Please use this identifier to cite or link to this item:
|Title:||Photocatalytic-thermal water splitting||Authors:||Ernest, C.K.J.
|Issue Date:||2013||Citation:||Ernest, C.K.J.,Goh, T. (2013). Photocatalytic-thermal water splitting. 2013 International Conference on Electronics, Computers and Artificial Intelligence, ECAI 2013 : -. ScholarBank@NUS Repository. https://doi.org/10.1109/ECAI.2013.6636213||Abstract:||The concept of using solar energy to drive the conversion of water into hydrogen and oxygen has been examined in this work. One of the primary objectives of this work is to study the impact of thermal energy on the effectiveness of photocatalytic water splitting rate. Two types of photocatalyts, Ga2O3-Zn and TiO2-Pt, were employed for this present study. The effects of several process parameters on the photocatalytic production of hydrogen were also investigated. The parameters are, namely, the different variants of TiO2 catalysts, the pH levels of the water solution, the concentration of methanol in the solution, the photocatalyst processing method and the catalytic reaction temperature. Reaction temperatures, spanning 48 to 96.5°C, were controlled via the introduction of the appropriate level of thermal energy. Key results showed that higher pH levels and alcoholic content of the water positively impact the production of hydrogen. Additionally, both photocatalysts, Ga2O3-Zn and TiO2-Pt, demonstrated positive impact on the overall water splitting reaction with increased reaction temperature. It was further shown that the water splitting rates increased monotonically with higher reaction temperature in the tested range of 56 to 88.5°C, and 48 to 96.5°C for the respective photocatalysts, Ga2O3-Zn and TiO2-Pt. © 2013 IEEE.||Source Title:||2013 International Conference on Electronics, Computers and Artificial Intelligence, ECAI 2013||URI:||http://scholarbank.nus.edu.sg/handle/10635/86053||DOI:||10.1109/ECAI.2013.6636213|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Nov 30, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.