Electrochemical Behavior of TiOxCy as Catalyst Support for Direct Ethanol Fuel Cells at Intermediate Temperature: From Planar Systems to Powders
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- 作者：Laura Calvillo ; Gonzalo García ; Andrea Paduano ; Olmedo Guillen-Villafuerte ; Carlos Valero-Vidal ; Andrea Vittadini ; Marco Bellini ; Alessandro Lavacchi ; Stefano Agnoli ; Alessandro Martucci ; Julia Kunze-Liebh?user ; Elena Pastor ; Gaetano Granozzi
- 刊名：ACS Applied Materials & Interfaces
- 出版年：2016
- 出版时间：January 13, 2016
- 年：2016
- 卷：8
- 期：1
- 页码：716-725
- 全文大小：559K
- ISSN：1944-8252
文摘
To achieve complete oxidation of ethanol (EOR) to CO2, higher operating temperatures (often called intermediate-T, 150–200 °C) and appropriate catalysts are required. We examine here titanium oxycarbide (hereafter TiOxCy) as a possible alternative to standard carbon-based supports to enhance the stability of the catalyst/support assembly at intermediate-T. To test this material as electrocatalyst support, a systematic study of its behavior under electrochemical conditions was carried out. To have a clear description of the chemical changes of TiOxCy induced by electrochemical polarization of the material, a special setup that allows the combination of X-ray photoelectron spectroscopy and electrochemical measurements was used. Subsequently, an electrochemical study was carried out on TiOxCy powders, both at room temperature and at 150 °C. The present study has revealed that TiOxCy is a sufficiently conductive material whose surface is passivated by a TiO2 film under working conditions, which prevents the full oxidation of the TiOxCy and can thus be considered a stable electrode material for EOR working conditions. This result has also been confirmed through density functional theory (DFT) calculations on a simplified model system. Furthermore, it has been experimentally observed that ethanol molecules adsorb on the TiOxCy surface, inhibiting its oxidation. This result has been confirmed by using in situ Fourier transform infrared spectroscopy (FTIRS). The adsorption of ethanol is expected to favor the EOR in the presence of suitable catalyst nanoparticles supported on TiOxCy.