Title of article :
The role of the double peaked absorption spectrum in the efficiency of solar cells based on donor–acceptor–donor copolymers
Author/Authors :
Canestraro، نويسنده , , Carla D. and Rodrigues، نويسنده , , Paula C. and Marchiori، نويسنده , , Cleber F.N. and Schneider، نويسنده , , Camila B. and Akcelrud، نويسنده , , Leni and Koehler، نويسنده , , Marlus and Roman، نويسنده , , Lucimara S. Roman، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
8
From page :
2287
To page :
2294
Abstract :
An interesting procedure to optimize organic solar cells is to lower the band gap of the polymer layer by introducing alternating donor–acceptor (D–A) units in the backbone. However, many aspects of the fundamental physics involved in this low band gap design and their relation with the solar cell performance are still unknown. In this work we address those aspects by studying electro-optical properties of the poly(9,9′-dioctyl-2,7-fluorenediylvinylene-co-2,5-thiophene) (PFTBT) copolymer, which consists of a fluorene linked by a vinylene to a donor–acceptor–donor segment (benzothiadiazole unit between 2 thiophenes groups). Using density functional theory we have performed a detailed analysis of the geometric structure, ground state electronic structure and excited state vertical transitions of the PFTBT. By comparing the results of this theoretical analysis with the solution and thin film UV–vis absorption spectra we were able to identify the main chemical units involved in the two strong transitions responsible for the PFTBT dual absorption. We have found that the absence of alkyl substitutions on the thiophene units increases the planarity of the polymer backbone leading to a thin film with a higher absorption at low wavelengths and larger hole mobility compared to an analogous copolymer. Improved photovoltaic properties of PFTBT were demonstrated by fabricating bilayer devices using C60 as acceptor. The power conversion efficiency reached 1% which is comparable to those obtained using optimized alternating copolymers in the bulk heterojunction architecture. Finally we found that the light absorption around the “blue” band has a higher efficiency on photocarrier generation because it involves the transition from a delocalized occupied state to a more localized excited state in the polymer backbone. This lower initial electron–hole spatial overlap facilitates the exciton dissociation which increases the photocurrent yield.
Keywords :
Dual absorption , Bilayer organic solar cells , Density functional theory , Donor–acceptor–donor polymer
Journal title :
Solar Energy Materials and Solar Cells
Serial Year :
2011
Journal title :
Solar Energy Materials and Solar Cells
Record number :
1486037
Link To Document :
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