Published February 10, 2016 | Version v1
Journal article

Interfacial modification of TiO2 nanoparticles by using carbonates of earth alkali metals as an efficient and simple approach for improving quantum dot sensitized solar cell performance

Description

In this paper, we investigate the effect of interfacial modification of TiO2 photoelectrodes with insoluble carbonates of earth alkali metals on the suppression of electron recombination and the photovoltaic performance of the Quantum dot-sensitized solar cells (QDSSCs). This layer can form an energy barrier at the electrode/electrolyte interface that leads to a better electron injection and increases electron accumulation in the TiO2 layer. The highest efficiency is achieved by applying TiO2/CaCO3/QDs layers that efficiency improves from 2.36% to 3.38% in the modified system and corresponding to 43% efficiency increment compared to bare TiO2 based QDSSCs under standard air mass 1.5 global (AM 1.5G) simulated sun light. The higher efficiency results from an increase in the values of Jsc and Voc, which is related to the improved electron transfer properties and decrease in the electron recombination in the QDSSCs. To find further evidence of the correlation between the effect of insulating layer and the suppression of back electron process and electron transfer rate, electrochemical impedance analyses (EIS) and the intensity modulated photocurrent/voltage spectroscopy (IMPS/IMVS) studies are performed under standard conditions. The results of this study show that this simple modification can significantly improve the performance of QDSSCs.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2016.01.152

Additional details

Identifiers

DOI
10.1016/j.electacta.2016.01.152;
PII
S0013-4686(16)30154-2;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
191
Journal Page Range
p. 987-995
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.