Solvent dependent ordering of poly(3-dodecylthiophene) in thin films

Abstract

The strong influence of solvents on the ordering of poly(3-dodecylthiophene) (P3DDT) due to edge-on oriented stacking, in the spin-coated thin film on the Si substrate, both near the substrate and away from it, depending upon the substrate surface nature, is observed from the X-ray reflectivity study. The absence of any appreciable amount of coil-like P3DDT chains (i.e. charge localized states) and formation of π-stacked aggregates (i.e. charge delocalized states) in the spin-coated thin films, with slightly better uniformity for the film prepared from toluene (TL) compared to that prepared from chloroform (CF) and chlorobenzene (CB), are well evident from the optical absorption study. No ordering near the weakly hydrophobic H-Si substrate is found in the films prepared from TL, probably due to less diffusion of P3DDT in TL and the appreciable pinning (film-substrate interaction) effect, while appreciable ordering near the film-air interface, overcoming the pinning effect, is likely to be related to the moderate values of the viscosity and the evaporation rate of the solvent. A better ordered Form-I-like relaxed structure near the film-substrate interface and a less ordered interpenetrating Form-II-like structure toward the film-air interface are found in the films prepared from CF, probably related to the low viscosity and high evaporation rate, respectively, of the solvent. Less ordered and mixed but more toward Form-II-like structures are formed throughout the film prepared from CB, probably due to the high viscosity of the solvent, even though its evaporation rate is low. The high evaporation rate of CF and high viscosity of CB probably create hindrance in the formation of continuous films on the weakly hydrophilic O-Si substrate at low speed, while the moderate values of both the parameters for TL, help to form continuous films on the O-Si substrate even at low speed. Such moderate values also help to form less variable (and more toward Form-I-like) structures and better ordering in the latter film. The relative fluctuation between aggregates along the film-thickness is, however, found slightly more in the film prepared from TL compared to that prepared from CF.

Vertically Oriented Nanostructures of Poly(3-dodecylthiophene)-Containing Rod–Coil Block Copolymers

“…The morphology of as-cast STAR-SDDT thin film before thermal annealing corresponds to kinetical trapped one during spin-coating rather than thermal equilibrium. Therefore, the morphology depends on different swelling ratios between PS and P3DDT blocks to each solvent as well as different boiling points of a solvent. ,, However, unlike the as-cast film, after thermal annealing, the same morphology was observed (Figure b,d,f). This is because thermal annealing was performed at 200 °C, which is higher than the glass transition temperature of PS (∼105 °C) and melting temperature ( T m ) of P3DDT (∼140 °C) as well as the boiling point of each solvent.…”

pH-dependent size and structural transition in P123 micelle induced gold nanoparticles

“…36,37 For comparison UV-vis absorption spectra of the mixed solutions of P123 + water were also carried out. 36,37 For comparison UV-vis absorption spectra of the mixed solutions of P123 + water were also carried out.…”

“…Time dependent UV-vis absorption spectra of the mixed solutions of HAuCl 4 + P123 + water were carried out with a UV-vis spectrophotometer (Lambda 750, PerkinElmer). 36,37 For comparison UV-vis absorption spectra of the mixed solutions of P123 + water were also obtained. The instrument was operated in spectrum mode with a wavelength interval of 1 nm and the samples were held in quartz cuvettes with a path length of 1 cm.…”

“…For that, the evolution and final state of mixed aqueous solution, containing TBP and gold salt, of different pHvalue, were monitored using ultraviolet-visible (UV-vis) spectroscopy [28][29][30][31][32][33][34][35][36][37] and dynamic light scattering (DLS) [37][38][39] techniques, respectively, while the morphology of the AuNPs and aggregates in the final states were imaged through transmission electron microscopy (TEM). For that, the evolution and final state of mixed aqueous solution, containing TBP and gold salt, of different pHvalue, were monitored using ultraviolet-visible (UV-vis) spectroscopy [28][29][30][31][32][33][34][35][36][37] and dynamic light scattering (DLS) [37][38][39] techniques, respectively, while the morphology of the AuNPs and aggregates in the final states were imaged through transmission electron microscopy (TEM).…”

“…In this paper, we have tried to understand the role of the pH value of the TBP micellar solution on the simultaneous reduction of gold ions and the formation of AuNPs using complementary techniques. For this, the evolution and nal state of the mixed aqueous solution, containing TBP and the gold salt, of different pH values, were monitored using ultraviolet-visible (UV-vis) spectroscopy [28][29][30][31][32][33][34][35][36][37] and dynamic light scattering (DLS) [37][38][39] techniques, respectively, while the morphology of the AuNPs and aggregates in the nal states were imaged through transmission electron microscopy (TEM). 40 The presence of isolated large AuNPs and large micelles loaded with small AuNPs is clearly evident.…”