TY - JOUR
T1 - The hole in the bucky
T2 - Structure-property mapping of closed-: Vs. open-cage fullerene solar-cell blends via temperature/composition phase diagrams
AU - Matrone, Giovanni Maria
AU - Gutiérrez-Meza, Elizabeth
AU - Balzer, Alex H.
AU - Khirbat, Aditi
AU - Levitsky, Artem
AU - Sieval, Alexander B.
AU - Frey, Gitti L.
AU - Richter, Lee J.
AU - Silva, Carlos
AU - Stingelin, Natalie
N1 - Publisher Copyright: © 2021 The Royal Society of Chemistry.
PY - 2021/12/7
Y1 - 2021/12/7
N2 - The morphology development of polymer-based blends, such as those used in organic photovoltaic (OPV) systems, typically arrests in a state away from equilibrium-how far from equilibrium this is will depend on the materials chemistry and the selected assembly parameters/environment. As a consequence, small changes during the blend assembly alter the solid-structure development from solution and, in turn, the final device performance. Comparing an open-cage ketolactam fullerene with the prototypical[6,6]-phenyl-C61-butyric acid methyl ester in blends with poly[2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT), we demonstrate that experimentally established, non-equilibrium temperature/composition phase diagrams can be useful beyond rationalization of optimum blend composition for OPV device performance. Indeed, they can be exploited as tools for rapid, qualitative structure-property mapping, providing insights into why apparent similar donor:acceptor blends display different optoelectronic processes resulting from changes in the phase-morphology formation induced by the different chemistries of the fullerenes.
AB - The morphology development of polymer-based blends, such as those used in organic photovoltaic (OPV) systems, typically arrests in a state away from equilibrium-how far from equilibrium this is will depend on the materials chemistry and the selected assembly parameters/environment. As a consequence, small changes during the blend assembly alter the solid-structure development from solution and, in turn, the final device performance. Comparing an open-cage ketolactam fullerene with the prototypical[6,6]-phenyl-C61-butyric acid methyl ester in blends with poly[2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT), we demonstrate that experimentally established, non-equilibrium temperature/composition phase diagrams can be useful beyond rationalization of optimum blend composition for OPV device performance. Indeed, they can be exploited as tools for rapid, qualitative structure-property mapping, providing insights into why apparent similar donor:acceptor blends display different optoelectronic processes resulting from changes in the phase-morphology formation induced by the different chemistries of the fullerenes.
UR - http://www.scopus.com/inward/record.url?scp=85120405866&partnerID=8YFLogxK
U2 - 10.1039/d1tc03082e
DO - 10.1039/d1tc03082e
M3 - مقالة
SN - 2050-7534
VL - 9
SP - 16304
EP - 16312
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 45
ER -