In this work, we studied the performance enhancement of organic thin-film solar cells (OSCs) originating from the presence of diffraction gratings on the surface of the active layer. Two types of diffraction gratings, periodic gratings (Blu-ray disc recordable: BD-R) and quasi-random gratings (Blu-ray disc: BD), were employed as master templates for grating structures. The grating structures were introduced to the surfaces of poly(3-hexylthiophene) (P3HT):phenyl-C-butyric acid methyl ester (PCBM) films, which were the active layers of the solar cells. The addition of the grating structures led to an increase of light absorption in the absorption region of P3HT:PCBM induced by light scattering. Furthermore, the grating-coupled surface plasmon resonance generated additional light absorption peaks. With illumination of non-polarized light at a normal incident angle, the short-circuit current densities of the BD-R and BD solar cells improved by 11.05% and 10.6%, respectively. Efficiency improvements of 19.28% and 3.21% were also observed for the BD-R and BD devices, respectively. Finally, the finite-difference time-domain simulation results revealed an enhanced electric field in the P3HT:PCBM layer, especially in the BD-R OSC devices.
Gold quantum dots (AuQDs) are employed as photosensitizers in organic thin‐film solar cells (OSCs) to improve their photoelectric conversion properties. Three types of AuQDs with different fluorescence emission wavelengths are used: blue (B‐AuQDs), green (G‐AuQDs), and red (R‐AuQDs). AuQDs are loaded into the poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) thin‐film layer of OSCs. UV–vis spectra, atomic force microscope images, current density–voltage characteristics, and impedance spectra of the fabricated devices are measured for the three aforementioned types of AuQDs. All types of AuQDs improve the photoelectric conversion properties, and the G‐AuQD‐loaded OSCs exhibit the best improvement, exhibiting an efficiency increase of 10% compared with OSCs without the AuQDs. The fluorescence/photosensitization of the AuQDs plays an important role in the enhancement of the OSCs. Finite‐difference time‐domain simulations indicate increased electric field intensity due to a small degree of AuQDs aggregation.
PSS) thin-film layer of organic thin-film solar cells (OSCs). UV-vis spectra, atomic force microscopy (AFM) images, current density versus voltage properties, and the impedance spectra of the fabricated devices were recorded at various concentrations of UL-AuNPs. We found that the efficiency of the OSCs with UL-AuNPs was not only higher than that of a reference cell without nanoparticles but also higher than that of OSCs with spherical AuNPs. Finite-difference time-domain (FDTD) simulation indicated that the electric field around the UL-AuNPs increased due to the presence of nanothorns.
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