In the face of escalating environmental challenges such as fossil fuel dependence and water pollution, innovative solutions are essential for sustainable development. In this regard, zeolitic imidazolate frameworks (ZIFs), specifically ZIF-8, act as promising photocatalysts for environmental remediation and renewable energy applications. ZIF-8, a subclass of metal-organic frameworks (MOFs), is renowned for its large specific surface area, high porosity, rapid electron transfer ability, abundant functionalities, ease of designing, controllable properties, and remarkable chemical and thermal stability. However, its application as a standalone photocatalyst is limited by issues such as particle aggregation, poor water stability, and insufficient visible light absorption. By integrating ZIF-8 with various photoactive materials to form composite catalysts, these drawbacks can be mitigated, leading to enhanced photocatalytic efficiency. The review discusses the synthesis, properties, and applications of ZIF-8-based photocatalysts in light-driven H evolution, HO evolution, CO reduction, and dye and drug degradation. It also highlights the challenges and future research directions in developing cost-effective, scalable, and environmentally friendly ZIF-8 composites for industrial applications. The potential of ZIF-8 composites to contribute to sustainable global energy solutions and environmental cleanup is significant, yet further exploration is required to harness their capabilities thoroughly.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/d4dt02662d | DOI Listing |
J Am Chem Soc
January 2025
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Although microenvironments surrounding single-atom catalysts (SACs) have been widely demonstrated to have a remarkable effect on their catalytic performances, it remains unclear whether the local structure beyond the secondary coordination shells works as well or not. Herein, we employed a series of metal-organic frameworks (MOFs) with well-defined and tunable second-beyond coordination spheres as model SAC electrocatalysts to discuss the influence of long-distance structure on the ammonia synthesis from nitrate, which were synthesized and denoted as Cu-NDI-X (X = NMe, H, F). It is first experimentally confirmed that the remote substitution of function groups beyond the secondary coordination sphere can remarkably affect the activity of ammonia synthesis.
View Article and Find Full Text PDFSmall
January 2025
College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
The photocatalytic reduction of CO in water to produce fuels and chemicals is promising while challenging. However, many photocatalysts for accomplishing such challenging task usually suffer from unspecific catalytic active sites and the inefficient charge carrier's separation. Here, a site-specific single-atom Ni/TiO catalyst is reported by in situ topological transformation of Ni-Ti-EG bimetallic metal-organic frameworks.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
January 2025
Furman University, Greenville, South Carolina 29613, United States.
Surface-anchored metal-organic frameworks (surMOFs) are crystalline, nanoporous, supramolecular materials mounted to substrates that have the potential for integration within device architectures relevant for a variety of electronic, photonic, sensing, and gas storage applications. This research investigates the thin film formation of the Cu-BDC (copper benzene-1,4-dicarboxylate) MOF system on a carboxylic acid-terminated self-assembled monolayer by alternating deposition of solution-phase inorganic and organic precursors. X-ray diffraction (XRD) and atomic force microscopy (AFM) characterization demonstrate that crystalline Cu-BDC thin films are formed via Volmer-Weber growth.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
January 2025
Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States.
Porous adsorbents are a promising class of materials for the direct air capture of CO (DAC). Practical implementation of adsorption-based DAC requires adsorbents that can be used for thousands of adsorption-desorption cycles without significant degradation. We examined the potential degradation of adsorbents by a mechanism that appears to have not been considered previously, namely, ozonolysis by trace levels of ozone from ambient air.
View Article and Find Full Text PDFChem Sci
January 2025
Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education and Faculty of Chemistry, Northeast Normal University 5268 Renmin Street Changchun 130024 P. R. China
Two-dimensional conductive metal-organic frameworks (2D c-MOFs) with high electrical conductivity and tunable structures hold significant promise for applications in metal-ion batteries. However, the construction of 3D interpenetrated c-MOFs for applications in metal-ion batteries is rarely reported. Herein, a 3D four-fold interpenetrated c-MOF (Cu-DBC) constructed by conjugated and contorted dibenzo[,]chrysene-2,3,6,7,10,11,14,15-octaol (DBC) ligands is explored as an advanced cathode material for sodium-ion batteries (SIBs) for the first time.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!