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BiSe is a promising material for anodes in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) due to its abundance, easy preparation, and high capacity. However, its practical application is hindered by low conductivity and significant volume variation during cycling, leading to poor rate capability and cycling stability. Herein, a novel composite consisting of BiSe nanoplates deposited on carbon cloth (CC) and encapsulated by reduced graphene oxide (rGO) has been designed and synthesized. The composite structure combines the advantages of the BiSe nanoplates, CC substrate, and rGO encapsulation, leading to enhanced electrochemical properties. The physical vapor deposition of BiSe nanoplates onto CC ensures a high loading of active material, while the rGO encapsulation provides a conductive and stable framework for the composite. This synergistic design allows for improved electron and ion transport, as well as efficient accommodation of the volume changes during cycling. In LIBs, the composite demonstrates a high reversible capacity of 467.5 mAh/g at 0.1 A/g after 120 cycles. Moreover, it displays an outstanding rate capability, delivering a capacity of 398.6 mAh/g at 5.0 A/g. Similarly, in SIBs, the composite maintains a reversible capacity of 375.3 mAh/g at 0.1 A/g over 100 cycles and exhibits a high-rate capacity of 286.3 mAh/g at 5.0 A/g. This work represents a significant step forward in addressing the challenges associated with BiSe as an anode material, paving the way for the development of high-performance LIBs and SIBs.
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http://dx.doi.org/10.1016/j.jcis.2023.07.053 | DOI Listing |
Chem Commun (Camb)
September 2025
Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
Herein, 1,3,5-benzenetricarboxylate (BTC) intercalation and oxygen vacancy engineering are proposed to enhance the electrochemical performance of layered double hydroxide (LDH) nanosheets. The optimized LDH exhibits a remarkable capacity of 426 mAh g at 3 A g and 70% capacity retention after 15 000 cycles, attributed to improved ion transport, abundant active sites, and structural stability.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Chemistry, Dalian University of Technology, Dalian 116024, PR China; College of Environment and Chemical Engineering, Dalian University, Dalian 116622, China. Electronic address:
Aqueous batteries have become a prospective future energy storage system because of their low coefficient of cost and stability. However, their lower energy density limits their applications. Ammonium ions (NH) have a small hydration radius and light molar mass, and aqueous ammonium ion batteries (AAIBs) are anticipated for solving the inherent low-energy density problem of aqueous batteries.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo 255000, PR China. Electronic address:
Li/CF primary batteries are renowned for their exceptional energy density, yet their practical deployment is hindered by the inherently sluggish kinetics of the CF cathode. This study addresses this limitation by incorporating selenium (Se) into CF (denoted as CF/Se) via a facile low-temperature thermal treatment, significantly enhancing its electrochemical performance. Comprehensive spectroscopic and electrochemical analyses reveal that Se doping induces the formation of CSe bonds, which promote semi-ionic CF bonding, thereby accelerating Li diffusion and reducing charge transfer resistance.
View Article and Find Full Text PDFNano Lett
September 2025
School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei 430070, China.
Aqueous zinc-ion batteries (AZIBs) represent an environmentally benign energy storage alternative. However, the VO cathode suffers from limited cycling stability and rate capability due to structural instability, vanadium dissolution, and high desolvation energy caused by the large size of [Zn(HO)] deintercalation. Address these issues, we introduce a VO/VOPO (VOP) heterostructure that that reinforces the crystal structure to suppress vanadium dissolution and establishes a hydrophilic interface reducing the desolvation energy of Zn.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
School of Integrated Circuits, State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Huazhong University of Science and Technology, Wuhan, 430074, China.
Low-temperature rechargeable batteries face great challenges due to the sluggish reaction kinetics. Redox covalent organic frameworks (COFs) with porous structures provide a viable solution to accelerate the ionic diffusion and reaction kinetics at low temperatures. However, the applications of COFs in low-temperature batteries are still at their infancy stage.
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