Controlling additive behavior to reveal an alternative morphology formation mechanism in polymer : fullerene bulk-heterojunctions. Issue 41 (3rd October 2016)
- Record Type:
- Journal Article
- Title:
- Controlling additive behavior to reveal an alternative morphology formation mechanism in polymer : fullerene bulk-heterojunctions. Issue 41 (3rd October 2016)
- Main Title:
- Controlling additive behavior to reveal an alternative morphology formation mechanism in polymer : fullerene bulk-heterojunctions
- Authors:
- Güldal, Nusret S.
Berlinghof, Marvin
Kassar, Thaer
Du, Xiaoyan
Jiao, Xuechen
Meyer, Markus
Ameri, Tayebeh
Osvet, Andres
Li, Ning
Destri, Giovanni Li
Fink, Rainer H.
Ade, Harald
Unruh, Tobias
Brabec, Christoph J. - Abstract:
- Abstract : The high solubility of DPP-TT-T in 1, 8-diiodooctane leads the microstructure formation towards thermodynamic equilibrium. Abstract : One of the most employed morphology optimization methods to design better performing organic photovoltaic devices is ink formulation engineering with additives. In this work, by employing a suboptimal host solvent mixture and 1, 8-diiodooctane (DIO) as a very optimal solvent for both components in poly-thieno[3, 2 b ]thiophene-diketopyrrolopyrrole- co -thiophene (DPP-TT-T)-based bulk-heterojunctions (BHJ), an alternative, previously unknown mechanism of additive behavior on BHJ microstructure formation is presented. In situ characterization methods involving grazing incidence X-ray diffraction, white-light reflectometry, laser light scattering and photoluminescence during film drying reveal that the microstructure formation under the influence of DIO is led towards thermodynamic equilibrium during host solvent drying, and the kinetics of morphology formation ( i.e. polymer crystallization, fullerene aggregation…) are controlled dominantly by the additive during its evaporation. Ex situ X-ray-based characterization methods, such as scanning transmission X-ray microspectroscopy (STXM) and resonant soft X-ray scattering (R-SoXS), additionally reveal that the microstructure of dried films favors smaller domain sizes with purer domains, smaller fullerene aggregates, bimodal polymer crystallization relative to the substrate and moreAbstract : The high solubility of DPP-TT-T in 1, 8-diiodooctane leads the microstructure formation towards thermodynamic equilibrium. Abstract : One of the most employed morphology optimization methods to design better performing organic photovoltaic devices is ink formulation engineering with additives. In this work, by employing a suboptimal host solvent mixture and 1, 8-diiodooctane (DIO) as a very optimal solvent for both components in poly-thieno[3, 2 b ]thiophene-diketopyrrolopyrrole- co -thiophene (DPP-TT-T)-based bulk-heterojunctions (BHJ), an alternative, previously unknown mechanism of additive behavior on BHJ microstructure formation is presented. In situ characterization methods involving grazing incidence X-ray diffraction, white-light reflectometry, laser light scattering and photoluminescence during film drying reveal that the microstructure formation under the influence of DIO is led towards thermodynamic equilibrium during host solvent drying, and the kinetics of morphology formation ( i.e. polymer crystallization, fullerene aggregation…) are controlled dominantly by the additive during its evaporation. Ex situ X-ray-based characterization methods, such as scanning transmission X-ray microspectroscopy (STXM) and resonant soft X-ray scattering (R-SoXS), additionally reveal that the microstructure of dried films favors smaller domain sizes with purer domains, smaller fullerene aggregates, bimodal polymer crystallization relative to the substrate and more face-on molecular orientation relative to the donor/acceptor interface, which at the end lead to better performing devices with power conversion efficiencies ranging from 1.25% to 4.68%. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 41(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 41(2016)
- Issue Display:
- Volume 4, Issue 41 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 41
- Issue Sort Value:
- 2016-0004-0041-0000
- Page Start:
- 16136
- Page End:
- 16147
- Publication Date:
- 2016-10-03
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6ta07023j ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1289.xml