4.7 Article Proceedings Paper

Hierarchical TiO2 nanofibres as photocatalyst for CO2 reduction: Influence of morphology and phase composition on catalytic activity

期刊

JOURNAL OF CO2 UTILIZATION
卷 15, 期 -, 页码 24-31

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jcou.2016.04.002

关键词

CO2 photoreduction; Artificial photosynthesis; Hierarchical TiO2 fibres; Electrospinning; Sol-gel

资金

  1. European Research Council (ERC) under the European Union's Horizon research and innovation programme [648319]
  2. Comunidadde Madrid [S2013/MIT-3007]
  3. European Union's Seventh Framework Programme (AMAROUT-II PEOPLE-COFUND Action, REA grant ) [291803]

向作者/读者索取更多资源

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 H-2 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 H-2 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. (C) 2016 The Authors. Published by Elsevier Ltd.

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