Cheng Liu , Yi Wen , Gaoya Ren , Yaxuan Li , Qianqian Sun , Shenghui Shen , Zhujun Yao , Yefeng Yang
{"title":"Flower-like Fe-doped NiSe2/C hybrid spheres fabricated by a glucose-intercalation strategy for enhanced sodium storage properties","authors":"Cheng Liu , Yi Wen , Gaoya Ren , Yaxuan Li , Qianqian Sun , Shenghui Shen , Zhujun Yao , Yefeng Yang","doi":"10.1016/j.chphma.2024.01.004","DOIUrl":null,"url":null,"abstract":"<div><p>Nickel diselenide (NiSe<sub>2</sub>), which has a high theoretical capacity, has attracted considerable attention as a promising anode material for sodium-ion batteries (SIBs). Nevertheless, the intrinsically low conductivity, large volume variation, and significant aggregation of NiSe<sub>2</sub> during sodiation/desodiation remain significant obstacles to its application. Herein, we report flower-like Fe-doped NiSe<sub>2</sub>/C hybrid spheres (denoted as Fe-NiSe<sub>2</sub>/C) fabricated by a glucose intercalation strategy for efficient sodium storage. These Fe-NiSe<sub>2</sub>/C hybrid spheres are composed of thin porous carbon nanosheets decorated with Fe-NiSe<sub>2</sub> nanoparticles. In situ introduced carbon nanosheets derived from intercalated glucose accompanied by moderate Fe doping in NiSe<sub>2</sub> nanoparticles can provide accelerated ion/electron transfer kinetics through fast ion channels in the flower-like architecture and intimately contacted interfaces between NiSe<sub>2</sub> and carbon nanosheets as well as maintain structural integrity by alleviating volume variation. Consequently, the optimal anode of the Fe-NiSe<sub>2</sub>/C hybrid spheres delivered a high discharge capacity of 415 mAh g<sup>−1</sup> at 0.5 A g<sup>−1</sup>, outstanding rate capability (243 mAh g<sup>−1</sup> at 5 A g<sup>−1</sup>), and significantly enhanced cycling stability (388 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup> over 200 cycles). This work offers an efficient and valuable strategy for realizing tailored heteroatom doping in transition metal selenides, accompanied by an in situ combination of conductive carbonaceous networks for advanced alkali metal ion batteries.</p></div>","PeriodicalId":100236,"journal":{"name":"ChemPhysMater","volume":"3 2","pages":"Pages 220-229"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772571524000044/pdfft?md5=64d9c59893b67262581be2672adb8f61&pid=1-s2.0-S2772571524000044-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemPhysMater","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772571524000044","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
Nickel diselenide (NiSe2), which has a high theoretical capacity, has attracted considerable attention as a promising anode material for sodium-ion batteries (SIBs). Nevertheless, the intrinsically low conductivity, large volume variation, and significant aggregation of NiSe2 during sodiation/desodiation remain significant obstacles to its application. Herein, we report flower-like Fe-doped NiSe2/C hybrid spheres (denoted as Fe-NiSe2/C) fabricated by a glucose intercalation strategy for efficient sodium storage. These Fe-NiSe2/C hybrid spheres are composed of thin porous carbon nanosheets decorated with Fe-NiSe2 nanoparticles. In situ introduced carbon nanosheets derived from intercalated glucose accompanied by moderate Fe doping in NiSe2 nanoparticles can provide accelerated ion/electron transfer kinetics through fast ion channels in the flower-like architecture and intimately contacted interfaces between NiSe2 and carbon nanosheets as well as maintain structural integrity by alleviating volume variation. Consequently, the optimal anode of the Fe-NiSe2/C hybrid spheres delivered a high discharge capacity of 415 mAh g−1 at 0.5 A g−1, outstanding rate capability (243 mAh g−1 at 5 A g−1), and significantly enhanced cycling stability (388 mAh g−1 at 1 A g−1 over 200 cycles). This work offers an efficient and valuable strategy for realizing tailored heteroatom doping in transition metal selenides, accompanied by an in situ combination of conductive carbonaceous networks for advanced alkali metal ion batteries.