文摘
The performance enhancement of dye-sensitized solar cells (DSCs) in lithium-free and lithium-containingelectrolytes under visible light-soaking was examined by impedance spectroscopy and photovoltage transientdecay measurements. The improvement was found to arise from the formation of electronic transport levelsclose to the conduction band, resulting most likely from photoinduced proton intercalation in the TiO2nanoparticles. These shallow trapping states accelerate the charge carrier transport within the nanocrystallinefilms without deteriorating the open circuit photovoltage. Subjecting the cells to forward bias in the darkproduces a similar effect, whereas the introduction of lithium ions in the electrolyte suppresses the phenomenadue to prevailing lithium ion intercalation. The redistribution of localized states in the band gap of TiO2 andthe resulting conduction band edge movement appears to play a significant role in the performance of theDSC.