A series of low bandgap polymers containing thiophene and diketopyrrolopyrrole (DPP) units were synthesized and their electrochromic (EC) properties were investigated. It was found that the ratio (Rda) of thiophene to DPP units correlates to the EC properties, in particular optical contrast (ΔT) and coloration efficiency (CE) in the visible and near-infrared spectral regions (e.g., 1310 nm). At the wavelength of 1310 nm, the CE of polymer P2 (Rda = 3 : 1) and ΔT of polymer P4 (Rda = 4 : 1) reached the high values of 1383 cm2 C-1 and 81.5%, respectively. Polymer P3 (Rda = 3.5 : 1) had a relatively short switching time of 1.24 s from the doped state to neutral state. Colors of polymer films changed reversibly between green or blue (neutral st...
Three dithienylpyrroles (1-(4-(methylthio)phenyl)-2,5-di(thiophen-2-yl)-pyrrole (MPS), 1-(4-methoxyp...
A series of 4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-based conjugated polymers with 3,4-bis(d...
Thieno[3,2-b]thiophene (TT) monomers end-capped with 3,4-ethylenedioxythiophene (EDOT) moieties are ...
A series of diketopyrrolopyrrole (DPP) and propylenedioxythiophene (ProDOT)-containing random copoly...
A series of diketopyrrolopyrrole (DPP) and propylenedioxythiophene (ProDOT)-containing random copoly...
A centrosymmetric polymer precursor, namely 6-(2,5-di(thiophen-2-yl)-1H- pyrrol-1-yl)hexan-1-amine (...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
A centrosymmetric polymer precursor, namely 6-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)hexan-1-amine (T...
The development of semiconductor polymers for electronic applications requires tailored synthetic st...
The development of semiconductor polymers for electronic applications requires tailored synthetic st...
In this study, synthesis of a thiophene functionalized monomer, 1-benzyl-2,5-di(thiophene-2-yl)-1H-p...
In this study, synthesis of a thiophene functionalized monomer, 1-benzyl-2,5-di(thiophene-2-yl)-1H-p...
Three dithienylpyrroles (1-(4-(methylthio)phenyl)-2,5-di(thiophen-2-yl)-pyrrole (MPS), 1-(4-methoxyp...
Three dithienylpyrroles (1-(4-(methylthio)phenyl)-2,5-di(thiophen-2-yl)-pyrrole (MPS), 1-(4-methoxyp...
A series of 4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-based conjugated polymers with 3,4-bis(d...
Thieno[3,2-b]thiophene (TT) monomers end-capped with 3,4-ethylenedioxythiophene (EDOT) moieties are ...
A series of diketopyrrolopyrrole (DPP) and propylenedioxythiophene (ProDOT)-containing random copoly...
A series of diketopyrrolopyrrole (DPP) and propylenedioxythiophene (ProDOT)-containing random copoly...
A centrosymmetric polymer precursor, namely 6-(2,5-di(thiophen-2-yl)-1H- pyrrol-1-yl)hexan-1-amine (...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
Conducting polymers have attracted attention as active materials for low power consuming, flexible d...
A centrosymmetric polymer precursor, namely 6-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)hexan-1-amine (T...
The development of semiconductor polymers for electronic applications requires tailored synthetic st...
The development of semiconductor polymers for electronic applications requires tailored synthetic st...
In this study, synthesis of a thiophene functionalized monomer, 1-benzyl-2,5-di(thiophene-2-yl)-1H-p...
In this study, synthesis of a thiophene functionalized monomer, 1-benzyl-2,5-di(thiophene-2-yl)-1H-p...
Three dithienylpyrroles (1-(4-(methylthio)phenyl)-2,5-di(thiophen-2-yl)-pyrrole (MPS), 1-(4-methoxyp...
Three dithienylpyrroles (1-(4-(methylthio)phenyl)-2,5-di(thiophen-2-yl)-pyrrole (MPS), 1-(4-methoxyp...
A series of 4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-based conjugated polymers with 3,4-bis(d...
Thieno[3,2-b]thiophene (TT) monomers end-capped with 3,4-ethylenedioxythiophene (EDOT) moieties are ...