The loading of cocatalysts is an effective approach to optimize the separation of carriers during photocatalytic processes. Among them, cocatalysts often work independently during the photocatalytic production of H. However, an investigation of the synergistic effect of dual cocatalysts is beneficial for further promoting photocatalytic H production activity. In this work, dual cocatalyst NiP-NiS-modified TiO nanosheets were fabricated through a solvent evaporation method. The investigation indicates that NiP-NiS can widen the light absorption range and reduce the contact angle between TiO and water from 26.71 to 8.27°, which facilitates the adsorption of water molecules. Besides, the introduction of NiP-NiS can decrease the overpotential of H evolution and induce more electrochemically active surface area. The photocatalytic tests show that the H production rate of 15% NiP-NiS/TiO can reach up to 4891.6 μmol·g·h, which is 30.2, 4.4, and 1.3 times than pure TiO (161.8 μmol·g·h), 15% NiP/TiO (1112.1 μmol·g·h), and 15% NiS/TiO (3678.1 μmol·g·h), respectively. The enhancement mechanism of photocatalytic H production is attributed to the Schottky barrier effect between NiP-NiS nanoparticles and TiO nanosheets, which can enormously promote the interface charge separation and transfer, and enhance the kinetics of H production. This work provides a potential strategy for enhancement H production using appropriate dual cocatalyst-decorated semiconductor materials.
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http://dx.doi.org/10.1021/acs.langmuir.3c02719 | DOI Listing |
Mol Divers
January 2025
School of Life Sciences, Jilin University, 2699 Qianjin Street, Changchun, 130012, People's Republic of China.
The 2-substituted benzimidazole has emerged as a promising heterocyclic compound in the field of drug design. In pursuit of more sustainable photocatalysts for 2-substituted benzimidazole synthesis, the method for coating FeO with V-doped TiO was presented. On the base of characterizing composition, morphology, and properties, the prepared nano-sized FeO@V/TiO composites were used as a heterogeneous photocatalyst to catalyze the synthesis of 2-substituted benzimidazoles under light.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Physics, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jalan Ganesha 10, Bandung, West Java 40132, Indonesia.
Bismuth oxychloride (BiOCl) is known for its unique layered microstructure, which plays a pivotal role in enhancing its photocatalytic properties. This study introduces a novel strategy for controlling the phase composition, facet orientation, and oxygen vacancy formation in BiOCl through precise pH adjustment during the synthesis. By employing a hydrothermal method, we systematically varied the pH to produce distinct BiOCl phases and conducted detailed structural and photocatalytic analyses.
View Article and Find Full Text PDFRSC Adv
January 2025
School of Chemistry and Molecular Engineering, East China University of Science and Technology 130 Meilong Road Shanghai 200237 China.
The hydrogenation of carbon dioxide into profitable chemicals is a viable path toward achieving the objective of carbon neutrality. However, the typical approach for hydrogenation of CO heavily relies on thermally driven catalysis at high temperatures, which is not aligned with the goals of carbon neutrality. Thus, there is a critical need to explore new catalytic methods for the high-efficiency conversion of CO.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, 117585, Singapore, Singapore.
Photocatalytic conversion has emerged as a promising strategy for harnessing renewable solar energy in the valorization of plastic waste. However, research on the photocatalytic transformation of plastics into valuable nitrogen-containing chemicals remains limited. In this study, we present a visible-light-driven pathway for the conversion of polylactic acid (PLA) into alanine under mild conditions.
View Article and Find Full Text PDFNature
January 2025
Department of Chemical Engineering, University College London, London, UK.
Methane, the major component of natural and shale gas, is a significant carbon source for chemical synthesis. The direct partial oxidation of methane to liquid oxygenates under mild conditions is an attractive pathway, but the molecule's inertness makes it challenging to achieve simultaneously high conversion and high selectivity towards a single target product. This difficulty is amplified when aiming for more valuable products that require C-C coupling.
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