Diketopyrrolopyrrole-based polymer:fullerene nanoparticle films with thermally stable morphology for organic photovoltaic applications
Autor: | Holmes, NP, Vaughan, B, Williams, EL, Kroon, R, Anderrson, MR, Kilcoyne, ALD, Sonar, P, Zhou, X, Dastoor, PC, Belcher, WJ |
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Rok vydání: | 2017 |
Předmět: | |
Zdroj: | MRS Communications, vol 7, iss 1 Holmes, NP; Vaughan, B; Williams, EL; Kroon, R; Anderrson, MR; Kilcoyne, ALD; et al.(2017). Diketopyrrolopyrrole-based polymer:fullerene nanoparticle films with thermally stable morphology for organic photovoltaic applications. MRS Communications, 7(1), 67-73. doi: 10.1557/mrc.2017.3. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/3b56t2mz |
DOI: | 10.1557/mrc.2017.3. |
Popis: | © Materials Research Society 2017. Polymer:fullerene nanoparticles (NPs) offer two key advantages over bulk heterojunction (BHJ) films for organic photovoltaics (OPVs), water-processability and potentially superior morphological control. Once an optimal active layer morphology is reached, maintaining this morphology at OPV operating temperatures is key to the lifetime of a device. Here we study the morphology of the PDPP-TNT (poly{3,6-dithiophene-2-yl-2,5-di(2-octyldodecyl)-pyrrolo[3,4-c]pyrrole-1,4-dione-alt-naphthalene}):PC71BM ([6,6]-phenyl C71 butyric acid methyl ester) NP system and then compare the thermal stability of NP and BHJ films to the common poly(3-hexylthiophene) (P3HT): phenyl C61 butyric acid methyl ester (PC61BM) system. We find that material T g plays a key role in the superior thermal stability of the PDPP-TNT:PC71BM system; whereas for the P3HT:PC61BM system, domain structure is critical. |
Databáze: | OpenAIRE |
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