Autor segons l'article: Granero, P. Balderrama, V.S. Ferré-Borrull, J. Pallarès, J. Marsal, L.F.
Departament: Enginyeria Electrònica, Elèctrica i Automàtica
e-ISSN: 1089-7550
Resum: By means of ?nite-element numerical modeling, we analyze the in?uence of the nanostructured dissociation interface geometry on the behavior of interdigitated heterojunction full organic solar cells. A systematic analysis of light absorption, exciton diffusion, and carrier transport, all in the same numerical framework, is carried out to obtain their dependence on the interface geometrical parameters: pillar diameter and height, and nanostructure period. Cells are constituted of poly(3-hexylthiophene) (P3HT) and 1-(3-methoxycarbonyl)-propyl-1-phenyl-(6,6)C61. Results show that light absorption is maximum for pillar heights of 80 nm and 230 nm. However, due to the short exciton diffusion length of organic materials, the analysis of the exciton diffusion process reveals that the 80 nm thickness gives rise to a higher photocurrent, except for the smaller pillar diameters. In terms of ef?ciency, it has been observed that the charge carrier transport is weakly dependent on the geometric parameters of the nanostructured interface if compared with the exciton diffusion process. The optimal cell is a device with a pillar height of 80 nm, a structure period of 25 nm, and a ratio of the nanopillar diameter to the period of 0.75, with an ef?ciency 3.6 times higher than the best planar bilayer reference device. This structure is such that it reaches a compromise between having a high proportion of P3HT to increase light absorption but preserving a small pillar diameter and interpillar distance to ensure an extended exciton dissociation interface.
Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
Paraula clau altres idiomes: Excitons Finite element analysis Light absorption organic compounds Photoconductivity
ISSN: 0021-8979
Pàgina final: 7
Volum de revista: 113
Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
Entitat: Universitat Rovira i Virgili.
Any de publicació de la revista: 2013
Pàgina inicial: 1