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dc.contributor.authorHamad, Hesham
dc.contributor.authorBailón García, Esther 
dc.contributor.authorMaldonado Hodar, Francisco José 
dc.contributor.authorPérez Cadenas, Agustín Francisco 
dc.contributor.authorCarrasco Marín, Francisco 
dc.contributor.authorMorales Torres, Sergio 
dc.date.accessioned2025-01-29T12:03:43Z
dc.date.available2025-01-29T12:03:43Z
dc.date.issued2018-09-08
dc.identifier.citationAppl. Catal. B: Env. 241, 2019, 385.es_ES
dc.identifier.urihttps://hdl.handle.net/10481/100957
dc.description.abstractBlack TiO2 is capable to absorb the entire or part of the visible spectrum improving, a priori, the photoactivity under solar irradiation. Nevertheless, black TiO2 materials have not been able to demonstrate the expected photocatalytic activity in visible light due to the presence of a large number of recombination centers. In addition, high temperatures or pressures (>400 °C, 20 bar) are required for the conventional synthesis and alternative methods have high energy costs which limit the capability for mass production. In this report, a novel controlled hydrolysis method has been developed to synthesize reduced black TiO2 in mild conditions of temperature (180 °C) and pressure (8 bar). The synergetic effect of the stabilization of small crystal sizes, strong visible light absorption, band gap narrowing, Ti3+ defects or oxygen vacancies concentration, improved surface area and pollutant-surface interactions, significantly enhances the photocatalytic activity in the degradation of organic pollutants (Orange G) under visible light (almost totally degraded at 40 min).es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleSynthesis of TixOy nanocrystals in mild synthesis conditions for the degradation of pollutants under solar lightes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doihttps://doi.org/10.1016/j.apcatb.2018.09.016
dc.type.hasVersionAMes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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