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Recently, low-cost graphitic carbon nitride (g-C3N4) revealed high photocatalytic activities and provided solutions to environmental pollution. In this study, we synthesized brown mesoporous 2D g-C3N4 by calcination dicyandiamide with pluronic P123. This is followed by loading of Ag NPs on the prepared 2D g-C3N4 by photodeposition process. After that, a ternary composite 2% Ag/ 2D g-C3N4 / g-C3N4 QDs heterojunction photocatalyst has been successfully prepared. The prepared nanomaterials were comprehensively characterized by various analysis techniques such as XRD, UV–Vis., BET, XPS, SEM, TEM. This new system exhibited a large surface area with porous structure and a wide absorption of visible light. The results verified that Ag NPs decoration enhanced the charge separation of photo-generated carriers of g-C3N4 2D and g-C3N4 QDs, promote significant enhancement in the photocatalytic activity for reduction of p-nitrophenol with a rate constant (k) value of 0.49729 / min in 6 min. This rate is about two-fold higher than that observed for pure g-C3N4 2D and g-C3N4 QDs as well as shows an improvement compared to 2% Ag/ g-C3N4 2D and g-C3N4 2D/ g-C3N4 QDs. The results open the door to design highly efficient 2D/0D nanocomposite photocatalysts for a wide variety of environmental applications. [ABSTRACT FROM AUTHOR]

4-Nitrophenol (4-NP) is reported to originate disadvantageous effects on the human body collected from industrial pollutants; therefore, the detoxification of 4-NP in aqueous contamination is strongly recommended. In this study, the heterojunction mesoporous α-Fe2O3/TiO2 modulated with diverse Ag percentages has been constructed via a sol–gel route in the occurrence of a soft template P123. The formation of biphasic crystalline TiO2 anatase and brookite phases has been successfully achieved with the average 10 nm particle sizes. The photo/-catalytic reduction of 4-NP has been performed utilizing NaBH4 as a reducing agent with and without visible illumination. All Ag/Fe2O3/TiO2 nanocomposites exhibited significantly higher photo/-catalytic reduction efficiency than pure Fe2O3, TiO2 NPs, and Fe2O3/TiO2 nanocomposite. 2.5% Ag/Fe2O3/TiO2 nanocomposite was considered the highest and superior photocatalytic reduction efficiency, and it almost achieved 98% after 9 min. Interestingly, the photocatalytic reduction of 4-NP was accelerated 9 times higher than the catalytic reduction over 2.5% Ag/Fe2O3/TiO2; its rate constant value was 709 and 706 times larger than pure TiO2 and Fe2O3 NPs, respectively. The enhanced photocatalytic reduction ability of Ag/Fe2O3/TiO2 nanocomposite might be referred to as significantly providing visible light absorption and a large surface area, and it can upgrade the effective separation and mobility of electron holes. The stability of the synthesized catalysts exhibited that the obtained catalysts can undergo a slight decrease in reduction efficiency after five successive cycles. This approach highlights a novel route for constructing ternary nanocomposite systems with high photo/-catalytic ability. [ABSTRACT FROM AUTHOR]

The synthesis and stabilization of Pd nanoclusters on a support, as well as simultaneously achieving optimal catalytic activity, remain challenging tasks. Functionalizing the support surface with specific ligands offers a promising solution, but it often requires carefully balancing trade-offs between the reaction yield and catalyst stability. Here, we used two different ligands (propylamine and propylthiol) to functionalize the layered silicate's interlayer surface for Pd nanocluster synthesis and stabilization. For dehydrogenating formic acid, Pd nanoclusters on aminopropyl groups achieved a catalytic activity ∼27-fold higher than that of thiopropyl groups at 70 °C. Our density functional calculations compared the adsorption energetics and bonding characteristics of single Pd atoms and Pd 13 nanoclusters on amino- and thio-functionalized silicate surfaces. Pd-N bonds were predicted to be weaker with minimal covalency, while Pd-S bonds exhibit greater covalency due to higher 4d-3p hybridization, resulting in better stability. However, Pd 13 clusters undergo severe structural deformation on thiol-functionalized surfaces, resulting in a smaller overall surface area and diminished catalytic stability.