Metal nanoparticles are potent reaction catalysts, but they tend to aggregate, thereby limiting their catalytic efficiency. Their coordination with specific functional groups within a porous structure prevents their aggregation and facilitates the mass flow of catalytic starting materials and products. Herein, we use a thiacalix[4]arene-based polymer as a porous support with abundant docking sites for Au nanoparticles. The sulfur atoms bridging the phenolic subunits of thiacalix[4]arene serve as Lewis basic sites that coordinate Au atoms. Therefore, this approach takes advantage of the functional groups inherent in the monomer and avoids laborious postsynthetic modifications of the polymer. The presented system was tested for visible-light-driven photocatalytic CO reduction, where it showed adequate ability to generate 6.74 μmol g CO over the course of 4 h, while producing small amounts of the CH product. This study aims to stimulate interest in the design and development of synthetically simpler porous polymer supports for various metal nanoparticles in catalytic and other applications.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284511PMC
http://dx.doi.org/10.1021/acsami.2c05606DOI Listing

Publication Analysis

Top Keywords

visible-light-driven photocatalytic
8
photocatalytic reduction
8
metal nanoparticles
8
functional groups
8
polythiacalixarene-embedded gold
4
nanoparticles
4
gold nanoparticles
4
nanoparticles visible-light-driven
4
reduction metal
4
nanoparticles potent
4

Similar Publications

The development of efficient and sustainable photocatalysts for wastewater treatment remains a critical challenge in environmental remediation. In this study, a ternary photocatalyst, Cu-CuO/g-CN, was synthesized by embedding copper-copper oxide heterostructural nanocrystals onto g-CN nanosheets via a simple deposition method. Structural and optical characterization confirmed the successful formation of the heterostructure, which combines the narrow bandgap of CuO, the high stability of g-CN, and the surface plasmon resonance (SPR) effect of Cu nanoparticles.

View Article and Find Full Text PDF

Graphitic Carbon Nitride for Photocatalytic Hydrogen Production from Water Splitting: Nano-Morphological Control and Electronic Band Tailoring.

Nanomaterials (Basel)

December 2024

State Key Laboratory of Solidifcation Processing, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an 710072, China.

Semiconductor polymeric graphitic carbon nitride (g-CN) photocatalysts have garnered significant and rapidly increasing interest in the realm of visible light-driven hydrogen evolution reactions. This interest stems from their straightforward synthesis, ease of functionalization, appealing electronic band structure, high physicochemical and thermal stability, and robust photocatalytic activity. This review starts with the basic principle of photocatalysis and the development history, synthetic strategy, and structural properties of g-CN materials, followed by the rational design and engineering of g-CN from the perspectives of nano-morphological control and electronic band tailoring.

View Article and Find Full Text PDF

Carbon dots (CDs) mediated g-CN (CN) is a promising visible-light-driven semiconductor in catalyzing peroxymonosulfate (PMS) for aqueous contaminants remediation. However, the poor dispersibility of powered catalyst and its challenging recyclability impede their broader application. Herein, we embedded FeN bridge within the g-CN framework and immobilized g-CN gel beads (CA/FNCCN) through a 3D cross-linking process with sodium alginate.

View Article and Find Full Text PDF

Linkage Regulation of β-Ketoamine Covalent Organic Frameworks for Boosting Photocatalytic Overall Water Splitting.

ACS Appl Mater Interfaces

January 2025

Centre for Advanced Optoelectronic Functional Materials Research, Key Laboratory of UV-Emitting Materials and Technology, Ministry of Education, Northeast Normal University, Changchun 130024, China.

Two dimensional β-ketoamine covalent organic frameworks (2D TP-COFs) are one category of promising metal-free catalysts for photocatalytic overall water splitting (OWS) because of their unusual stability and versatile electronic/optical properties. However, none of the currently reported TP-COFs can accomplish the hydrogen evolution (HER) and oxygen evolution reactions (OER) simultaneously without adding any sacrificial agents and cocatalysts. To address this challenging issue, we rationally designed 23 2D TP-COFs by regulating the linkage groups and comprehensively evaluated their OWS activity by using the first-principles method.

View Article and Find Full Text PDF

A highly versatile Z-scheme heterostructure, HoSmSbO/YbDyBiNbO (HYO), was synthesized using an ultrasonic-assisted solvent thermal method. The HYO heterojunction, composed of dual ABO compounds, exhibits superior separation of photogenerated carriers due to its efficient Z-scheme mechanism. The synergistic properties of HoSmSbO and YbDyBiNbO, particularly the excellent visible light absorption, enable HYO to achieve exceptional photocatalytic performance in the degradation of fenitrothion (FNT).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!