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Proton-conducting materials are essential to the emerging hydrogen economy. Covalent triazine frameworks (CTFs) are promising proton-conducting materials at high temperatures but need more effective sites to strengthen interaction for proton carriers. However, their construction and design in a concise condition are still challenges. Herein, we show a low temperature approach to synthesize CTFs via a direct cyclotrimerization of aromatic aldehyde using ammonium iodide as facile nitrogen source. Among the CTFs, the perfluorinated CTF (CTF-TF) was successfully synthesized with much lower temperature ( ≤ 160 °C) and open-air atmosphere. Due to the additional hydrogen-bonding interaction between fluorine atoms and proton carriers (HPO), the CTF-TF achieves a proton conductivity of 1.82 × 10S cm at 150 °C after HPO loading. Moreover, the CTF-TF can be readily integrated into mixed matrix membranes, displaying high proton conduction abilities and good mechanical strength. This work provides an alternative strategy for rational design of proton conducting media.
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http://dx.doi.org/10.1038/s41467-023-43829-4 | DOI Listing |
J Colloid Interface Sci
August 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, PR China; Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt. Electronic address:
Post-synthetic modification (PSM) offers a promising approach for tailoring the compositional, structural, and electronic properties of covalent organic frameworks (COFs), thereby enhancing their exciton dissociation ability and facilitating charge transfer. The effectiveness of these approaches is largely compromised by the harsh conditions, complexity, and alteration of the original structure. Therefore, developing a facile yet effective PSM for modulating COFs' properties without altering the original geometry and/or structure is a challenge.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.
Electrochemical CO reduction (COR) with transition-metal catalysts often suffers from low selectivity for value-added products. Organic layers have been explored to enhance selectivity by modifying local environments and adjusting the CO and CO adsorption, but their role remains unclear due to structural and mechanical instability. Here, we designed a well-defined organic layer model consisting of ∼4 nm-thick covalent organic framework (COF) films with ∼3 nm pores and a cm-scale area.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
School of Energy and Environment, Southeast University, Nanjing, 211189, China.
Two-dimensional covalent organic frameworks (2D COFs) have emerged as promising photocatalysts due to their high surface areas and precisely tunable physicochemical properties. However, it remains a significant challenge to precisely control over interlayer stacking configurations in 2D COFs, which critically influence charge carrier transport and consequently determine catalytic efficiency. In this study, we demonstrate a solvent-driven strategy to precisely regulate the interlayer stacking configurations of metal-incorporated 2D COFs, successfully achieving both AA eclipsed (COF-TD-AA) and ABC staggered (COF-TD-ABC) configurations.
View Article and Find Full Text PDFAdv Mater
August 2025
School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.
The continuing increase in atmospheric carbon dioxide (CO), a major greenhouse gas and accelerating climate change are driving demand for innovative mitigation strategies. The photocatalytic CO reduction reaction (PCORR) presents a promising and sustainable route to convert CO into useful hydrocarbons and fuels utilizing sunlight, thereby mitigating CO emissions. This review examines the developmental aspects of light-driven CO conversion using organic polymeric photocatalysts, focusing on carbon nitrides (CNs), covalent triazine frameworks (CTFs), and covalent organic frameworks (COFs).
View Article and Find Full Text PDFRSC Adv
August 2025
Manipal Technologies Limited Manipal 576104 Karnataka India.
A hierarchical hybrid material (MnO@COP) with dual charge storage capabilities was created by synthesizing a triazine-based covalent organic polymer (COP) that is rich in nitrogen functionalities and integrating it with MnO nanoparticles. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), Brunauer-Emmett-Teller (BET) studies, and X-ray photoelectron spectroscopy (XPS) demonstrated a distinct architecture: MnO nanoparticles were uniformly embedded in a stable, porous COP matrix. MnO loading caused a modest decrease in surface area, but the composite still had the mesoporosity needed for quick ion diffusion.
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