Year: 2013
Type: article
Abstract: A combination of transient photovoltage (TPV), voltage dependent charge extraction (CE), and time delayed collection field (TDCF) measurements is applied to poly[[4,8‐bis[(2‐ethylhexyl)oxy]benzo[1,2‐b:4,5‐b']dithiophene‐2,6‐diyl] [3‐fluoro‐2‐[(2‐ethylhexyl)carbonyl] thieno[3,4‐b]thiophenediyl]] (PTB7):[6,6]‐phenyl‐C71‐butyric acid (PC 71 BM) bulk heterojunction solar cells to analyze the limitations of photovoltaic performance. Devices are processed from pure chlorobenzene (CB) solution and a subset is optimized with 1,8‐diiodooctane (DIO) as co‐solvent. The dramatic changes in device performance are discussed with respect to the dominating loss processes. While in the devices processed from CB solution severe geminate and nongeminate recombination is observed, the use of DIO facilitates efficient polaron pair dissociation and minimizes geminate recombination. Thus, from the determined charge carrier decay rate under open circuit conditions and the voltage dependent charge carrier densities n ( V ), the nongeminate loss current J loss of the samples with DIO alone enables the reconstruction of the current/voltage ( j / V ) characteristics across the whole operational voltage range. Geminate and nongeminate losses are considered to describe the j / V response of cells prepared without additive, but lead to a clearly overestimated device performance. The deviation between measured and reconstructed j / V characteristics is attributed to trapped charges in isolated domains of pure fullerene phases.
Source: Advanced Functional Materials
Authors: Alexander Foertig, Juliane Kniepert, Markus Gluecker, Thomas Brenner, Vladimir Dyakonov, Dieter Neher, Carsten Deibel
Language: English
Subfield: Electrical and Electronic Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: green
Award: G1941170345
OpenAlex ID: W2021876790