Due to the excellent specific capacity and high working voltage, manganese oxide (MnO ) has attracted considerable attention for aqueous zinc-ion batteries (AZIBs). However, the irreversible structural collapse and sluggish ionic diffusion lead to poor rate capability and inferior lifespan. Herein, we proposed a novel organic/inorganic hybrid cathode of carbon-based poly(4,4'-oxybisbenzenamine)/MnO (denoted as C@PODA/MnO ) for AZIBs. Various in/ex situ analyses and theoretical calculations prove that PODA chains with C=N groups can provide a more active surface/interface for ion/electron mobility and zinc ion storage in the hybrid cathode. More importantly, newly formed Mn-N interfacial bonds can effectively promote ion diffusion and prevent Mn atoms dissolution, enhancing redox kinetics and structural integrity of MnO . Accordingly, C@PODA/MnO cathode exhibits high capacity (321 mAh g or 1.7 mAh cm at 0.1 A g ), superior rate performance (88 mAh g at 10 A g ) and excellent cycling stability over 2000 cycles. Hence, rational interfacial designs shed light on the development of organic/inorganic cathodes for advanced AZIBs.
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http://dx.doi.org/10.1002/anie.202212231 | DOI Listing |
Chem Commun (Camb)
January 2025
Laboratory of Advanced Materials, Aqueous Batteries Center, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, 200433, China.
Zinc metal is a promising anode material for zinc-ion batteries (ZIBs), but severe side reactions and dendrite formation hinder its commercialization. In this study, starch is introduced into the ZnSO electrolyte for stabilizing the Zn anode. With abundant hydroxyl groups, starch can reconstruct the H-bond system in the electrolyte, suppressing side reactions.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, PR China. Electronic address:
Vanadium dioxide (VO) has attracted significant attention in aqueous zinc ion batteries (AZIBs) owing to their desirable theoretical specific capacity originated from multiple electrons transfer reaction and special crystal structure. However, sluggish electrochemical kinetics leads to inferior electrochemical storage performance. Herein, rich vanadium vacancies were introduced in tunnel VO to boost Zn diffusion, increasing charge storage capacity and lengthen lifespan.
View Article and Find Full Text PDFChem Asian J
January 2025
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, 560012, India.
The growing energy demands have led to an increased attention towards the development of efficient energy storage devices. In this direction, aqueous rechargeable batteries have attracted considerable attention due to their affordability, environmental friendliness and quite importantly, safety. In the present studies, a two-dimensional copolymer of benzoquinone and pyrrole that is insoluble in aqueous solutions is explored as an electrode for aqueous, rechargeable divalent ion storage.
View Article and Find Full Text PDFChemistry
January 2025
Westlake University, School of Engineering, 18 Shilongshan Road, 310024, Hangzhou, CHINA.
Design and manufacture of cathode materials, with suitable pore structure and high electrical conductivity to matching zinc anode, solving the problem of dissolution and structural degradation of cathode materials for zinc ion batteries (ZIBs), is great significance to the development of ZIBs. Herein, Vanadium Nitride (VN) uniformly decorated N-doped micro/mesoporous carbon nanofibers (VN/N-MCNF) with appropriate porous and reactive sites for Zn2+ is prepared by using V-MOF, as important precursor via electrostatic spinning and pyrolysis technique. As a cathode electrode for ZIBs, the VN/N-MCNF is suitable for diffusion and adsorption of large-sized solvated structured [Zn(H2O)6]2+, for its abundant micro/mesoporous structure and good electrical conductivity.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Chemistry, University College London, London, WC1E 7JE, UK.
Long-standing challenges including notorious side reactions at the Zn anode, low Zn anode utilization, and rapid cathode degradation at low current densities hinder the advancement of aqueous zinc-ion batteries (AZIBs). Inspired by the critical role of capping agents in nanomaterials synthesis and bulk crystal growth, a series of capping agents are employed to demonstrate their applicability in AZIBs. Here, it is shown that the preferential adsorption of capping agents on different Zn crystal planes, coordination between capping agents and Zn ions, and interactions with metal oxide cathodes enable preferred Zn (002) deposition, water-deficient Zn ion solvation structure, and a dynamic cathode-electrolyte interface.
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