Abstract

Four copolymers (P(tCz (tris(4-carbazoyl-9-ylphenyl)amine)-co-bTP (2,2′-bithiophene)), P(tCz-co-CPDT (4H-cyclopenta[2,1-b:3,4-b’]dithiophene)), P(tCz-co-DTC (3,6-di(2-thienyl)carbazole)), and P(tCz-co-CPDTK (cyclopentadithiophene ketone))) are deposited on indium tin oxide (ITO) surfaces using electrochemical polymerization. Spectroelectrochemical properties of copolymer electrodes reveal that the colors of P(tCz-co-bTP) film are pinkish-orange, light olive green, light grayish blue, and dark blue at 0.0, 0.8, 1.2, and 1.6 V, respectively, whereas the color variations of P(tCz-co-CPDTK) film are light yellow, yellow, and blue at 0.0 V, 0.8 V, and 1.5 V, respectively. The ΔT of P(tCz-co-bTP), P(tCz-co-CPDT), P(tCz-co-DTC), and P(tCz-co-CPDTK) films are estimated to be 43.0% at 967 nm, 28.7% at 864 nm, 43.6% at 870 nm, and 24.5% at 984 nm, respectively. Five electrochromic devices (ECDs) are assembled using the tCz-based homopolymer and copolymers as coloring electrodes, and poly(2,2-dimethyl-3,4-propylenedioxythiophene) (PProDOT-Me2) as the complementary electrode. P(tCz-co-DTC)/PProDOT-Me2 ECD reveals high transmittance change (45.9% at 624 nm), P(tCz-co-CPDTK)/PProDOT-Me2 ECD shows high η (513.0 cm2 C−1 at 582 nm), and P(tCz-co-bTP)/PProDOT-Me2 ECD presents short switching time (less than 0.4 s) at 628 nm. Moreover, these ECDs show satisfactory redox stability and open circuit stability.

Highlights

  • Electrochromic materials (ECMs) have attracted attention in the scientific communities due to their advantage of low driving voltage and high contrast of transmittance [1]

  • (cyclopentadithiophene ketone))) are copolymerized electrochemically to study their promising applications as ECMs. tCz contains three carbazole units linked by a triphenylamine core

  • At 0.0 V, PtCz, P(tCz-co-bTP), and P(tCz-co-DTC) films showed a bleached color in their neutral state and PProDOT-Me2 was transparent in its oxidized state

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Summary

Introduction

Electrochromic materials (ECMs) have attracted attention in the scientific communities due to their advantage of low driving voltage and high contrast of transmittance [1]. Copolymerization of various monomers containing specific functional groups can bring about interesting electrochromic behaviors For this matter, four carbazole- and bithiophene-containing copolymers (P(tCz-co-bTP (2,20 -bithiophene)), P(tCz-co-CPDT), P(tCz-co-DTC (3,6-di(2-thienyl)carbazole)), and P(tCz-co-CPDTK (cyclopentadithiophene ketone))) are copolymerized electrochemically to study their promising applications as ECMs. tCz contains three carbazole units linked by a triphenylamine core. All of bTP, CPDT, DTC, and CPDTK units comprise two thiophene rings linked by specific groups. The two thiophene rings of bTP and DTC units are linked by a single bond and a carbazole group, respectively. Five ECDs comprised of PtCz, P(tCz-co-bTP), P(tCz-co-CPDT), P(tCz-co-DTC), or P(tCz-co-CPDTK) as anodically coloring layer, and PProDOT-Me2 as cathodically coloring layer were constructed and their spectroelectrochemical behaviors, transmittance variations of electrochromic switching, optical memory, and redox stability were investigated

Materials
Electrochemical and Spectroelectrochemical Characterizations
Construction of Electrochromic Devices
Electrochemical Polymerization
Spectroelectrochemical Studies of Polymer Films
Electrochemical Switching of Polymer Films
Spectroelectrochemistry of ECDs
Electrochemical Switching of ECDs
Open Circuit Memory
Stability
Conclusions
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