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Magnesium-ion batteries (MIBs) are a "beyond Li-ion" technology that are hampered by Mg metal reactivity, which motivates the development of anode materials such as tin (Sn) with high theoretical capacity (903 mAh g). However, pure Sn is inactive for Mg storage. Herein, Mg alloying with Sn is enabled within dual-phase Bi-Sn anodes, where the optimal composition (BiSn) outperformed single-phase Bi and Sn electrodes to deliver high specific capacity (462 mAh g at 100 mA g), good cycle life (84% after 200 cycles), and significantly improved rate capability (403 mAh g at 1000 mA g). Density functional theory (DFT) calculations revealed that Mg alloys first with Bi and the subsequent formation of the MgBi//Sn interfaces is energetically more favorable compared to the individual MgBi and Sn phases. Mg insertion into Sn is facilitated when MgBi is present. Moreover, dealloying Mg from MgBi:MgSn systems requires the creation of Mg vacancies and subsequent Mg diffusion. Mg vacancy creation is easier for MgSn compared to MgBi, while the latter has slightly lower activated Mg-diffusion pathways. The computational findings point toward easier magnesiation/demagnesiation for BiSn alloys over pure Bi or pure Sn, corroborating the superior Mg storage performance of Bi-Sn electrodes over the corresponding single-phase electrodes.
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http://dx.doi.org/10.1021/acsami.4c11272 | DOI Listing |
Angew Chem Int Ed Engl
August 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, China.
Aqueous Mg-ion batteries (AMIBs) have attracted increasing interest due to their safety, fast kinetics, and sustainability. However, the development of AMIBs is hindered by the narrow electrochemical stability window (ESW) of electrolytes and electrode degradation. Here, a synergistic strategy, regulating both electrolyte and electrode structures, is proposed to enable high-performance AMIBs.
View Article and Find Full Text PDFDalton Trans
August 2025
College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China.
High entropy compounds (HECs) are a new type of multi-element material. They overcome the limitations of traditional energy storage materials. HECs achieve this through three key features: high entropy effect, lattice distortion, and element synergy.
View Article and Find Full Text PDFInt J Biol Macromol
August 2025
Centre for Advanced Materials Application of the Slovak Academy of Sciences, Dubravska cesta 9, 845 11 Bratislava, Slovakia; Polymer Institute of the Slovak Academy of Sciences, Dubravska cesta 9, 845 41 Bratislava, Slovakia. Electronic address:
The influence of the cellulosic fabrics (CF) surface chemistry on hosting nickel ferrite (NF) and its application in Al-air battery was studied. CFs were modified with acrylate monomer bearing positively (COOCHCHN(CH)Cl) or negatively (-COO(CH)SOK) charged functional groups at different degrees of graft-polymerization. NF was in-situ hydrothermally synthesized into the un/grafted-CF followed by in-situ polymerization of polyaniline (PANi) to enhance the electric conductivity nine orders of magnitude.
View Article and Find Full Text PDFSmall
September 2025
Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India.
The electrochemical performance and diffusion kinetics of a newly designed NASICON-type NaMnTiMo(PO)/C composite material is reported as a cathode for cost-effective sodium-ion batteries. A novel strategy of small Mo doping successfully stabilizes the sample having high Mn content in single-phase rhombohedral symmetry. The high-resolution microscopy analysis reveals nanocrystallites of around ∼18 nm, uniformly embedded within the semi-graphitic carbon matrix, which enhances the surface electronic conductivity and effectively shortens the sodium-ion diffusion path.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518060, China.
The development of high-performance Zn-ion batteries is hindered by sluggish reaction kinetics and inadequate redox activity in conventional vanadium-based cathodes. Herein, a thermal oxidation phase-engineering strategy is proposed to construct a comprising VSSe core and oxygen-enriched VO and VO interfaces triple-phase heterojunction cathode. This unique architecture leverages a significantly increased specific surface area, which facilitates rapid electrode-electrolyte interactions and boosts pseudocapacitive contributions.
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