TY - JOUR
T1 - A New Tetracyclic Lactam Building Block for Thick, Broad-Bandgap Photovoltaics
AU - Kroon, Renee
AU - Mendaza, Amaia
AU - Himmelberger, Scott
AU - Bergqvist, Jonas
AU - Backe, Olof
AU - Faria, Gregoria
AU - Gao, Feng
AU - Obaid, Abdulmalik
AU - Zhuang, Wenliu
AU - Gedefaw, Desta
AU - Olsson, Eva
AU - Inganas, Olle
AU - Salleo, Alberto
AU - Muller, Christian
AU - Andersson, Mats R.
PY - 2014/8/20
Y1 - 2014/8/20
N2 - A new tetracyclic lactam building block for polymer semiconductors is reported that was designed to combine the many favorable properties that larger fused and/or amide-containing building blocks can induce, including improved solid-state packing, high charge carrier mobility, and improved charge separation. Copolymerization with thiophene resulted in a semicrystalline conjugated polymer, PTNT, with a broad bandgap of 2.2 eV. Grazing incidence wide-angle X-ray scattering of PTNT thin films revealed a strong tendency for face-on π-stacking of the polymer backbone, which was retained in PTNT:fullerene blends. Corresponding solar cells featured a high open-circuit voltage of 0.9 V, a fill factor around 0.6, and a power conversion efficiency as high as 5% for >200 nm thick active layers, regardless of variations in blend stoichiometry and nanostructure. Moreover, efficiencies of >4% could be retained when thick active layers of ∼400 nm were employed. Overall, these values are the highest reported for a conjugated polymer with such a broad bandgap and are unprecedented in materials for tandem and particularly ternary blend photovoltaics. Hence, the newly developed tetracyclic lactam unit has significant potential as a conjugated building block in future organic electronic materials.
AB - A new tetracyclic lactam building block for polymer semiconductors is reported that was designed to combine the many favorable properties that larger fused and/or amide-containing building blocks can induce, including improved solid-state packing, high charge carrier mobility, and improved charge separation. Copolymerization with thiophene resulted in a semicrystalline conjugated polymer, PTNT, with a broad bandgap of 2.2 eV. Grazing incidence wide-angle X-ray scattering of PTNT thin films revealed a strong tendency for face-on π-stacking of the polymer backbone, which was retained in PTNT:fullerene blends. Corresponding solar cells featured a high open-circuit voltage of 0.9 V, a fill factor around 0.6, and a power conversion efficiency as high as 5% for >200 nm thick active layers, regardless of variations in blend stoichiometry and nanostructure. Moreover, efficiencies of >4% could be retained when thick active layers of ∼400 nm were employed. Overall, these values are the highest reported for a conjugated polymer with such a broad bandgap and are unprecedented in materials for tandem and particularly ternary blend photovoltaics. Hence, the newly developed tetracyclic lactam unit has significant potential as a conjugated building block in future organic electronic materials.
UR - http://www.scopus.com/inward/record.url?scp=84906336056&partnerID=8YFLogxK
U2 - 10.1021/ja5051692
DO - 10.1021/ja5051692
M3 - Article
SN - 0002-7863
VL - 136
SP - 11578
EP - 11581
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 33
ER -