Coupling ion exclusion and interaction screening within sub-nanoconfinement channels in novel porous material membranes hold great potential to realize highly efficient ion sieving, particularly for high-performance lithium-ion extraction. Diverse kinds of advanced membranes have been previously reported to realize this goal but with moderate performance and complex operations gained. Herein, these issues are circumvented by preparing the consecutive and intact imine-linked three-dimensional covalent organic framework (i.e., COF-300) membranes via a simple solvothermal approach and employing the intrinsically interconnected sub-1 nm one-dimensional channels for exceptional lithium-ion sieving. The synthesized membranes with highly charged angstrom scale channels of ≈0.78 nm achieve an excellent Li permeance (0.123 mol m h) with an ultrahigh Li/Mg of 36 in the binary system. The experimental measurement and theoretical calculation reveal that a channel size right exactly between Li and Mg enables restricted Mg penetration. Meanwhile, the ion affinity interaction screening with imine groups further strengthens the fast Li permeability but severely suppresses the Mg passage. In particular, the synthesized three-dimensional covalent organic framwork membranes also have a remarkable separation performance during a long-term operation test without sacrificing trade-off, demonstrating chemistry stability and mechanical integrity under the high-salinity aqueous environment.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.202415509 | DOI Listing |
Chem Sci
December 2024
Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China Hefei Anhui 230026 China
The packing of organic molecular crystals is often dominated by weak non-covalent interactions, making their rearrangement under external stimuli challenging to understand. We investigate a pressure-induced single-crystal-to-single-crystal (SCSC) transformation between two polymorphs of 2,4,5-triiodo-1-imidazole using machine learning potentials. This process involves the rearrangement of halogen and hydrogen bonds combined with proton transfer within a complex solid-state system.
View Article and Find Full Text PDFAdv Mater
January 2025
College of Energy, Key Laboratory of Core Technology of High Specific Energy Battery and Key Materials for Petroleum and Chemical Industry, Soochow University, Suzhou, 215006, China.
Coupling ion exclusion and interaction screening within sub-nanoconfinement channels in novel porous material membranes hold great potential to realize highly efficient ion sieving, particularly for high-performance lithium-ion extraction. Diverse kinds of advanced membranes have been previously reported to realize this goal but with moderate performance and complex operations gained. Herein, these issues are circumvented by preparing the consecutive and intact imine-linked three-dimensional covalent organic framework (i.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Science and Technology Beijing, School of Chemistry and Biological Engineering, CHINA.
Designing and realizing new topologies represent one of the most important ways toward developing new structures and functionalities for molecule-based frameworks including SOFs, MOFs, and COFs. Herein, Aldol condensation between 5,10,15,20-tetrayl(tetrakis(([1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde)))-porphyrin (TTEP) and 2,4,6-trimethyl-1,3,5-triazine (TMT) affords the vinylene-linked 3D covalent organic framework Por-COF-cya. Powder X-ray diffraction (PXRD) in combination with structural simulation reveals its high crystalline structure with an unprecedented cya topology in the molecule-based frameworks reported thus far.
View Article and Find Full Text PDFNat Chem
January 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, People's Republic of China.
Three-dimensional (3D) covalent organic frameworks (COFs) hold significant promise for a variety of applications. However, conventional design approaches using regular building blocks limit the structural diversity of 3D COFs. Here we design and synthesize two 3D COFs, designated as JUC-644 and JUC-645, through a methodology that relies on using eight-connected building blocks with reduced symmetry.
View Article and Find Full Text PDFNat Chem
January 2025
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Atomically precise nanoclusters can be assembled into ordered superlattices with unique electronic, magnetic, optical and catalytic properties. The co-crystallization of nanoclusters with functional organic molecules provides opportunities to access an even wider range of structures and properties, but can be challenging to control synthetically. Here we introduce a supramolecular approach to direct the assembly of atomically precise silver nanoclusters into a series of nanocluster‒organic ionic co-crystals with tunable structures and properties.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!