Photons, Excitons, and Electrons in Covalent Organic Frameworks
Dominic Blätte1, Frank Ortmann2, Thomas Bein1
1Department of Chemistry and Center for NanoScience, University of Munich (LMU), Butenandtstr. 5-13, 81377 Munich, Germany.
Journal of the American Chemical Society
|November 18, 2024
Summary
Covalent organic frameworks (COFs) offer tunable optoelectronic properties by controlling their structure. These porous materials show promise in applications like photocatalysis and photovoltaics.
Area of Science:
- Materials Science
- Chemistry
- Nanotechnology
Background:
- Covalent organic frameworks (COFs) are crystalline porous materials constructed from molecular building blocks.
- COFs offer diverse architectures with tunable properties for various applications.
- Recent research highlights the optoelectronic potential of COFs.
Purpose of the Study:
- To explore the relationship between the structural features of COFs and their optoelectronic properties.
- To review the impact of building blocks, connectivity, and morphology on optoelectronic behavior.
- To discuss emerging applications of COFs in optoelectronics, particularly photocatalysis and photoelectrochemistry.
Main Methods:
- Analysis of molecular building blocks and linkage chemistry.
- Investigation of layer stacking in 2D COFs.
- Control over defects, morphology, and thin film synthesis.
- Theoretical modeling of structural, electronic, and dynamic features.
- Review of recent applications in photocatalysis and photoelectrochemistry.
Main Results:
- Structural control over COFs allows tuning of photon absorption and emission.
- COFs can generate excitons and charge carriers for optoelectronic applications.
- The linkage chemistry and framework topology significantly influence electronic properties.
- Defect engineering and thin-film synthesis enable enhanced performance.
Conclusions:
- COFs present a powerful platform for designing materials with tailored optoelectronic properties.
- Significant progress has been made in understanding and controlling COF optoelectronics.
- Future research should focus on addressing current challenges and exploring new applications.
More Related Videos
Related Concept Videos
MO Theory and Covalent Bonding
10.3K
The molecular orbital theory describes the distribution of electrons in molecules in a manner similar to the distribution of electrons in atomic orbitals. The region of space in which a valence electron in a molecule is likely to be found is called a molecular orbital. Mathematically, the linear combination of atomic orbitals (LCAO) generates molecular orbitals. Combinations of in-phase atomic orbital wave functions result in regions with a high probability of electron density, while...
10.3K
Crystal Field Theory - Octahedral Complexes
26.2K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
26.2K
Covalent Bonding and Lewis Structures
48.8K
Compared to ionic bonds, which results from the transfer of electrons between metallic and nonmetallic atoms, covalent bonds result from the mutual attraction of atoms for a “shared” pair of electrons.
48.8K
Crystal Field Theory - Tetrahedral and Square Planar Complexes
41.6K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
41.6K
Network Covalent Solids
13.4K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
13.4K
π Electron Effects on Chemical Shift: Overview
1.1K
An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
1.1K


