TY - JOUR
T1 - Enhanced light harvesting and charge recombination control with TiO2/PbCdS/CdS based quantum dot-sensitized solar cells
AU - Kim, Hee Je
AU - Xu, Guo Cheng
AU - Gopi, Chandu V.V.M.
AU - Seo, Hyunwoong
AU - Venkata-Haritha, Mallineni
AU - Shiratani, Masaharu
N1 - Funding Information:
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, ICT and Future planning (NRF-2016K2A9A2A08003717).
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Charge recombination is considered as one of the most significant factors in hindering the photovoltaic performance of quantum dot-sensitized solar cells (QDSSCs). In addition, expand the light absorption range to the near-infrared region in QDSSCs increasing the generated photocurrent. A significant enhancement in the power conversion efficiency (PCE) of QDSSCs has been obtained by charge recombination control and enhanced light harvesting. In this respect, PbCdS layer is introduced between TiO2 and CdS QDs via a facile successive ionic layer absorption and reaction (SILAR) method in order to further improve the cell performance. For the first time a photoanode assembly composed of TiO2/PbCdS/CdS was prepared in QDSSCs. The photovoltaic parameters were significantly enhanced with the incorporation of a PbCdS intermediate layer between TiO2 and CdS QDs but varied appreciably with the SILAR cycles of PbCdS. When four SILAR cycle layer was applied, the PCE is as high as 3.35%, which is higher than the efficiency of 1.84% for the solar cell without PbCdS layer. The improved performance of the TiO2/PbCdS/CdS-based QDSSCs was attributed to the PbCdS layer can enhance the light harvesting to release more excitons. In addition, the PbCdS layer accelerates the electron injection kinetics and also functioning as a blocking layer to cover the TiO2 core from the outer QDs and redox couple, thereby reducing the recombination of electrons from the TiO2 with the electrolyte or with the QDs. Electrochemical impedance measurements has been measured and discussed in detail providing a detailed analysis of charge transport processes in QDSSCs.
AB - Charge recombination is considered as one of the most significant factors in hindering the photovoltaic performance of quantum dot-sensitized solar cells (QDSSCs). In addition, expand the light absorption range to the near-infrared region in QDSSCs increasing the generated photocurrent. A significant enhancement in the power conversion efficiency (PCE) of QDSSCs has been obtained by charge recombination control and enhanced light harvesting. In this respect, PbCdS layer is introduced between TiO2 and CdS QDs via a facile successive ionic layer absorption and reaction (SILAR) method in order to further improve the cell performance. For the first time a photoanode assembly composed of TiO2/PbCdS/CdS was prepared in QDSSCs. The photovoltaic parameters were significantly enhanced with the incorporation of a PbCdS intermediate layer between TiO2 and CdS QDs but varied appreciably with the SILAR cycles of PbCdS. When four SILAR cycle layer was applied, the PCE is as high as 3.35%, which is higher than the efficiency of 1.84% for the solar cell without PbCdS layer. The improved performance of the TiO2/PbCdS/CdS-based QDSSCs was attributed to the PbCdS layer can enhance the light harvesting to release more excitons. In addition, the PbCdS layer accelerates the electron injection kinetics and also functioning as a blocking layer to cover the TiO2 core from the outer QDs and redox couple, thereby reducing the recombination of electrons from the TiO2 with the electrolyte or with the QDs. Electrochemical impedance measurements has been measured and discussed in detail providing a detailed analysis of charge transport processes in QDSSCs.
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U2 - 10.1016/j.jelechem.2017.02.005
DO - 10.1016/j.jelechem.2017.02.005
M3 - Article
AN - SCOPUS:85012215381
SN - 0368-1874
VL - 788
SP - 131
EP - 136
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
ER -