{"title":"Facile Fabrication of Porous MoSe2/Carbon Microspheres via the Aerosol Process as Anode Materials in Potassium-Ion Batteries","authors":"D. Jo, Seung-Keun Park","doi":"10.3390/batteries10010025","DOIUrl":null,"url":null,"abstract":"Recently, potassium-ion batteries (KIBs) have attracted significant interest due to a number of factors, including the growing demand for energy and limited lithium resources. However, their practical use is hampered by poor cycling stability due to the large size of K+. Therefore, it is critical to develop a structural design that effectively suppresses large volume changes. This study presents a simple method of using a salt template to fabricate porous microspheres (p-MoSe2@C MS) of MoSe2 and a carbon matrix as anode materials in KIBs. These microspheres have a distinct porous design, with uniformly distributed MoSe2 nanocrystals embedded in the carbon matrix to prevent MoSe2 overgrowth due to material diffusion during heat treatment. The manufacturing process combined one-step spray drying with recyclable NaCl as a hard template. Through a two-step thermal process under an inert atmosphere, the initial dextrin, NaCl, and Mo salt microspheres were converted into a p-MoSe2@N MS composite. The carbon structure derived from the dextrin maintained the shape of the microspheres when NaCl was removed, ensuring no overgrowth of MoSe2. This well-designed porous structure improves the interaction with the electrolyte, facilitating the transport of ions and electrons and reducing the K+ diffusion distances. In addition, the porous carbon structure accommodates large volume changes during cycling and maintains its structural strength. As a result, p-MoSe2@C MS composite exhibits superior electrochemical properties, with remarkable capacity, long-term cycling stability (193 mA h g−1 after 500 cycles at 2.0 A g−1), and rate capability.","PeriodicalId":8755,"journal":{"name":"Batteries","volume":"42 22","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Batteries","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3390/batteries10010025","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Recently, potassium-ion batteries (KIBs) have attracted significant interest due to a number of factors, including the growing demand for energy and limited lithium resources. However, their practical use is hampered by poor cycling stability due to the large size of K+. Therefore, it is critical to develop a structural design that effectively suppresses large volume changes. This study presents a simple method of using a salt template to fabricate porous microspheres (p-MoSe2@C MS) of MoSe2 and a carbon matrix as anode materials in KIBs. These microspheres have a distinct porous design, with uniformly distributed MoSe2 nanocrystals embedded in the carbon matrix to prevent MoSe2 overgrowth due to material diffusion during heat treatment. The manufacturing process combined one-step spray drying with recyclable NaCl as a hard template. Through a two-step thermal process under an inert atmosphere, the initial dextrin, NaCl, and Mo salt microspheres were converted into a p-MoSe2@N MS composite. The carbon structure derived from the dextrin maintained the shape of the microspheres when NaCl was removed, ensuring no overgrowth of MoSe2. This well-designed porous structure improves the interaction with the electrolyte, facilitating the transport of ions and electrons and reducing the K+ diffusion distances. In addition, the porous carbon structure accommodates large volume changes during cycling and maintains its structural strength. As a result, p-MoSe2@C MS composite exhibits superior electrochemical properties, with remarkable capacity, long-term cycling stability (193 mA h g−1 after 500 cycles at 2.0 A g−1), and rate capability.