of polymers was performed using a PerkinElmer Spectrum GX-A FTIR spectrophotometer.
The analysis was carried out in the wavenumber range of 4000–400
cm–1 with a resolution of 4 cm–1. 1H NMR spectroscopy of polymers was carried out using
a Bruker AVANCE spectrometer with CDCl3 as solvent at a
frequency of 300 MHz. TGA was carried out on a TA instrument, model
SDT-2960. The temperature range of the analysis was 30–900
°C in a nitrogen atmosphere at a heating rate of 10 °C per
minute. DSC studies were conducted on a TA instrument model 2920 modulated
differential scanning calorimeter at a heating rate of 10 °C/min
under a N2 atmosphere. The surface morphology of materials
was traced by FESEM on a Hitachi SU6600 variable pressure field-emission
scanning electron microscope instrument. AFM analysis was carried
out on an AFM instrument (Agilent Technologies 5500). The static CAs
of the P-UT films were measured with a Data Physics contact angle
instrument OCA85 15EC (Drop size-5 μL, curve-fitting method).
The transparency of P-UTs was measured by solid-state UV–vis
spectroscopy using a PerkinElmer LAMDA 950 instrument.