Carbon dioxide catalytic conversion (i. e., CO catalysis) is considered as one of the most promising technologies to control CO emissions, which is of great significance to build a sustainable society with green low-carbon cycle. In view of its thermodynamic stability and kinetic inertness, CO selective activation is still desired. Nowadays, the traditional strategy is to selectively capture and efficiently convert atmospheric CO into high value-added chemicals and fuels. Covalent triazine frameworks (CTFs) as a newly emerging and attractive kind of porous organic polymer (POP) have drawn worldwide attention among heterogeneous catalysis because of their nitrogen-rich porous structures and exceptional physicochemical stabilities. In this Minireview, the focus was mainly placed on the structural design and synthesis of CTFs and their applications in CO catalysis including CO cycloaddition, CO carboxylation, CO hydrogenation, CO photoreduction, and CO electroreduction. By discussing the structure-property relationship, valuable guidance from a sustainable perspective may be provided for developing precisely designed CTFs with high performance and excellent industrial application prospects in sustainable CO catalysis.
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http://dx.doi.org/10.1002/cssc.202002422 | DOI Listing |
ChemSusChem
January 2025
Osaka University: Osaka Daigaku, Research Center for Solar Energy Chemistry, 1-3 Machikaneyama, Toyonaka, 560-8531, Osaka, JAPAN.
Electrochemically grown copper nanoclusters (CuNCs: < 3 nm) from single-atom catalysts have recently attracted intensive attention as electrocatalysts for CO2 and CO reduction reaction (CO2RR/CORR) because they exhibit distinct product selectivity compared with conventional Cu nanoparticles (typically larger than 10 nm). Herein, we conducted a detailed investigation into the size dependence of CuNCs on selectivity for multicarbon (C2+) production in CORR. These nanoclusters were electrochemically grown from single Cu atoms dispersed on covalent triazine frameworks (Cu-CTFs).
View Article and Find Full Text PDFAcc Chem Res
January 2025
School of Engineering, Westlake University, Hangzhou 310024, Zhejiang Province, China.
ConspectusCovalent triazine frameworks (CTFs) are a novel class of nitrogen-rich conjugated porous organic materials constructed by robust and functional triazine linkages, which possess unique structures and excellent physicochemical properties. They have demonstrated broad application prospects in gas/molecular adsorption and separation, catalysis, energy conversion and storage, etc. In particular, crystalline CTFs with well-defined periodic molecular network structures and regular pore channels can maximize the utilization of the features of CTFs and promote a deep understanding of the structure-property relationship.
View Article and Find Full Text PDFNano Lett
January 2025
Synergetic Extreme Condition High-Pressure Science Center, State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun 130012, China.
Covalent-organic frameworks (COFs) are dynamic covalent porous organic materials constructed from emissive molecular organic building blocks. However, most two-dimensional (2D) COFs are nonemissive or weakly emissive in the solid state owing to the intramolecular rotation and vibration together with strong π-π interactions. Herein, we report a pressure strategy to achieve the bright multicolor emission from yellow to red in the 2D triazine triphenyl imine COF (TTI-COF).
View Article and Find Full Text PDFSe Pu
February 2025
College of Chemical Engineering and Environment, China University of Petroleum-Beijing, Beijing 102249, China.
Trace contaminants are toxic and their widespread presence in the environment potentially threatens human health. The levels of these pollutants are often difficult to determine directly using instruments owing to the complexities of environment matrices. Hence, pretreatment steps, such as sample purification and concentration, are key along with various processes that enhance the accuracy and sensitivity of the detection method.
View Article and Find Full Text PDFJ Chromatogr A
January 2025
Faculty of Chemistry, Analytical Chemistry, University of Marburg, Hans-Meerwein-Str. 4, Marburg 35043, Germany. Electronic address:
Phosphonic acid cation exchange materials (PCX) are synthesized by atom transfer radical polymerization (ATRP) followed by alkyne-azide click-chemistry. ATRP is used to synthesize polymeric chains of diethyl 4-vinylbenzylphosphonate with different chain lengths, which are covalently bonded to the surface of monodisperse polystyrene-divinylbenzene (PS/DVB) particles by click-chemistry. The functionalized particles are characterized by FIB-SEM, IR and Schoeniger combustion followed by chromatographic experiments.
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