Hard carbon exhibits high theoretical capacity for sodium-ion batteries. However, its practical application suffers from low electric conductivity, poor electrochemical stability, and sluggish kinetics. To tackle these challenges, novel nitrogen-doped carbon spheres with mesopores, ultrathin nanostructure, and optimal graphitization are prepared by a three-step procedure. We find that the as-prepared sample (NMCSs-800) with an optimal structure and nitrogen content delivers a high reversible sodium storage capacity of 334.7 mA h/g at 50 mA/g and an ultrahigh rate performance of 93.9 mA h/g at 5 A/g, which is better than most state-of-the-art carbon materials. The improved energy storage capacity is attributed to its unique architecture and optimal nitrogen doping, which provide abundant active sites, defects, and voids. Moreover, kinetic analysis and in situ Raman spectroscopy results reveal adsorption and adsorption-intercalation mechanisms for Na storage in hard carbon at the slope region above 0.3 V and the other slope region of 0.3-0.02 V, respectively. We believe that our findings provide a novel tactic to design elaborate nanomaterials for the high-performance sodium-ion battery.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.8b17473 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Materials Science and Engineering, Northeastern University, Shenyang 110819, PR China.
The NASICON-type NaV(PO) (NVP) is recognized as a potential cathode material for Na-ion batteries (SIBs). Nevertheless, its inherent small electronic conductivity induces limited cycling stability and rate performance. Carbon coating, particularly N-doped carbon, has been identified as an effective strategy to address these challenges.
View Article and Find Full Text PDFLangmuir
January 2025
School of Physics, Beihang University, Beijing 100191, People's Republic of China.
Potassium manganese-based Prussian blue analogs (KMn-HCF) hold great potential as cathodes for sodium-ion batteries (SIBs). However, the rapid synthesis process often results in excessively small particle sizes, increasing surface area and thereby intensifying side reactions with the electrolyte, which can damage the cathode electrolyte interface (CEI) and diminish cycling stability. Herein, we designed a topological phase transition strategy to assemble small KMn-HCF particles into a 600 nm cubic superstructure.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Material, Shandong University, Jinan 250100, China.
Architecting Prussian blue analogue (PBA) cathodes with optimized synergistic bimetallic reaction centers is a paradigmatic strategy for devising high-energy sodium-ion batteries (SIBs); however, these cathodes usually suffer from fast capacity fading and sluggish reaction kinetics. To alleviate the above problems, herein, a series of early transition metal (ETM)-late transition metal (LTM)-based PBA (Fe-VO, Fe-TiO, Fe-ZrO, Co-VO, and Fe-Co-VO) cathode materials have been conveniently fabricated via an "acid-assisted synthesis" strategy. As a paradigm, the FeVO-PBA (FV) delivers a superb rate capability (148.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China.
Advancements in the development of fast-charging and long-lasting microstructured alloying anodes with high volumetric capacities are essential for enhancing the operational efficiency of sodium-ion batteries (SIBs). These anodes, however, face challenges such as declined cyclability and rate capability, primarily due to mechanical degradation reduced by significant volumetric changes (over 252%) and slow kinetics of sodium-ion storage. Herein, we introduce a novel anode design featuring densely packed bismuth (Bi) embedded within highly conductive carbon microspheres to overcome the aforementioned challenges.
View Article and Find Full Text PDFDalton Trans
January 2025
School of Materials Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang 212100, Jiangsu, China.
Three new sodium manganese fluoro-pyrophosphate compounds, namely, NaMn(PO)F (I), NaMn(PO)F (II), and NaMn(PO)F (III), have been synthesized by heating a mixture of NaPF, NaPOF or NaHPO with different Mn sources in NaNO and KNO fluxes. The structures of the title compounds were characterized single-crystal X-ray diffraction (XRD). II is characteristic of a shell of Na ions that encloses one [Mn(PO)F] unit, whereas I and III reveal three-dimensional (3D) frameworks that consist of MnO, Mn/NaOF octahedra or MnO octahedra and distorted MnO square pyramids with PO units, where Na cations reside in different-membered ring one-dimensional (1D) tunnels.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!