Cited 7 time in
Cited 7 time in
Enhanced power conversion efficiency of dye-sensitized solar cells with Li2SiO3-modified photoelectrode
- Enhanced power conversion efficiency of dye-sensitized solar cells with Li2SiO3-modified photoelectrode
- Kim, JT[Kim, Jong Tae]; Lee, SH[Lee, Sung Ho]; Han, YS[Han, Yoon Soo]
- DGIST Authors
- Kim, JT[Kim, Jong Tae]
- Issue Date
- Applied Surface Science, 333, 134-140
- Article Type
- Conduction Band Edge; Conduction Band Edge Shift; Conduction Bands; Conversion Efficiency; Current Voltage Characteristics; Dye-Sensitized Solar Cell; Dye-Sensitized Solar Cells (DSCs); Electrochemical Impedance Spectra; Electrodes; Lithium; Lithium Silicate; Lithium Silicates; Open Circuit Voltage; Photo-Electrodes; Power Conversion Efficiencies; Reference Devices; Silicates; Soaking Process; Solar Cells; Surface Dipole; Surface Modifiers
- The effects of lithium silicate (LS) as a surface modifier on the performance of dye-sensitized solar cells (DSSCs) were studied. LS-modified TiO2 electrodes (LS-TiO2/FTO) prepared by a soaking process were applied to the photoelectrodes of DSSCs. The reference device without any modification showed performance of 0.68 V of open-circuit voltage (Voc), 21.40 mA/cm2 of short-circuit current (Jsc), and 63.21% of fill factor (FF), which led to a power conversion efficiency (PCE) of 9.20%, whereas for the device with the LS-TiO2/FTO electrode, the PCE was increased to 10.58% (Voc = 0.79 V, Jsc = 20.22 mA/cm2, and FF = 66.21%). By monitoring the changes in dark current-voltage characteristics, normalized IPCE spectra, and electrochemical impedance spectra, it was revealed that the LS modification induced the formation of a surface dipole on the TiO2 photoelectrode, leading to the conduction band edge shift of TiO2 toward a negative direction, and thus to an enhancement in Voc and a decrease in Jsc. © 2015 Elsevier B.V. All rights reserved.
- Elsevier B.V.
There are no files associated with this item.
- Division of Nano∙Energy Convergence Research1. Journal Articles
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.