Table 2. Optical and Energetic Properties of the Neutral Polymers.
| polymer | λmax (nm) |
cEoptg (eV) | dDR [rubbing temperature] (°C)] | eE(ox)onset vs Fc/Fc+ (V) | fΦwf (eV) | |
|---|---|---|---|---|---|---|
| solutiona | thin filmb | |||||
| P3HT | 455 | 561 | 1.91 | 16 [220] | 0.05 | 4.65 |
| Tref | 456 | 560 | 1.91 | 10 [180] | 0.06 | 4.67 |
| T19 | 469 | 550 | 1.94 | 6 [150] | 0.03 | 4.71 |
| T24 | 471 | 549 | 1.95 | 3 [80] | 0.03 | 4.70 |
Measured by UV–vis absorbance spectroscopy from 0.01 mg mL–1 polymer solutions in chlorobenzene set at 30 °C using a Peltier cooler.
Measured by UV–vis absorbance spectroscopy from thin films spun from 10 mg mL–1 ODCB solutions at 80 °C at 2000 rpm for 90 s onto glass slides.
Estimated from the optical onset of absorbance. Energy (eV) = 1240 (eV nm)/λ (nm).
Dichroic ratio was calculated using DR = A∥/A⊥.
Measured by cyclic voltammetry from the onset of oxidation of polymer thin films drop-cast onto a glassy carbon electrode from 1 mg mL–1 chloroform solutions in acetonitrile with 0.1 M tetrabutylammonium hexafluorophosphate as the supporting electrolyte. A platinum wire, carbon electrode, and Ag/Ag+ electrode were used as the counter, working, and reference electrodes, respectively. Fc/Fc+ = Ag/Ag+ – 0.115 V.
Work function measured using PESA on two polymer thin films doctor-bladed onto ITO-coated glass from 10 mg mL–1 solutions in chlorobenzene.