The Journal of Physical Chemistry C · 2014 · 30 citations · 47 references
EngineeringMaterials EngineeringMaterials ScienceOptoelectronicsSemiconductor DevicesSemiconductor MaterialsPhotovoltaic DevicesQuantum DotsSemiconductor Device MaterialsSemiconductor InterfacesSemiconductor Thin FilmsSolar CellsElectron Transport LayersEnergy Conversion EfficiencyFill FactorPower ConversionPower Conversion EfficiencyQuantum Dot Solar CellsSemiconductor Quantum DotsThin Oxide Films
ZnO thin films fabricated by a low-temperature sol–gel conversion method (L-ZnO) were employed as n-type electron-transporting layers (ETLs) in depleted-heterojunction quantum dot solar cells (DH-QDSCs). Thin films of PbS (∼200 nm) fabricated by spin-coating a colloidal PbS QD solution layer by layer were used as the p-type photoactive layers. The L-ZnO films functioned as efficient n-type ETLs by fully completely depleting the PbS active layers, and they displayed performances much higher than those of conventional ZnO nanoparticle-based ETLs. The morphologies and chemical compositions of the L-ZnO ETLs varied with the annealing conditions. These factors, in turn, had a marked effect on the charge-transfer characteristics at the L-ZnO/PbS interfaces of the DH-QDSCs. The power conversion efficiency (PCE) of the DH-QDSCs using the optimized L-ZnO films as ETLs was 3.93%, with the fill factor (FF) being 0.60, whereas the PCE of the cells using the ZnO nanoparticle-based films was 1.62%, with the FF being 0.53. Thus, the sol–gel-derived L-ZnO films, which could be fabricated using a simple, low-temperature, solution-based process, exhibited desirable performance as ETLs in DH-QDSCs.
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