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Conductive metal-organic frameworks (C-MOFs) have received extensive interest in high-performance zinc-ion batteries (ZIBs) owing to multi-redox sites and high electrical conductivity. Here, we present a π-d C-MOF by coordinating 2,3,5,6-tetraaminobenzoquinone (TABQ) ligands with Cu ions (2D Cu-TABQ) acting as cathodes for ZIBs. Benefiting from a triple active center (Cu, C=O, and C=N), 2D Cu-TABQ shows an ultra-high reversible capacity of 297.7 mAh g at 0.2 A g. Meanwhile, 2D Cu-TABQ also has superior cycle stability with a capacity of up to 98.2 mAh g after 1000 times at 2.0 A g. Considering the instability of the ligand bonds of C-MOFs in aqueous electrolytes, this work uses gel electrolytes to reduce the dissolution of organic ligands into the electrolyte, thus suppressing the shuttle effect, significantly improving the cycling stability of 2D Cu-TABQ. The flexible battery assembled by 2D Cu-TABQ shows excellent capacity retention (64.4 %) after 50 times at 0.2 A g, which is significantly better than 36.4 % in the common electrolyte, as well as outstanding bending resistance and electrochemical properties at different folding angles. This investigation will highlight the electrochemical application of C-MOFs in flexible zinc ion batteries and offer novel ideas for the structural design of cathodes with multiple active centers.
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http://dx.doi.org/10.1002/cssc.202401606 | DOI Listing |
Small
September 2025
School of Materials Science and Engineering, State Key Laboratory of Silicon and Advanced Semiconductor Materials, Zhejiang University, Hangzhou, 310027, P. R. China.
High-concentration electrolytes (HCEs) face inherent challenges such as high viscosity and diminished ionic conductivity caused by the formation of three-dimensional (3D) anion networks, which limit their practical applications. In this study, it is demonstrated that encapsulating HCEs within metal-organic frameworks (MOFs) effectively disrupts these 3-D networks, resulting in significantly enhanced ionic conductivity. Raman spectroscopy, nuclear magnetic resonance (NMR), and molecular dynamics (MD) simulations reveal a significant reduction in aggregates (AGGs)-state anion within MOF-confined electrolytes, confirming the reconstruction of the solvation environment.
View Article and Find Full Text PDFSmall
September 2025
Department of Chemistry, Jadavpur University, Kolkata, 700032, India.
The design of a rare combination of interpenetrated and catenated 3D+2D→3D MOF {[Cd(dim)(dht)(HO)](Sol)} (1), with a unique network and extreme pH stability, has been developed for exceptional ionic conduction across a wide range of temperature and humidity conditions. The bare pore derivative of 1 (1') features remarkable structural flexibility and large pores accessible to encapsulate molecules such as NH, HCl, and KOH, enabling it to function as an efficient conductor for both proton and hydroxide ions. 1' demonstrates substantial thermal-influenced proton conductivity of 4.
View Article and Find Full Text PDFResearch (Wash D C)
September 2025
Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan 250061, China.
With the rapid advancement of communication technologies, issues of electromagnetic pollution and electromagnetic compatibility have become increasingly severe, heightening the demand for high-performance electromagnetic wave absorption materials. Metal-organic frameworks (MOFs) have flourished in this field owing to their chemical tunability, high porosity, tailored topological structures, and functionality. MOF-derived composites exhibit diverse loss mechanisms and heterogeneous structures, achieving lightweight, broadband, and highly efficient absorption.
View Article and Find Full Text PDFChemistryOpen
September 2025
CMC UMR 7140, CNRS, Université de Strasbourg, Strasbourg, F-67000, France.
Two series of robust pillared metal-organic frameworks (MOFs) are obtained under solvothermal conditions by combining a metal salt with either Hbpdc, biphenyl-4,4'-dicarboxylic acid, or Hpda, 1,4-phenylenediacrylic acid, forming 2D layers, which are pillared by L, an alloxazine derivative of 1,4-di(pyridin-4-yl)benzene using a one-pot three-component strategy. Crystallographic studies reveal the formation of two isomorphous series of compounds, namely 1-M (from Hbpdc with M = Co, Ni, Cu, and Zn) and 2-M (from Hpda with M = Co or Cu). The multifunctional compounds have high decomposition temperatures, and their sorption properties were measured, revealing relatively low surface areas.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225009, P. R. China.
Lithium-sulfur batteries (LSBs) hold great potential as next-generation energy storage systems due to their high theoretical energy density and relatively low cost. However, their practical application is hindered by issues such as the shuttle phenomenon caused by soluble lithium polysulfides (LiPSs), slow redox reaction rates, and unsatisfactory cycling stability. In this study, novel conjugated metal-organic frameworks, MM″(HHTP) (M, M″ = Ni, Co, Cu) is reported, as a functional coating on polypropylene (PP) separators.
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