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V.A. de la Peña O'Shea

Researcher at Energy Institute

Publications -  9
Citations -  375

V.A. de la Peña O'Shea is an academic researcher from Energy Institute. The author has contributed to research in topics: Photocatalysis & Catalysis. The author has an hindex of 7, co-authored 9 publications receiving 286 citations.

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Effect of Au surface plasmon nanoparticles on the selective CO2 photoreduction to CH4

TL;DR: In this article, the photocatalytic activity of gold-supported TiO2 catalysts was evaluated in the gas phase while using H2O as electron donor and UV and visible light as energy sources.
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CO2 reduction over NaNbO3 and NaTaO3 perovskite photocatalysts

TL;DR: Both catalysts exhibit interesting intrinsic activities, with the tantalate material giving rise to a slightly higher performance, attributed to a compromise situation between electron-hole recombination and the reducing potential of conduction band electrons.
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Enhancement of hydrocarbon production via artificial photosynthesis due to synergetic effect of Ag supported on TiO2 and ZnO semiconductors

TL;DR: In this paper, the effect of silver on the catalytic activity of Ag/TiO 2 and Ag/ZnO systems for the CO 2 photoreduction using water vapour as electron donor has been investigated.
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Photocatalytic hydrogen production in the water/methanol system using Pt/RE:NaTaO3 (RE = Y, La, Ce, Yb) catalysts

TL;DR: In this paper, a perovskite type RE-doped NaTaO3 (where RE represents Rare Earths elements like Y, La, Ce, Yb) catalysts, derived from solid state synthesis method, have been used for the photocatalytic hydrogen production from water using methanol as sacrificial agent.
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Mild temperature hydrogen production by methane decomposition over cobalt catalysts prepared with different precipitating agents

TL;DR: In this paper, the physicochemical properties of the catalysts precursors vary with the precipitating agent, which shows a significant influence in their catalytic performance, and it is worth mentioning that the catalyst prepared using Na2CO3 shows significant activity in this reaction even at temperatures as low as 400°C.