Covalent organic framework nanosheets (COF NSs or CONs), as compared to their bulk counterparts two-dimensional (2D) covalent organic frameworks (COFs), exhibit superior performance in many aspects due to their fully accessible active sites benefiting from their ultrathin porous 2D structures. The development of a scalable synthetic methodology for CONs is crucial to further exploration of their unique properties and practical applications. Herein, we report an efficient strategy to fabricate ultrathin CONs through direct polycondensation of monomers under ultrasonic treatment and mild conditions. This method is facile and scalable, which is demonstrated by gram-scale synthesis of two ultrathin 2D CONs in several hours. Moreover, the as-prepared ultrathin CONs show excellent heterogeneous photocatalytic performance for the degradation of organic pollutants (dyes as representatives), remarkably superior to the bulk COFs prepared from the corresponding monomers under solvothermal conditions. This research provides a new roadmap for the scalable and facile synthesis of ultrathin CONs, which is of paramount importance for fully exploring the tremendous potential of this emerging type of 2D material.
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http://dx.doi.org/10.1039/d1sc05504f | DOI Listing |
ACS Appl Mater Interfaces
September 2024
College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji, Shaanxi 721013, P. R. China.
J Colloid Interface Sci
October 2024
CAS Key Laboratory of Urban Pollutant Conversion, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China; CAS Key Laboratory of Urban Pollutant Conversion, Department of Environmental Science and Technology, University of Science and Technology of China, Hefei 230026, China. Electronic address:
Anal Chim Acta
March 2024
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China. Electronic address:
Enhancing electrochemiluminescence (ECL) properties of luminophores is a hot direction in the current ECL field. Herein, we found that covalent rigidification of the aggregation-induced emission luminogens (AIEgens) TABE (TABE = tetra-(4-aldehyde-(1,1-biphenyl))ethylene) into covalent organic framework nanosheets (TABE-PZ-CON, PZ = piperazine) could result in stronger ECL emission than those of TABE aggregates and TABE monomers. We termed the interesting phenomenon "covalent rigidification-triggered electrochemiluminescence (CRT-ECL) enhancement".
View Article and Find Full Text PDFAdv Mater
April 2024
Department of Chemistry and State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong, 999077, China.
Metalloporphyrins and metallophthalocyanines emerge as popular building blocks to develop covalent organic nanosheets (CONs) for CO reduction reaction (CORR). However, existing CONs predominantly yield CO, posing a challenge in achieving efficient methanol production through multielectron reduction. Here, ultrathin, cationic, and cobalt-phthalocyanine-based CONs (iminium-CONs) are reported for electrochemical CO-to-CHOH conversion.
View Article and Find Full Text PDFDalton Trans
August 2023
Inorganic Membranes, Department of Science and Technology and MESA+ Institute for Nanotechnology, University of Twente, PO Box 217, 7500 AE Enschede, The Netherlands.
Atomic layer deposition (ALD) is a widely recognized technique for depositing ultrathin conformal films with excellent thickness control at Ångström or (sub)monolayer level. Atmospheric-pressure ALD is an upcoming ALD process with a potentially lower ownership cost of the reactor. In this review, we provide a comprehensive overview of the recent applications and development of ALD approaches emphasizing those based on operation at atmospheric pressure.
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