Amorphous-crystalline transition-induced hollowing of covalent organic frameworks: a structural evolution boosting
Cuicui Shao1, Zhijian Li1, Yuxin Sun1
1Jiangxi Province Key Laboratory of Organic Functional Molecules, Institute of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang, 330013, P. R. China. lizhijianhdd@163.com.
Materials Horizons
|December 2, 2025
Summary
A novel self-template method creates stable hollow covalent organic frameworks (COFs) using Ostwald ripening. These hollow COFs show enhanced uranium adsorption, offering a promising strategy for efficient removal.
Area of Science:
- Materials Science
- Nanotechnology
- Environmental Chemistry
Background:
- Hollow covalent organic frameworks (COFs) offer unique structural advantages for various applications.
- Controllable synthesis of uniform and stable hollow COFs presents a significant challenge in materials science.
Purpose of the Study:
- To develop a facile and effective self-template method for preparing hollow COFs.
- To investigate the morphological evolution and structural properties of the synthesized hollow COFs.
- To evaluate the uranium adsorption performance of hollow COFs functionalized with phosphate groups.
Main Methods:
- Utilized Ostwald ripening mechanism under environmental conditions for self-templating.
- Employed time-resolved structural analyses to track morphological changes from solid to hollow structures.
- Synthesized phosphorylated hollow COFs (PA-H-COF) for uranium adsorption studies.
Main Results:
- Achieved hierarchical hollow-flower COFs (H-COF) with high crystallinity and a specific surface area of 534.99 m² g⁻¹.
- Demonstrated superior uranium adsorption capacity (296.7 mg g⁻¹) for PA-H-COF compared to non-hollow counterparts.
- Observed significant uranium adsorption (7.38 mg g⁻¹) from actual seawater within 20 days.
Conclusions:
- The proposed self-template method provides a viable route to uniform and stable hollow COFs.
- The hierarchical structure of hollow COFs enhances active site exposure, leading to improved uranium adsorption.
- Hollow phosphate functionalized COFs show great potential for efficient uranium removal from aqueous solutions.
Related Concept Videos
Crystal Field Theory - Octahedral Complexes
30.4K
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...
30.4K
Crystal Field Theory - Tetrahedral and Square Planar Complexes
47.9K
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,...
47.9K
Polymer Classification: Crystallinity
3.7K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
3.7K
Structures of Solids
17.3K
Solids in which the atoms, ions, or molecules are arranged in a definite repeating pattern are known as crystalline solids. Metals and ionic compounds typically form ordered, crystalline solids. A crystalline solid has a precise melting temperature because each atom or molecule of the same type is held in place with the same forces or energy. Amorphous solids or non-crystalline solids (or, sometimes, glasses) which lack an ordered internal structure and are randomly arranged. Substances that...
17.3K
Metallic Solids
20.4K
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
20.4K
Network Covalent Solids
15.9K
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...
15.9K


