Abstract:Obtaining a wide color gamut and controllable color switching of electrochromic polymers (ECPs) is crucial for advanced applications. In this study we present a full-color palette of ECPs based on...
“…After reduction to diamine monomers 1-NH 2 and 2-NH 2 , the characteristic absorption bands of the nitro group disappeared, and the primary amino group characteristic bands appeared at 3454/ 3371 and 3442/3359 cm −1 (N−H stretching), respectively. The 1 H and 13 C NMR spectra of monomers are illustrated in Figure 1 and Figures S3−S10 and agree well with the proposed molecular structures. The signals at 4.78 and 5.61 ppm are assigned to the amino groups of monomers 1-NH 2 and 2-NH 2 , respectively (Figures S7a and S8a).…”
Section: Electrochemical and Spectroelectrochemical Characterizationsupporting
Section: Synthesis Of 44′-bis[(24-dimethoxyphenyl)(4nitrophenyl)amino...mentioning
confidence: 99%
“…However, inorganic EC materials are limited in manifesting diverse colors and coloring adjustments. Organic materials such as conducting polymers and viologens have recently become an intensive research topic. − The conducting polymers have several advantages over inorganic compounds as EC materials, including good electrochemical stability, fast switching speed, high coloring efficiency (CE), easy large-area processing, and color tuning through chemical modification. Also, triphenylamine (TPA)-containing polymers have been developed as an attractive family of EC materials because of their colorless neutral state and intriguing EC behaviors. − In recent years, redox-active materials with optical absorption change in the near IR (NIR) region have drawn significant attention due to their potential applications in optical communication, data storage, and thermal control in buildings and spacecraft. ,− For example, Wan et al reported that the quinone-containing EC materials revealed high absorption in NIR upon electrochemical reduction .…”
Section: Introductionmentioning
confidence: 99%
“…and13 C NMR spectra, ESI mass spectra, TMA, DMA, electrochemical properties, and single-crystal information (PDF) h i b i t e d .…”
Two polyamides (PAs) (PA1 and PA2) with
three electroactive nitrogen atoms within triphenylamine (TPA)-containing
structures were synthesized from two diamine monomers, 4,4′--bis[(2,4-dimethoxyphenyl)(4-aminophenyl)amino]-2″,4′′-dimethoxytriphenylamine
(1-NH2
) or 4,4′-bis(4-aminophenyl(4-methylphenyl)amino)-4′-methyltriphenylamine
(2-NH2
), and dicarboxylic acids via a phosphorylation
polyamidation technique. PA1 exhibited highly integrated
electrochromic performances, including multiple color changes (colorless
to grass green, green, and blue), fast response speed (7.7/2.6 s at
422 nm for the first electrochromic process), high contrast of optical
transmittance change (ΔT = 54% at 422 nm at
the first oxidation stage), and excellent electrochromic stability.
Introducing electron-donating ortho and para methoxy substituents and three electroactive nitrogen centers could
effectively increase the electrochromic stability of the resulting PA1. At the first oxidation stage, PA1 exhibited
the highest electrochromic stability (only 4.1 and 2.5% decay of its
coloration efficiency (CE) at 422 and 1252 nm after 15,000 switching
cycles, respectively) compared to all other TPA-based polymers. It
was noteworthy for the first time that the polymers containing more
electroactive nitrogen centers reveal longer wavelength absorption
in the near-infrared (NIR) region at the first oxidation stage due
to cation radical delocalization. The delocalization could facilitate
electrochromic stability, and the relationship between the structures
and electrochromic stability for these TPA-based polymers was also
investigated. In addition, these PAs exhibited good solubility in
many solvents and could be solution-cast into flexible films. They
showed good thermal stability with glass transition temperatures ranging
from 236 to 278 °C and 10% weight loss in nitrogen at temperatures
above 425 °C.
“…After reduction to diamine monomers 1-NH 2 and 2-NH 2 , the characteristic absorption bands of the nitro group disappeared, and the primary amino group characteristic bands appeared at 3454/ 3371 and 3442/3359 cm −1 (N−H stretching), respectively. The 1 H and 13 C NMR spectra of monomers are illustrated in Figure 1 and Figures S3−S10 and agree well with the proposed molecular structures. The signals at 4.78 and 5.61 ppm are assigned to the amino groups of monomers 1-NH 2 and 2-NH 2 , respectively (Figures S7a and S8a).…”
Section: Electrochemical and Spectroelectrochemical Characterizationsupporting
Section: Synthesis Of 44′-bis[(24-dimethoxyphenyl)(4nitrophenyl)amino...mentioning
confidence: 99%
“…However, inorganic EC materials are limited in manifesting diverse colors and coloring adjustments. Organic materials such as conducting polymers and viologens have recently become an intensive research topic. − The conducting polymers have several advantages over inorganic compounds as EC materials, including good electrochemical stability, fast switching speed, high coloring efficiency (CE), easy large-area processing, and color tuning through chemical modification. Also, triphenylamine (TPA)-containing polymers have been developed as an attractive family of EC materials because of their colorless neutral state and intriguing EC behaviors. − In recent years, redox-active materials with optical absorption change in the near IR (NIR) region have drawn significant attention due to their potential applications in optical communication, data storage, and thermal control in buildings and spacecraft. ,− For example, Wan et al reported that the quinone-containing EC materials revealed high absorption in NIR upon electrochemical reduction .…”
Section: Introductionmentioning
confidence: 99%
“…and13 C NMR spectra, ESI mass spectra, TMA, DMA, electrochemical properties, and single-crystal information (PDF) h i b i t e d .…”
Two polyamides (PAs) (PA1 and PA2) with
three electroactive nitrogen atoms within triphenylamine (TPA)-containing
structures were synthesized from two diamine monomers, 4,4′--bis[(2,4-dimethoxyphenyl)(4-aminophenyl)amino]-2″,4′′-dimethoxytriphenylamine
(1-NH2
) or 4,4′-bis(4-aminophenyl(4-methylphenyl)amino)-4′-methyltriphenylamine
(2-NH2
), and dicarboxylic acids via a phosphorylation
polyamidation technique. PA1 exhibited highly integrated
electrochromic performances, including multiple color changes (colorless
to grass green, green, and blue), fast response speed (7.7/2.6 s at
422 nm for the first electrochromic process), high contrast of optical
transmittance change (ΔT = 54% at 422 nm at
the first oxidation stage), and excellent electrochromic stability.
Introducing electron-donating ortho and para methoxy substituents and three electroactive nitrogen centers could
effectively increase the electrochromic stability of the resulting PA1. At the first oxidation stage, PA1 exhibited
the highest electrochromic stability (only 4.1 and 2.5% decay of its
coloration efficiency (CE) at 422 and 1252 nm after 15,000 switching
cycles, respectively) compared to all other TPA-based polymers. It
was noteworthy for the first time that the polymers containing more
electroactive nitrogen centers reveal longer wavelength absorption
in the near-infrared (NIR) region at the first oxidation stage due
to cation radical delocalization. The delocalization could facilitate
electrochromic stability, and the relationship between the structures
and electrochromic stability for these TPA-based polymers was also
investigated. In addition, these PAs exhibited good solubility in
many solvents and could be solution-cast into flexible films. They
showed good thermal stability with glass transition temperatures ranging
from 236 to 278 °C and 10% weight loss in nitrogen at temperatures
above 425 °C.
“…They should have the characteristics of total reflection of light in the colorless state and full absorption of the visible spectrum in the black state [ 21 ]. Most of the black electrochromic materials are designed based on the color mixing theory; that is, the polymer is introduced with chromophore groups with different absorption wavelengths, and the material absorbs the visible spectrum by adjusting the proportion of different chromophore groups, thereby achieving the black display effect [ 66 , 67 , 68 , 69 ]. However, such designs typically result in polymers having a higher operating voltage, which is an important factor leading to polymer instability.…”
Section: Special Engineering Plastic-based Electrochromic Polymers (S...mentioning
SPECPs are electrochromic polymers that contain special engineering plastic structural characteristic groups (SPECPs). Due to their high thermal stability, mechanical properties, and weather resistance, they are also known as high-performance electrochromic polymer (HPEP or HPP). Meanwhile, due to the structural characteristics of their long polymer chains, these materials have natural advantages in the application of flexible electrochromic devices. According to the structure of special engineering plastic groups, SPECPs are divided into five categories: polyamide, polyimide, polyamide imide, polyarylsulfone, and polyarylketone. This article mainly introduces the latest research on SPECPs. The structural design, electrochromic properties, and applications of these materials are also introduced in this article, and the challenges and future development trends of SPECPs are prospected.
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