TY - JOUR
T1 - Solid-state processing of organic semiconductors
AU - Baklar, Mohammed A.
AU - Koch, Felix
AU - Kumar, Avinesh
AU - Domingo, Ester Buchaca
AU - Campoy-Quiles, Mariano
AU - Feldman, Kirill
AU - Yu, Liyang
AU - Wobkenberg, Paul
AU - Ball, James
AU - Wilson, Rory M.
AU - McCulloch, Iain
AU - Kreouzis, Theo
AU - Heeney, Martin
AU - Anthopoulos, Thomas
AU - Smith, Paul
AU - Stingelin, Natalie
N1 - Generated from Scopus record by KAUST IRTS on 2023-02-14
PY - 2010/9/15
Y1 - 2010/9/15
N2 - Solid-state processing of conjugated small molecular, oligomeric and polymeric compounds was conducted. Solid, powdered material was placed in a hot press, followed by compression molding well below the melting temperatures of the species, typically at pressures of approximately 10 30 kN cm-2. In order to investigate whether or not solid-state processing deteriorated electronic properties of the semiconductors, time-of-flight (TOF) photoconductivity experiments were conducted, which allow determination of bulk charge transport across thin film architectures. A typical small-molecular compound (6T) and two polymeric species P3HT and the liquid-crystalline PBTTT-C16, were selected. It was demonstrated that bulk carrier mobilities derived from TOF studies did not deteriorate, but in some cases actually could be significantly enhanced when compared to conventionally processed structures. Interfacial charge transport both for electrons and holes was not affected, despite processing the organic semiconductors in light and air.
AB - Solid-state processing of conjugated small molecular, oligomeric and polymeric compounds was conducted. Solid, powdered material was placed in a hot press, followed by compression molding well below the melting temperatures of the species, typically at pressures of approximately 10 30 kN cm-2. In order to investigate whether or not solid-state processing deteriorated electronic properties of the semiconductors, time-of-flight (TOF) photoconductivity experiments were conducted, which allow determination of bulk charge transport across thin film architectures. A typical small-molecular compound (6T) and two polymeric species P3HT and the liquid-crystalline PBTTT-C16, were selected. It was demonstrated that bulk carrier mobilities derived from TOF studies did not deteriorate, but in some cases actually could be significantly enhanced when compared to conventionally processed structures. Interfacial charge transport both for electrons and holes was not affected, despite processing the organic semiconductors in light and air.
UR - https://onlinelibrary.wiley.com/doi/10.1002/adma.200904448
UR - http://www.scopus.com/inward/record.url?scp=77957321520&partnerID=8YFLogxK
U2 - 10.1002/adma.200904448
DO - 10.1002/adma.200904448
M3 - Article
C2 - 20845373
SN - 0935-9648
VL - 22
SP - 3942
EP - 3947
JO - Advanced Materials
JF - Advanced Materials
IS - 35
ER -