.nanolett.4c06048","DOIUrl":null,"url":null,"abstract":"The performance of polyanionic Na<sub>2</sub>Fe(SO<sub>4</sub>)<sub>2</sub> (NFS) cathode materials is hindered by their low electronic conductivity and is correlated to their structural and chemical instability. Herein, we incorporated graphene oxide (GO) to modify NFS materials, which can build a carbon layer on the surface and alleviate Na<sub>6</sub>Fe(SO<sub>4</sub>)<sub>4</sub> phase formation and Fe<sup>2+</sup> oxidation in the lattice. Meanwhile, the performance of NFS materials has been significantly improved, such as the capacity retention showing an increase from 56% to 87% after 200 cycles at 0.5 C with GO incorporation. Soft X-ray absorption spectra (sXAS) reveals that the bulk has higher reversibility of the reaction between Fe<sup>2+</sup> and Fe<sup>3+</sup> than the surface during cycling, which indicates the origin of cycling instability of NFS materials. These findings provide new insights into surface modification for the development of high performance NFS cathodes.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"3 1","pages":""},"PeriodicalIF":9.6000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.nanolett.4c06048","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The performance of polyanionic Na2Fe(SO4)2 (NFS) cathode materials is hindered by their low electronic conductivity and is correlated to their structural and chemical instability. Herein, we incorporated graphene oxide (GO) to modify NFS materials, which can build a carbon layer on the surface and alleviate Na6Fe(SO4)4 phase formation and Fe2+ oxidation in the lattice. Meanwhile, the performance of NFS materials has been significantly improved, such as the capacity retention showing an increase from 56% to 87% after 200 cycles at 0.5 C with GO incorporation. Soft X-ray absorption spectra (sXAS) reveals that the bulk has higher reversibility of the reaction between Fe2+ and Fe3+ than the surface during cycling, which indicates the origin of cycling instability of NFS materials. These findings provide new insights into surface modification for the development of high performance NFS cathodes.
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
- Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale
- Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies
- Modeling and simulation of synthetic, assembly, and interaction processes
- Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance
- Applications of nanoscale materials in living and environmental systems
Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.