Bare zinc oxide (ZnO) and Ba-doped ZnO (BZO) samples were prepared by using a simple precipitation method. The effects of Barium doping on the structural, morphological, and optoelectronic properties, as well as on the physico-chemical features of the surface were investigated and correlated with the observed photocatalytic activity under natural solar irradiation. The incorporation of Ba ions into the ZnO structure increased the surface area by ca. 14 times and enhanced the hydrophilicity with respect to the bare sample, as demonstrated by infrared spectroscopy and contact angle measurements. The surface hydrophilicity was correlated with the enhanced defectivity of the doped sample, as indicated by X-ray diffraction, Raman, and fluorescence spectroscopies. The resulting higher affinity with water was, for the first time, invoked as an important factor justifying the superior photocatalytic performance of BZO compared to the undoped one, in addition to the slightly higher separation of the photoproduced pairs, an effect that has already been reported in literature. In particular, observed kinetic constants values of 8∙10 and 11.3∙10 min were determined for the ZnO and BZO samples, respectively, by assuming first order kinetics. Importantly, Ba doping suppressed photocorrosion and increased the stability of the BZO sample under irradiation, making it a promising photocatalyst for the abatement of toxic species.
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http://dx.doi.org/10.3390/nano13202742 | DOI Listing |
Dalton Trans
January 2025
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, P. R. China.
Efficient separation of photogenerated charge carriers is essential for maximizing the photocatalytic efficiency of semiconductor materials in oxygen evolution reactions (OER). This study presents a novel trimetallic photocatalyst, MIL-100(Fe)/TiO/CoO, synthesized through a facile microwave-assisted hydrothermal method followed by atomic layer deposition (ALD). The porous MIL-100(Fe) serves as a support for the sequential deposition of TiO and CoO layers ALD, which enhances electron-hole pair separation and minimizes their recombination.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Fujian Provincial Key Laboratory of Polymer Materials, College of Materials Science and Engineering, Fujian Normal University, Fuzhou 350007, China.
In this study, the NiFe-LDH doped with different Pt group metals (Pt, Ru, Ir, Rh) was prepared as a cocatalyst for photocatalytic H production over g-CN. It is found that the doped NiFe-LDH loaded g-CN generally displays higher photocatalytic activity than the raw NiFe-LDH modified one, where the NiFeRu-LDH loaded g-CN shows the optimal H evolution rate of 77.4 μmol h, about 5.
View Article and Find Full Text PDFNat Commun
January 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, PR China.
The H-evolution kinetics play a pivotal role in governing the photocatalytic hydrogen-evolution process. However, achieving precise regulation of the H-adsorption and H-desorption equilibrium (H/H) still remains a great challenge. Herein, we propose a fine-tuning d-p hybridization strategy to precisely optimize the H/H kinetics in a Ni-B modified CdS photocatalyst (Ni-B/CdS).
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Environmental and Chemical Engineering, Jiangsu Ocean University, Lianyungang 222000, PR China. Electronic address:
Metal-organic frameworks (MOFs) have shown significant potential in the photocatalytic activation of peroxydisulfate (PDS). Although many MOFs have been investigated for their ability to activate PDS, the impact of structural interpenetration on this process remains underexplored. In this study, MIL-88D(FeNi) and MIL-126(FeNi) were selected to systematically study this effect.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Analysis and Testing Center, Xinyang University, Xinyang 464000 China. Electronic address:
A significant enhancement in the photocatalytic activity of metal-organic frameworks (MOFs) is achieved by expanding the visible-light response range through the strategic incorporation of functional groups, such as metalloporphyrins. Herein, Pd-metalised tetrakis(4-carboxyphenyl)porphyrin (PdTCPP) photosensitiser is integrated into the UiO-66-(NH) framework, creating the hybrid material PdTCPP ⊂ UiO-66-(NH) using a facile mixed-ligand strategy. Platinum nanoparticles (Pt NPs) are subsequently introduced as a co-catalyst via in situ photoreduction, resulting in the formation of the Pt/PdTCPP ⊂ UiO-66-(NH) hybrid material, which demonstrates exceptional catalytic performance under visible-light irradiation.
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