Ternary Polymer Research Articles

Ternary Polymer Solar Cells: Impact of Non-Fullerene Acceptors on Optical and Morphological Properties

Ternary organic solar cells contain a single three-component photoactive layer with a wide absorption window, achieved without the need for multiple stacking. However, adding a third component into a well-known binary blend can influence the energetics, optical window, charge carrier transport, crystalline order and conversion efficiency. In the form of binary blends, the low-bandgap regioregular polymer donor poly(3-hexylthiophene-2,5-diyl), known as P3HT, is combined with the acceptor PC61BM, an inexpensive fullerene derivative. Two different non-fullerene acceptors (ITIC and eh-IDTBR) are added to this binary blend to form ternary blends. A systematic comparison between binary and ternary systems was carried out as a function of the thermal annealing temperature of organic layers (100 °C and 140 °C). The power conversion efficiency (PCE) is improved due to increased fill factor (FF) and open-circuit voltage (Voc) for thermal-annealed ternary blends at 140 °C. The transport properties of electrons and holes were investigated in binary and ternary blends following a Space-Charge-Limited Current (SCLC) protocol. A favorable balanced hole–electron mobility is obtained through the incorporation of either ITIC or eh-IDTBR. The charge transport behavior is correlated with the bulk heterojunction (BHJ) morphology deduced from atomic force microscopy (AFM), contact water angle (CWA) measurement and 2D grazing-incidence X-ray diffractometry (2D-GIXRD).

Adsorption and antibacterial studies of a novel hydrogel adsorbent based on ternary eco-polymers doped with sulfonated graphene oxide developed from upcycled plastic waste

A novel ternary blended polymer composed of cost-effective and readily available polymers was synthesized using poly (vinyl alcohol) (PVA), iota carrageenan (IC), and poly (vinyl pyrrolidone) (PVP). Sulfonated graphene oxide (SGO), prepared from recycled drinking water bottles, was utilized as a doping agent. Varying amounts (1–3 wt%) were combined into the polymer matrix. The produced hydrogel film was examined as a potential adsorbent hydrogel film for the removal of methylene blue (MB) and Gentamicin sulfate (GMS) antibiotic from an aqueous solution. The experimental results demonstrate that the presence of SGO significantly increased the adsorption efficiency of PVA/IC/PVP hydrogel film. The antimicrobial tests revealed that the PVA/IC/PVP-3% SGO hydrogel film exhibited the most potent activity against all the tested pathogenic bacteria. However, the adsorption results for MB and GMS showed that the addition of 3 wt% SGO resulted in a removal percentage that was a two fold increase in the removal percentage compared with the undoped PVA/IC/PVP hydrogel film. Furthermore, the response surface methodology (RSM) model was utilized to examine and optimize several operating parameters, including time, pH of the solution, and initial pollutant concentration. The adsorption kinetics were better characterized by the pseudo-second-order kinetics model. The composite film containing 3 wt% SGO had a maximum adsorption capacity of 606 mg g−1 for MB and 654 mg g−1 for GMS, respectively. The generated nanocomposite hydrogel film demonstrated promising potential for application in water purification systems.

Ternary Solid Polymer Electrolytes at the Electrochemical Interface: A Computational Study.

Polymer-based solid-like gel electrolytes have emerged as a promising alternative to improve battery performance. However, there is a scarcity of studies on the behavior of these media at the electrochemical interface. In this work, we report classical MD simulations of ternary polymer electrolytes composed of poly(ethylene oxide), a lithium salt [lithium bis(trifluoromethanesulfonyl)imide], and different ionic liquids [1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide and 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide] confined between two charged and uncharged graphene-like surfaces. The molecular solvation of Li+ ions and their diffusion as well as the polymer conformational picture were characterized in terms of the radial distribution functions, coordination numbers, number density profiles, orientations, displacement variance, polymer radius of gyration, and polymer end-to-end distance. Our results show that the layering behavior of the ternary electrolyte in the interfacial region leads to a decrease of Li+ mobility in the direction perpendicular to the electrodes and high energy barriers that hinder lithium cations from coming into direct contact with the graphene-like surface. The nature of the ionic liquid and its concentration were found to influence the structural and dynamic properties at the electrode/electrolyte interface, the electrolyte with low amounts of the pyrrolidinium-based ionic liquid being that with the best performance since it favors the migration of Li+ cations toward the negative electrode when compared to the imidazolium-based one.

Solution-Processed Ternary Perovskite-Conjugated Polymer Photodetector with a Photoresponse up to 1200 nm

Solution-Processed Ternary Perovskite-Conjugated Polymer Photodetector with a Photoresponse up to 1200 nm

Dual-Aptamer Recognition of DNA Logic Gate Sensor-Based Specific Exosomal Proteins for Ovarian Cancer Diagnosis.

Clinical diagnosis of ovarian cancer lacks high accuracy due to the weak selection of specific biomarkers along with the circumstance biomarkers localization. Clustering analysis of proteins transported on exosomes enables a more precise screening of effective biomarkers. Herein, through bioinformatics analysis of ovarian cancer and exosome proteomes, two coexpressed proteins, EpCAM and CD24, specifically enriched, were identified, together with the development of an as-derived dual-aptamer targeted exosome-based strategy for ovarian cancer screening. In brief, a DNA ternary polymer with aptamers targeting EpCAM and CD24 was designed to present a logic gate reaction upon recognizing ovarian cancer exosomes, triggering a rolling circle amplification chemiluminescent signal. A dynamic detection range of 6 orders of magnitude was achieved by quantifying exosomes. Moreover, for clinical samples, this strategy could accurately differentiate exosomes from healthy persons, other cancer patients, and ovarian cancer patients, enabling promising in situ detection. By accurately selecting biomarkers and constructing a dual-targeted exosomal protein detection strategy, the limitation of insufficient specificity of traditional protein markers was circumvented. This work contributed to the development of exosome-based prognosis monitoring in ovarian cancer through the identification of disease-specific exosome protein markers.

Engineering properties of hybrid polymer composites produced with different unsaturated polyesters and hybrid epoxy

In this study, the mechanical properties of hybrid polymer composites produced with different unsaturated polyesters and hybrid epoxy resins are investigated. The composites were produced by blending unsaturated polyester resins (i.e., orthophthalic, isophthalic, and terephthalic) and bisphenol-A-based epoxy-vinyl ester resin to produce single, binary and ternary blends. In doing this, a total of 14 different combinations were produced. The results show that the binary and ternary polymer blends tend to improve almost all the tested properties of the polymer composites. Further, the fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) results confirmed that the reason for enahcned properties is due to better crosslinking and longer chains of polymers produced in binary and ternary mixtures. The absence of peaks determining the styrene polymerization character for all mixtures also demonstrates that the polymerization reaction takes place in all mixtures. It is also believed that the binary and ternary resin mixtures have developed higher energy absorption compared to single resin composites. All of the mentioned has been achieved while the gelation temperatures of the hybrid resin mixtures were not changed significantly and they began gelation at the expected temperature values. In addition to the gelation, peak exotherm temperatures, and barcol hardness values demonstrated that all mixtures achieved sufficient curing. The result of this study is significant and point to the great potential of producing high performance polymer composites through the use of binary or ternary resin mixtures.

Constructing the Polymer Molecules to Regulate the Electrode/Electrolyte Interface to Enhance Lithium-Metal Battery Performance.

Lithium-ion batteries, with high energy density and long cycle life, have become the battery of choice for most vehicles and portable electronic devices; however, energy density, safety and cycle life require further improvements. Single-functional group electrolyte additives are very limited in practical applications, a ternary polymer bifunctional electrolyte additive copolymer (acrylonitrile-butyl hexafluoro methacrylate- poly (ethylene glycol) methacrylate- methyl ether) (PMANHF) was synthesized by free radical polymerization of acrylonitrile, 2, 2, 3, 4, 4, 4-hexafluorobutyl methacrylate and poly (ethylene glycol) methyl ether methacrylate. A series of characterizations show that in Li metal anodes, the preferential reduction of PMANHF is conducive to the formation of a uniform and stable solid electrolyte interphase layer, and Li deposition is uniform and dense. At the NCM811 cathode, a film composed of LiF- and Li3N-rich is formed at the cathode-electrolyte interface, mitigating the side reaction at the interface. At 1.0 mA cm-2, the Li/Li cell can be stabilized for 1000 cycles. In addition, the Li/NCM811 cell can stabilize 200 cycles with a cathode capacity of 153.7 mAh g-1, with the capacity retention of 89.93 %, at a negative/positive capacity ratio of 2.5. This study brings to light essential ideas for the fabrication of additives for lithium-metal batteries.

High-Efficiency Ternary Polymer Solar Cells with a Gradient-Blended Structure Fabricated by Sequential Deposition.

Acquiring the ideal blend morphology of the active layer to optimize charge separation and collection is a constant goal of polymer solar cells (PSCs). In this paper, the ternary strategy and the sequential deposition process were combined to make sufficient use of the solar spectrum, optimize the energy-level structure, regulate the vertical phase separation morphology, and ultimately enhance the power conversion efficiency (PCE) and stability of the PSCs. Specifically, the donor and acceptor illustrated a gradient-blended distribution in the sequential deposition-processed films, thus resulting in facilitated carrier characteristics in the gradient-blended devices. Consequently, the PSCs based on D18-Cl/Y6:ZY-4Cl have achieved a device efficiency of over 18% with the synergetic improvement of open-circuit voltage (VOC), short-circuit current density (JSC), and fill factor (FF). Therefore, this work reveals a facile approach to fabricating PSCs with improved performance and stability.

Tuning low frequency dielectric properties of flexible ternary polymer blend film reinforced with bio- ionic liquid for the application in green electronics

Biofriendly conducting polymeric blends and composites exhibiting high dielectric constant and dielectric loss are promising for applications as sensors, actuators, microwave absorbing materials, fuel cells and biomedical applications. A great deal of work is reported on using fillers such as conductive nanomaterials, bio ceramics, carbon nanotubes, graphene etc in blends of Polyvinylchloride, Polyvinylpyrrolidone, Polymethylmethacrylate, Polyvinyl alcohol with conducting polymer Polypyrrole, Polyaniline for enhancing their conductivities, tailoring dielectric and electrical, thermal and surface properties of such polymeric materials. However, appropriate dispersion of such fillers in polymeric matrices remains technically challenging. In this regard, bio-ionic liquids have emerged as a novel class of materials and their combination with specific polymer blends opens the possibility to develop smart novel materials with different morphologies. Present work aims to explore the low frequency dielectric properties exhibited by free standing, flexible, biofriendly/biodegradable ternary polymer blend film of Polyvinylchloride-Polyvinylpyrrolidone-Polypyrrole reinforced with choline acetate. The detailed analysis of low frequency dielectric properties authenticates that addition of choline acetate result in modifying the dielectric properties of ternary polymer blend film.. The harmlessness of these films was confirmed from disk diffusion test indicating their benign nature towards (Escherichia coli) (CFT073) and (Bacillus subtilis). Therefore, the developed films can potentially be used for various scale multifunctional dielectric and electrical applications working in close contact with living matter, green electronics and various health monitoring systems.

Efficient triisopropylsilylethynyl-substituted benzo[1,2-b:4,5-b′]dithiophene-based random terpolymers enable non-fullerene organic solar cells with enhanced efficiency

Recent work has highlighted the pivotal role of ternary random polymers in the development of efficient high-performance polymer donors for organic solar cells (OSCs) and most of these D-A copolymer donors are so far constituted of an equal proportion of D and A-units. In this contribution, we report series of PM6-based ternary random terpolymers with unequal D- and A-units, namely, PM-TIPS10, PM-TIPS20 and PM-TIPS20, respectively by adding the 10%, 20% and 30% of simple and low-cost triisopropylsilylethynyl-substituted benzo[1,2-b:4,5-b′]dithiophene (BDT-TIPS) unit as second donor (D1) unit in polymer backbone based on D1-A-D2-A molecular design. Ascribed from the structural similarity of the two building blocks in the terpolymer backbone, these polymers showed orderly molecular packing, broadened light absorption, and the face-on orientation of the active layer to facilitate charge transport. Additionally, the new polymers displayed much deeper highest occupied molecular orbital (HOMO) energy levels than host PM6 polymer, which helped in enhancing the open circuit voltage (Voc) in the PM-TIPS-based OSCs. As a result, when combined with BTP-eC9 acceptor unit, PM-TIPS10 and PM-TIPS20 displayed best efficiency of 16.7 and 16.5% with a small energy loss of 0.484 and 0.473 eV, producing overall superior device parameters compared to PM6-based devices tested parallelly (PCE of 15.7%). This study reveals the correlation between introduction of the BDT-TIPS unit on polymer properties and photovoltaic performance and thus contributes to the design of high-PCE polymer donors by adapting a ternary random copolymerization strategy.

A review of ternary polymer nanocomposites containing clay and calcium carbonate and their biomedical applications

Abstract Patchy interactions and heterogeneous charge distribution make nanoclay (NC) a promising biomaterial to interact with different biomolecules, polymers, and biological components. Many researchers have studied the polymer/clay nanocomposites in recent years. However, some deficiencies, such as poor impact strength, limit the application of polymer/clay nanocomposites in different fields. As a result, many attempts have been made to resolve this problem. Also, researchers have developed calcium carbonate (CaCO3) nanoparticles as biomedical materials. The nontoxic properties and biocompatibility of both CaCO3 and NC make their nanocomposites ideal for biomedical applications. In this article, a detailed review of the ternary polymer nanocomposites containing NC and CaCO3 is presented. The morphological, thermal, mechanical, and rheological characteristics, in addition to the modeling of behavior and foam properties, are studied in this article. In addition, the potential challenges for ternary nanocomposites and their biomedical applications are discussed.

High‐Performance Terpolymers with Well‐Defined Structures Facilitate PCE Over 19% for Polymer Solar Cells

AbstractTernary copolymerization is a cost‐effective and time‐saving approach to improve device performance and batch stability of polymer donors. However, the structure of the ternary polymer donor obtained by the traditional one‐pot polymerization is vague due to the different monomer reaction order, which has a great influence on the absorption, crystallization, molecular stacking, and device performance. Therefore, it is necessary to obtain terpolymers with definite structures, and systematically study the differences in device properties of polymers with different sequence structures. Herein, three terpolymers D1, D2, and D3 are developed. Random copolymer D3 is obtained via the traditional one‐pot method while alternating copolymer donor D1 and block copolymer D2 are synthesized by stepwise polymerization. Because the block copolymer D2 possess periodic sequence distribution and retains the excellent properties of the two polymer matrix very well, the D2‐based device shows enhanced tightened π‐face‐on molecular stacking, distinguished efficient exciton dissociation, and decreased energy loss. As a result, the D2:L8‐BO‐based polymer solar cells achieve one of a record power conversion efficiency of 19.03%. The work demonstrates changing the sequence structure of the polymers to synthesize well‐defined structures polymer donors not only maintains the features of polymer matrix, but also combines the advantages of ternary copolymerization.

General Entropy Approach Toward Ultratough Sustainable Plastics.

Entropy is a universal concept across the physics of mixtures. While the role of entropy in other multicomponent materials has been appreciated, its effects in polymers and plastics have not. In this work, it is demonstrated that the seemingly small mixing entropy contributes to the miscibility and performance of polymer alloys. Experimental and modeling studies on over 30 polymer pairs reveal a strong correlation between entropy, morphology, and mechanical properties, while elucidating the mechanism behind: in polymer blends with weak interactions, entropy leads to homogeneously dispersed nanosized domains stabilized by highly entangled chains. This unique microstructure promotes uniform plastic deformation at the interface, thus improving the toughness of conventional brittle polymers by 1-2 orders of magnitude without sacrificing other properties, analogous to high-entropy metallic alloys. The proposed strategy also applies to ternary polymer systems and copolymers, offering a new pathway toward the development of sustainable polymers.

Hydrophobic polymer nano hybrid ternary composite electrode for nanomolar tracing of Cd2+ ions

AbstractIn the present study, we reported the successful synthesis of a ternary nano hybrid polymer composite system obtained by solution casting. Composing carbon nanotubes (CNTs) and molybdenum disulfide (MoS2) in ethylene vinyl acetate (EVA) derived ECM ternary electrode. It demonstrated an excellent electrochemical sensor performance and a more efficient supercapacitor. Chemical structure of hybrid electrode Fourier transform Infrared Spectroscopy (FTIR) illustrated the CS and CN stretching with MoS2 and CNT new bands (at 1368 and 1032 cm−1). FE‐SEM and Atomic force microscopy (AFM) 3D topographic image identified the decreased rough morphology of the hybrid electrode. Whereas contact angle measurements revealed the enhanced wettability of electrode system. Microporous nature of the hybrid electrode was observed through SEM investigation. Transmission electron microscopy (TEM) revealed the nano hybrid entity in a hybrid electrode system. XRD and TEM investigation confirmed semicrystalline phase of the hybrid electrode system due to the presence of MoS2. D band, G bands, E12g and A1g vibrational modes in Raman spectroscopy revealed the occupied hybrid filler CNTs and MoS2. An electroactive site for the Cd2+ ion sensor was confirmed by the ECM/PGE hybrid electrode. It comply the desirable sensor qualities, such as excellent selectivity, reproducibility and repeatability with a high accuracy and lower detection limit of 15 nM. Additionally, the ECM/PGE electrode demonstrated a capacitive nature with an aerial capacitance of 73 μF/cm2 at an applied current density of 3 μA/cm2. Furthermore, it exhibited a power density of 44 mW/cm2 and an energy density of 148 μWh/cm2 over a wide potential range of 1 V.

Mechanical Properties, Morphological Characterization and Melt Dripping Studies of Polypropylene (PP) + High Density Polyethylene (HDPE) + Polystyrene (PS) Ternary Polymer Blends: Non-Isothermal Degradation Kinetics of Compatibilized and Uncompatibilized Blends

Polymer composites have been widely used due to its light weight, performance with good mechanical properties, corrosion resistant, solvent resistance and it becomes an important part of the industries. Polypropylene (PP), polystyrene (PS) and high-density polyethylene (HDPE) are applied to various commercial as well as automobile spare parts. In this study PP, PS and HDPE were melt mixed together to form a ternary polymer blend and mechanical, morphological, thermogravimetric analysis were conducted to determine its potential applications. The compatibilization of the blend was achieved by the combination of ethylene-propylenediene- monomer (EPDM) and styrene-ethylene-butylene-styrene (SEBS). Model free methods like Flynn Wall Ozawa (FWO), Kissinger-Akahira- Sunose equation (KAS) and Friedman methods were applied to estimate the activation energy values at different heating rates of 5, 10 and 15 ºC/min. The compatibilized blend of 80PP/5PS/15HDPE with 5% SEBS/EPDM showed better tensile strength compared to uncompatibilized. Freidman method produced a higher value of average activation energy as 203.4 kJ/mol. The melt dripping characteristics was also analyzed were the time to ignition and time for first drip was found to be in the range of 6 to 9 s and 14-16 s. Pure and compatibilized blends showed a very low limiting oxygen index (LOI) values as in the range of 18.7 to 18.9. Elastomeric/rubber blend compatibilization was achieved and the material can be applied to light weight automobile applications. From morphological characterization, it was understood that compatibilized blends are more durable and easily transfer the stress uniformly through the interface. This compatibilized blend can also be used in low temperature regions.

Mimicking Charged Host-Defense Peptides to Tune the Antifungal Activity and Biocompatibility of Amphiphilic Polymers.

Invasive fungal infections impose a substantial global health burden. They cause more than 1.5 million deaths annually and are insufficiently met by the currently approved antifungal drugs. Antifungal peptides are a promising alternative to existing antifungal drugs; however, they can be challenging to synthesize, and are often susceptible to proteases in vivo. Synthetic polymers which mimic the properties of natural antifungal peptides can circumvent these limitations. In this study, we developed a library of 29 amphiphilic polyacrylamides with different charged units, namely, amines, guanidinium, imidazole, and carboxylic acid groups, representative of the natural amino acids lysine, arginine, histidine, and glutamic acid. Ternary polymers incorporating primary ammonium (lysine-like) or imidazole (histidine-like) groups demonstrated superior activity against Candida albicans and biocompatibility with mammalian cells compared to the polymers containing the other charged groups. Furthermore, a combination of primary ammonium, imidazole, and guanidinium (arginine-like) within the same polymer outperformed the antifungal drug amphotericin B in terms of therapeutic index and exhibited fast C. albicans-killing activity. The most promising polymer compositions showed synergistic effects in combination with caspofungin and fluconazole against C. albicans and additionally demonstrated activity against other clinically relevant fungi. Collectively, these results indicate the strong potential of these easily producible polymers to be used as antifungals.

Reference-free quantitative mass spectrometry in the presence of nonlinear distortion caused by in situ chemical reactions among constituents.

Materials performance is primarily influenced by chemical composition, making compositional analysis (CA) essential in materials science. Traditional quantitative mass spectrometry, which deconvolutes analyte spectra into reference spectra, struggles with reactive systems where spectral variations occur, such as peak shifts and new peak emergences. Additionally, obtaining reference spectra for all pure constituents is often impractical. To address these challenges, I propose nonlinear reference-free quantitative mass spectrometry (NL-RQMS). This method simultaneously determines composition, reference spectra, and nonlinear interaction effects directly from a spectral dataset of mixtures, eliminating the need for prior reference spectra. In a benchmark test on ternary reactive polymers of epoxy and amines, NL-RQMS inferred compositions with an error margin of just 3 wt%, significantly outperforming the 6 wt% error margin of linear RQMS. The inferred interaction terms clearly indicate in situ reactions between epoxy and amine moieties. This framework enables accurate compositional analysis without prior knowledge of the constituents, even in systems with interactive components, and holds significant potential for applications such as grading recycled plastics, where pristine materials, degradation compounds, and stabilizers interact complexly, causing nonlinear spectral distortions.

Thermogravimetry-synchronized, reference-free quantitative mass spectrometry for accurate compositional analysis of polymer systems without prior knowledge of constituents.

Compositional analysis (CA)-identification and quantification of the system constituents-is the most fundamental and decisive approach for investigating the system of interest. Pyrolysis mass spectrometry (MS) with a high resolution of over 10 000 is very effective for chemical identification and is directly applicable to polymer materials regardless of their solubilities. However, it is less helpful for quantification, especially when the references, i.e., pure constituents, are unknown, non-isolable and thus cannot be prepared. To compensate for this weakness, herein we propose reference-free quantitative mass spectrometry (RQMS) with enhanced quantification accuracy assisted by synchronized thermogravimetry (TG). The key to success lies in correlating the instantaneous weight loss from TG with the MS signal, enabling the quantitative evaluation of the distinct ionization efficiency for each fragment individually. The determined ionization efficiencies allow the conversion of MS signal intensities of pyrolyzed fragments into weight abundances. In a benchmark test using ternary polymer systems, this new framework named TG-RQMS demonstrates accurate CA within ±1.3 wt% errors without using any prior knowledge or spectra of the references. This simple yet accurate and versatile CA method would be an invaluable tool to investigate polymer materials whose composition is hardly accessible via other analytical methods.

Investigation of Thermal, Microstructure and Shape Memory Behavior of PLA-PEG-PHA Ternary Polymer Blends

Instead of blending two polymers to make a blend, a "ternary polymer blend" is typically created by adding a third polymer. In recent years, triple polymer blends have found a wide field of study in order to improve and change the properties of traditionally obtained binary blends. In this study, a blend was created by adding Polyhydroxy Alkanoate (PHA) polymer to Polylactic Acid (PLA) and Polyethylene Glycol (PEG) polymers, which are known to be compatible with each other. The aim of this study is to examine the effect of changing PHA amount on the blend of the triple shape memory alloy. The thermal properties, shape memory and scanning electron microscope (SEM) images of this blending were examined. It was investigated which of the samples prepared with three different percentages would give the most ideal results. Although the thermal analysis results are generally close to each other, differences were observed in the shape memory of the material due to the change in the amount. In particular, it can be said that the decrease in the percentage of Polytactic Acid (PLA) polymer, which has binding properties, causes a delay in shape transformation.

Fine-tuning the color hue of the solution-processable electrochromic copolymers based on the diketopyrrolopyrrole, benzodithiophene and dithienosilole units

Electrochromic materials (ECMs) have attracted increasing attentions on account of their extensive prospects and numerous demands. Here, the classical donor-acceptor (D-A) alternative copolymerization strategy was used to synthesize three kinds of novel conjugated polymers PBPS-1, PBPS-2, and PBPS-3. The diketopyrrolopyrrole (M1) unit with a long alkyl side-chain was employed as the core acceptor while the dithienosilole (M2) used as the donor units. More importantly, the benzodithiophene (M3) units which have the high skeleton coplanarity was selected as the bridge units to enhance the charge transport. Variations of the feed ratios of monomers was used to regulate the energy level and spectral absorption range of the solid films. Three polymers exhibited the abundant color hues in the redox process, which including grape purple/brownness/aircraft ash color (PBPS-1), dark grey/red soap/dusty blue color (PBPS-2) and marine blue/grayish/celadon color (PBPS-3). Electrochromic performances demonstrated that PBPS-2 possessed the fast discoloration speed as low as 0.26 s and the outstanding coloration efficiency (550.1 cm2·C−1), which portended a valuable material for smart ECMs applications. Furthermore, the effect of different feed ratios for three polymer in electrochemical, optical and kinetic properties were investigated in detail, which showed the satisfactory optical contrasts (>70% in the NIR region) and good kinetic stability (>97% retention in 1000 s). In general, this exploration supplied a handy design strategy for fine tuning of polymer color and conducive to strengthen the understanding of EC behaviors of the ternary polymers, which deserve further researches to explore more promising ECMs.