Owing to the synergistic combination of a hybrid organic-inorganic nature and a chemically active porous structure, metal-organic frameworks have emerged as a new class of crystalline materials. The current trend in the chemical industry is to utilize such crystals as flexible hosting elements for applications as diverse as gas and energy storage, filtration, catalysis, and sensing. From the physical point of view, metal-organic frameworks are considered molecular crystals with hierarchical structures providing the structure-related physical properties crucial for future applications of energy transfer, data processing and storage, high-energy physics, and light manipulation. Here, the perspectives of metal-organic frameworks as a new family of functional materials in modern physics are discussed: from porous metals and superconductors, topological insulators, and classical and quantum memory elements, to optical superstructures, materials for particle physics, and even molecular scale mechanical metamaterials. Based on complementary properties of crystallinity, softness, organic-inorganic nature, and complex hierarchy, a description of how such artificial materials have extended their impact on applied physics to become the mainstream in material science is offered.
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http://dx.doi.org/10.1002/advs.201900506 | DOI Listing |
Small
January 2025
Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
The ligands in metal-organic framework (MOF) play as light absorption center and transfer photogenerated electrons to metal node through ligand-to-metal charge transfer (LMCT) during photocatalysis, and energy utilization efficiency is strongly restricted by the light inertness of ligands. Herein, a ligand updating strategy is proposed by inserting energy centers to MOFs to activate the inherent ligands, realizing boosting hot electron generation and photocatalytic activities via the cascaded proceeding of energy transfer and charge transfer. By taking PCN-777 (a zeotype mesoporous Zr-containing MOF) as an example, this study shows that the embedded energy center of 1-pyrenecarboxylic acid (PCA) can activate the inherent ligand of PCN-777 through triplet-triplet energy transfer, where triplet excitons would dissociate into photocarriers migrating to the Zr metal cluster via LMCT process.
View Article and Find Full Text PDFFront Chem
December 2024
Department of Chemistry, University of Wyoming, Laramie, WY, United States.
Covalent integration of polymers and porous organic frameworks (POFs), including metal-organic frameworks (MOFs), covalent organic frameworks (COFs) and hydrogen-bonded organic frameworks (HOFs), represent a promising strategy for overcoming the existing limitations of traditional porous materials. This integration allows for the combination of the advantages of polymers, i.e.
View Article and Find Full Text PDFChemSusChem
January 2025
Guangxi University, School of Resource, Environments and Materials, CHINA.
Lithium (Li) metal anodes (LMAs), which show a great potential in constructing high-specific-energy-density Li metal batteries (LMBs), have abstracted wide research interest. However, the generation of Li dendrites and the repeated change of volume upon Li plating/stripping severely block the practical commercialization of LMBs. Herein, the functional carbon fibers (CFs) decorated with ZnO embedded carbon cage (ZnO@C-d-CFs) were fabricated successfully by a two-step route including the in-situ growth of Zn-based metal organic frameworks (MOFs) and subsequent carbonization process, which enriched the lithiophilic sites of CFs host and improved Li+ kinetics of Li+ plating/stripping.
View Article and Find Full Text PDFChem Asian J
January 2025
Jadavpur University, Department of Chemistry, INDIA.
Three different two dimensional Cd(II)-based metal-organic frameworks (MOFs) have been synthesized by utilizing same N,N'-donor ligand and three different functionalized dicarboxylate linkers namely isophthalate, 5-nitroisophthalate and 5-hydroxyisophthalate for compound 1, 2 and 3 respectively. The compounds that are isoreticular bi-walled 2D frameworks, show dual fluorescence emission spectra for their π-π* and n-π* excitation. Compound 1 is consists of unsubstituted bridging isophthalate whereas 2 and 3 are made with bridging isophthalate that are substituted by electron withdrawing -NO2 group and electron donating -OH group respectively.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Tianjin University of Technology, Institute for New Energy Materials and Low Carbon Technologies, 300384, Tianjin, CHINA.
Biphasic system not only presents a promising opportunity for complex catalytic processes, but also is a grand challenge in efficient tandem reactions. As an emerging solar-to-chemical conversion, the visible-light-driven and water-donating hydrogenation combines the sustainability of photocatalysis and economic-value of hydrogenation. However, the key and challenging point is to couple water-soluble photocatalytic hydrogen evolution reaction (HER) with oil-soluble hydrogenation.
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