Solar photocatalytic hydrogen production and photoelectrochmical behavior of self-prepared titanium dioxide modified with different precious metals
Yamen AlSalka a, Detlef W. Bahnemann a
a Institute of Technical Chemistry, Gottfried Wilhelm Leibniz University Hannover, DE, Callinstraße, 3, Hannover, Germany
b Laboratory “Photoactive Nanocomposite Materials” (Director), Saint-Petersburg State University, Ulyanovskaya str. 1, Peterhof, Saint-Petersburg, 198504
Materials for Sustainable Development Conference (MATSUS)
Proceedings of September Meeting 2016 (NFM16)
Berlin, Germany, 2016 September 5th - 13th
Organizers: Marin Alexe, Enrique Cánovas, Celso de Mello Donega, Ivan Infante, Thomas Kirchartz, Maksym Kovalenko, Federico Rosei, Lukas Schmidt-Mende, Laurens Siebbeles, Peter Strasser, Teodor K Todorov, Roel van de Krol and Ulrike Woggon
Poster, Yamen AlSalka, 065
Publication date: 14th June 2016

Shifting towards cleaner sources of energy needs great efforts to overcome the environmental problems of our modern society. Solar fuel and the use of solar energy for photocatalytic hydrogen production seem to be rather promising alternatives. Unfortunately, the lack of high efficient solar harvesting materials is the main obstacle towards the practical application. Titanium dioxide is considered to be one of the most widely used photocatalytic material despite the fact that it is only absorbs the UV light, hence its modification is requred in order to benefit of a wider range of solar spectrum.

Several self-prepared TiO2 photocatalyst has been synthesized via evaporation-induced self-assembly (EISA) method before its modification by precious metals using alloying and photodeposition methods. Au/TiO2 composite has been prepared by alloying method and its photocatalytic activity was compared with other composites prepared by Au loading on the surface of TiO2. Furthermore, photodeposition method has been used also to prepare Pt/TiO2 and Au-Pt/TiO2 composites.

All the self-prepared TiO2 photocatalysts and their composites with precious metals have been characterized by different techniques (XRD, DRS, TEM, and BET), and their flat-band potentials were determined using Mott-Schottky measurements.

It was found that in the presence of ethanol as a sacrificial agent and under solar light irradiation, the unmodified TiO2 photocatalyst achieved a maximum H2 evolution rate of 0.4 mmol.g-1.h-1 which was about 4 times higher than the evolution rate using P25 and UV100. Furthermore, the modification with gold enhanced the solar evolution of H2 and the results clearly showed that the photocatalytic activity of the employed photocatalysts seems to be dependent on the modification method, where a value of 5 and of 10.5 mmol.g-1.h-1 of H2 have been recorded. Moreover, loading Pt on the surface of TiO2 had a significant positive impact on the photocatalytic hydrogen evolution and their composites exhibited higher photocatalytic activity compared with that of Au/TiO2 composite. However, the presence of both Au and Pt nanoparticles did not have the expected high impact in raising the efficiency in solar light.

Finally, the impact of the modification of TiO2 by precious metals on the photoelectrochemical behavior was studied. A comparison of PEC catalytic activities was performed by linear sweep voltammetric scans, in dark and light, of several photoanodes prepared of the self-prepared composites. Also, the correlation between PEC measurements and the photocatalytic activity will be discussed.



© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info