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Aqueous zinc-ion batteries (AZIBs) have aroused wide research enthusiasm due to their inherent safety, cost-effectiveness and sustainability advantages. However, the parasitic side reactions and rampant dendrite growth of Zn anodes seriously limit their application. In this work, a highly crystalline hydrogen-bonded organic framework (HOF-DAT) is prepared and evaluated as a protective coating for Zn anodes for the first time. The hydrogen-bonded networks as well as abundant polar groups prevent free water from contacting the Zn anode and assist Zn de-solvation, thus significantly suppresses side reactions. Meanwhile, the ordered and stable porous structure could provide numerous channels, which ensure uniform and rapid transport/deposition for Zn, thus guiding Zn flux and blocking interfacial corrosion. Benefiting from these advantages, the symmetric cell of HOF-DAT@Zn achieves stable plating/stripping of more than 780 h with lower polarization voltage. In addition, the HOF-DAT@Zn//NHVO full cell also delivers a higher initial discharge capacity of 355.5 mAh g at 1 A g and good reversible capacity of 248 mAh g after 200 cycles. This work offers insights for the design of HOF-based protective coating for AZIBs.
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http://dx.doi.org/10.1016/j.jcis.2025.138147 | DOI Listing |
J Am Chem Soc
September 2025
Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569 Stuttgart, Germany.
Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (HO).
View Article and Find Full Text PDFACS Omega
September 2025
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China.
For a long time, it was believed that the monoclinic potassium dihydrogen phosphate (KDP) crystal could not grow directly in solution, unlike its deuterated isomer DKDP. This perception was overturned when the crystal was observed to crystallize in highly supersaturated aqueous solutions. Till now, the phase stability of the monoclinic KDP remains unknown.
View Article and Find Full Text PDFACS Omega
September 2025
Department of Chemistry, College of Science, Wollo University, PO Box, 1145 Dessie, Ethiopia.
The increasing pollution of water bodies from various industrial wastewater discharges has raised significant environmental concerns because these effluents contain toxic, nonbiodegradable compounds that pose serious risks to living organisms. In particular, the textile and pharmaceutical industries routinely use dyes that severely degrade water quality and lead to significant environmental issues. Therefore, effective removal of these dyes from industrial wastewater is crucial for mitigating pollution.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Space Power-Sources, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, 150001, China.
Disordered rock-salt LiVO (DRX-LVO) anode exhibits distinctive 3D Li percolation transport networks, which offers the unique advantage for ultra-charging. However, the existing chemical lithiation preparation routes not only pose safety risks due to the use of highly reactive reagents but also inevitably result in products with poor crystallinity. Investigating the origin, impact, and strategies for crystallinity degradation is pivotal for advancing the industrialization of chemical lithiation.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Clemens-Schöpf-Institut für Organische Chemie und Biochemie, Technische Universität Darmstadt, Peter-Grünberg-Str. 16, 64287 Darmstadt, Germany.
Helical structures are ubiquitous in nature and exhibit fascinating properties. They are inherently chiral, and many rely on hydrogen bonds to stabilize their conformation. Homopolypeptides of the glutamate type form α-helical secondary structures and are considered rigid-rod polymers.
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