98%
921
2 minutes
20
Developing a facile method to overcome the intrinsic shortcomings of g-CN photocatalyst concerning its insufficient visible light absorption and dissatisfactory separation efficiency of charge carriers is of great significance but remains a challenge. In this work, we report, for the first time, a sapiential strategy for preparing highly efficient nitrogen-deficient g-CN featuring bunchy microtubes [R-tubular carbon nitride (TCN)] via a KOH-assisted hydrothermal treatment of rodlike melamine-cyanuric acid (RMCA) supramolecular aggregates followed by heating the reconstructed RMCA, in which KOH serves as an all-rounder for breaking hydrogen bonds, accelerating hydrolysis of melamine and nitrogen defects forming. This approach endows R-TCN with unique bunchy microtube morphology, enriched nitrogen defects, textural properties, and electronic structure, which result in narrower band gap, higher electric conductivity, more active sites, more negative conductive band, significantly increased visible light harvesting capability, and improved separation efficiency of charge carriers. As a consequence, R-TCN shows 2.44 and 39 times higher hydrogen evolution rate (8.19 μmol h) than that of the pristine TCN from RMCA and bulk g-CN from melamine. This new discovery may open a new avenue to fabricate highly efficient g-CN catalysts.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.8b04227 | DOI Listing |
Small
September 2025
School of Chemistry and Chemical Engineering, Key Lab of Fuel Cell Technology of Guangdong Province, South China University of Technology, Guangzhou, 510641, China.
Aggregation-induced electrochemiluminescence (AIECL) is a promising strategy for enhancing electrochemiluminescence (ECL) efficiency by minimizing energy loss of excited-state ECL emitters. However, rational design of high-efficiency AIECL emitters is hindered by limited mechanistic understanding and an unclear structure-performance relationship. To address this, four supramolecular coordination frameworks (SCFs) with varying π-bridge structures are synthesized using pyridine-functionalized tetraphenylethene (TPE) as the ligand and Pt(II) as the coordination center.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
Cyclic peptides (CPs) are versatile building blocks whose conformational constraints foster ordered supramolecular architectures with potential in biomedicine, nanoelectronics, and catalysis. Herein, we report the development of biomimetic antifreeze materials by conjugating CPs bearing ice-binding residues to 4-arm polyethylene glycol (PEG) via click chemistry. The concentration-dependent self-assembly of these CP-PEG conjugates induces programmable morphological transitions, forming nanotube networks above the critical aggregation concentration (CAC) and two-dimensional nanosheet networks near the CAC.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
Department of Chemistry, Bahir Dar University, PO Box 79, Bahir Dar, Ethiopia.
The title compound, CHNO·Br·CBr, consists of one 4-formyl-,-di-methyl-benzenaminium bromide and a tetra-bromo-methane mol-ecule. In the crystal, the bromide ions link 4-formyl-,-di-methyl-benzenaminium moieties through inter-molecular C-H⋯Br and N-H⋯Br hydrogen bonds, while inter-molecular C-H⋯O hydrogen bonds link 4-formyl-,-di-methyl-benzenaminium cations, enclosing (18) ring motifs, into a di-periodic network structure. The tetra-bromo-methane mol-ecules fill the spaces between the layers.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
School of Materials Science and Engineering, Beijing Institute of Technology, 100081 Beijing, China. Electronic address:
Nanozymes are nanomaterials designed to mimic the catalytic functions of natural enzymes, offering advantages such as enhanced stability, tunability, and scalability. Although precise control over the spatial arrangement of catalytic centers is essential for maximizing nanozyme activity, it remains a fundamental challenge in nanozyme design. Here, we present a supramolecular strategy to achieve molecular-level engineering of catalytic centers by grafting hemin onto monodisperse cellulose oligomers (MCOs).
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
State Key Laboratory of Advanced Materials for Intelligent Sensing and Key Laboratory of Organic Integrated Circuits, Ministry of Education & Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Institute of Molecular Plus, Department of Chemistry, Tianjin University, Tianjin 300072, China.
Incorporating boron atoms into organic macrocycles imparts unique chemical, electronic, and optical properties. The concept of making use of dative boron-nitrogen (B ← N) bonds for the construction of macrocycles has been proposed, but very few examples have been prepared with functional structures, much less pillar-like and other prismatic macrocycles, and their various functionalities have not been fully exploited. Here, we introduce a "functional molecular wall" synthetic protocol based on the self-assembly characteristics of B ← N dative bonds to construct highly symmetrical macrocycles, forming a quasi-pentagonal-shaped macrocycle (named [5]pyBN-) with a pillar-like structure.
View Article and Find Full Text PDF