For dye-sensitized solar cell (DSSC), an efficient transport of electron from the dye sensitizer through the mesoporous
oxide layer and to be collected by electrode is crucial for high photovoltaic conversion efficiency. In this work, two
novel approaches were developed in DSSC fabrication to improve the overall photovoltaic performance. The concurrent
improvement in the charge transport property and light harvesting efficiency was achieved by incorporating N-doped
TiO2 in the mesoporous TiO2 layer of the photoanode. These N-doped TiO2 (TiNxOy) was formed by using the single step thermal oxidation of Titanium Nitride (TiN) nanomaterials. At the same time, the 3D electrode with SnO2 nanorods grown on the FTO glass using plasma enhanced chemical vapor deposition (PECVD) system was used to enhance the charge collection efficiency. By combining these two approaches simultaneously, the DSSC with composite TiNxOy-TiO2 photoanode on SnO2 nanorods 3D electrode was successfully fabricated and characterized. As compared to the standard DSSC, an overall increment of 28 % in the conversion efficiency was achieved. Higher incident photon-current conversion efficiency (IPCE) values were also obtained, specifically for the region 400 – 500 nm due to the cosensitization effect of N-doped TiO2. Efficient transfer of electron due to the decrease in charge transfer resistance at the mesoporous oxide/dye/electrolyte interface was observed from electrochemical impedance spectroscopy (EIS) measurement. With the use of SnO2 nanorods, the adhesion between the mesoporous TiO2/FTO was enhanced and the transit time of a photogenerated electron through the mesoporous layer before being collected at the FTO electrode was significantly reduced by 50 %.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.