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P Reñones, A Moya, F Fresno, L Collado, JJ Vilatela

In this research work, the gas phase CO2 photocatalytic reduction using water as electron donor has been performed using hierarchical assemblies of mesoporous TiO2 1-D nanofibres synthesised by a combination of electrospinning and sol–gel methods. In order to compare the effect of the crystallisation step on oxygen vacancies and conductivity, two different annealing conditions have been undertaken: under a high Ar flow (“TiO2 Fibres-A” sample) and under static Ar (“TiO2 Fibres B” sample). Moreover, these materials have been compared with individualised TiO2 nanoparticles prepared by a sol-gel procedure. CO and H2 are detected as major products with all photocatalysts, with lower amounts of CH4 and CH3OH. The TiO2 nanofibres exhibit better results than the sol-gel photocatalyst, behaviour that may be ascribed to an improved nanocrystals connection, which favours a fast charge transport along the grain boundaries, as measured by electrochemical impedance spectroscopy (EIS). The highest CO2 reduction activity is achieved with the TiO2 Fibres B catalyst, which gives rise to ca. 4 and 2.5 times higher H2 and CO production, respectively, than the TiO2 Fibres-A one. This sample is composed of a mixture of anatase and rutile crystalline phases (80:20), leading to a decrease in the electron-hole recombination rate observed by photoluminescence (PL) measurements.
Photoluminescence spectra of fibre and sol-gel catalysts

(1), considering the number of electrons required to obtain each product, and measuring the incident spectral irradiance on the surface of the catalyst below 400nm by means of an optical fibre StellarNet UVNb-50 spectrometer.

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