Search Results (2)

Improving the efficiency of photocatalysts for hydrogen production while minimizing the amount of noble metals used is a pressing issue in modern green energy. This study examines the effect of ultra-small Pt additives on increasing the efficiency of the CuO_x-dark TiO₂ photocatalyst used in the hydrogen evolution reaction (HER). Initially, Pt was photoreduced from the hydroxonitrate complex (Me₄N)₂[Pt₂(OH)₂(NO₃)₈] onto the surface of nanodispersed CuO_x powder obtained by pulsed laser ablation. Then, the obtained Pt-CuO_x particles were dispersed on the surface of highly defective dark TiO₂, so that the mass content of Pt in the samples varied in the range from 1.25 × 10⁻⁵ to 10⁻⁴. The prepared samples were examined using HRTEM, XRD, XPS, and UV-Vis DRS methods. It has been established that in the Pt-CuO_x particles, platinum is mainly present in the form of single atoms (SAs), both as Pt²⁺ (predominantly) and Pt⁴⁺ species, which should facilitate electron transfer and contribute to the manifestation of the strong metal–support interaction (SMSI) effect between SA Ptⁿ⁺ and CuO_x. In turn, in the Pt-CuO_x-dark TiO₂ samples, surface defects (O_v) and surface OH groups on dark TiO₂ particles act as “anchors”, promoting the spontaneous dispersion of CuO_x in the form of sub-nanometer clusters with the reduction of Cu²⁺ to Cu¹⁺ when localized near such O_v defects. During photocatalytic HER in aqueous glycerol solutions, irradiation was found to initiate a large number of catalytically active Pt⁰-CuO_x-O_v-dark TiO₂ centers, where the SMSI effect causes electron transfer from titania to SA Pt, thus promoting better separation of photogenerated charges. As a result, ultra-small additives of Pt led to up to a 1.34-fold increase in the amount of released hydrogen, while the maximum apparent quantum yield (AQY) reached 65%. Full article

Cu-containing and Ce-modified OMS-2 catalysts were prepared at various calcination temperatures using the hydrothermal method and tested for low-temperature CO oxidation. The structure, chemical compositions, and physical–chemical properties of the catalysts were characterized using XRD, N₂ physisorption, XRF, Raman spectroscopy, SEM, high-resolution TEM with EDX, TPR-H₂, and XPS. The incorporation of Cu into the Ce-OMS-2 sample facilitated the transformation of pyrolusite into cryptomelane, as confirmed by Raman spectroscopy data. In the light-off mode, the Cu/Ce-OMS-2-300 and Cu/OMS-2 samples exhibited higher activity in low-temperature CO oxidation (T₉₀ = 115 and 121 °C, respectively) compared to sample Cu/Ce-OMS-2-450. After a long-run stability test, the Cu/Ce-OMS-X samples demonstrated excellent performance: the T₈₀ increased by 16% and 7% for the samples calcined at 300 °C and 450 °C, respectively, while the T₈₀ for the Cu/OMS-2 increased by 40%. The Cu/OMS-2 and Cu/Ce-OMS-2-300 samples were found to have an increased content of nanodispersed copper sites on their surfaces. These copper sites contributed to the formation of the Cu²⁺-O-Mn⁴⁺ interface, which is responsible for the CO oxidation. The presence of Ce³⁺ in the catalyst was found to increase its stability in the presence of water vapor due to the higher reoxidation ability in comparison with Ce-free sample Cu/OMS-2. Full article