Chemistry of Materials · 2019 · 27 citations · 52 references
Natural SciencesChemistryMaterials ScienceMaterials ChemistryPolymer ChemistryPolymer MaterialsOrganic Electronic MaterialsOrganic SemiconductorsPhotovoltaic DevicesPhotovoltaic MaterialsSolar Cell MaterialsSolar CellsEnergy Conversion EfficiencyHole TransportInterchain InteractionsOrganic Photovoltaic CellsOrganic PhotovoltaicsOrganic Solar CellsPower ConversionPower Conversion Efficiency
Polymer solar cells (PSCs) processed from non-halogenated solvents are favorable for large scale production. However, the photovoltaic performance of devices from non-halogenated solvents is generally inferior to that of the counterparts from halogenated solvents. Herein, we report the utilization of 5-alkyl-4-(methylthio)thiophene (MTT) as a conjugated side chain of the polymeric donor to achieve efficient PSCs processed from toluene. The derived polymer PMTT56 exhibits lower energy levels than the 5-alkyl-4-methoxythiophene (MOT) counterpart (PMOT39) and 5-(alkylthio)thiophene counterpart (PEHTT). PMTT56 is superior to PMOT39 with an enhanced interchain interaction and hole mobility, and also shows better solubility than PEHTT in toluene. In toluene-processed PSCs, the PMTT56 devices deliver a power conversion efficiency (PCE) of up to 12.6% with IT-2F as the acceptor. By introducing [6,6]-phenyl C71-butyric acid methyl ester (PC71BM) as the second acceptor, a remarkable PCE of 13.2% is further achieved in the ternary devices, which is among the best for PSCs processed from toluene. Our study presents a fine-tuning approach to develop efficient organic photovoltaic materials processed from non-halogenated solvents.
52
VMD: Visual molecular dynamics
William Humphrey, Andrew Dalke, Klaus Schulten · Journal of Molecular Graphics · 1996 · 66.6K citations
Multiwfn: A multifunctional wavefunction analyzer
Tian Lu, Feiwu Chen · Journal of Computational Chemistry · 2011 · 43K citations