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The significant progress of p‐type and n‐type active layer materials in the past several years has pushed the power conversion efficiency (PCE) of organic solar cells (OSCs) toward 19%. Due to the relatively low synthesis cost and simple synthesis method of carboxylate‐containing building blocks, including thiophene, thieno[3,2‐b]thiophene, thieno[3,4‐b]thiophene, furan, pyrazine, benzodithiophene, benzothiazole, quinoxaline, etc., are widely used to construct p‐type photovoltaic polymers. These resulting carboxylate‐bearing polymers present downward energy levels, high absorption coefficient, narrow bandgap, high hole mobility, and strong aggregation behavior, which have dabbled in the fabrication of mechanically stretchable, semitransparent, indoor, and tandem OSCs, etc., and produce excellent photovoltaic performance. The low‐cost carboxylate‐containing copolymers exhibit a satisfying PCE approaching 17%, and the random terpolymer systems achieve a high PCE over 19%. This review focuses on the progress of carboxylate‐containing photovoltaic polymers, summarizes the molecular characteristics, discusses their structure‐performance relationship, and offers a summary and outlook on the challenges for future molecular development. [ABSTRACT FROM AUTHOR]

The binary electron donor–electron acceptor (D‐A) type conjugated polymers have proven to be efficient dopant‐free hole‐transporting materials (HTMs) for the n‐i‐p perovskite solar cells (PVSCs). However, D‐A type terpolymeric HTMs containing two D units are not exploited. Reserving the high‐planarity backbone of benzodithiophene (BDT)‐benzodithiophene‐4,8‐dione, D1‐A‐D2‐A type terpolymers PT‐Cz30, PT‐Cz50, and PT‐Cz70 are obtained by side‐chain engineering and ternary copolymerization strategy, in which BDT bearing the side chains of thiophene and carbazole serves as D1 and D2 units, respectively. PT‐Cz50 performs best due to the appropriate side‐chain ratio around 1:1. Meanwhile, a polymer blend HTM PA‐Cz50 is studied for comparison, in which two binary D‐A polymers PBDB‐T and PBDB‐Cz are blended with the molar ratio of 1:1. Containing similar side‐chain composition, terpolymer PT‐Cz50 presents superior hole transport properties over the polymer blend PA‐Cz50 and endows better device performances to the PVSCs with a promising power conversion efficiency of 22.53% and high device stability. [ABSTRACT FROM AUTHOR]

In this work, polymeric materials designed for enhanced oil recovery (EOR) were evaluated for their intended application. Properties including viscosity, flow through porous media (resistance factor and residual resistance factor), and heavy oil displacement (incremental oil recovery) were assessed for designed terpolymers of 2‐acrylamido‐2‐methylpropane sulphonic acid (AMPS), acrylamide (AAm), and acrylic acid (AAc). The same properties were evaluated for two commercially available reference materials (e.g., partially hydrolyzed polyacrylamides or HPAM) with similar characteristics, which allowed for direct comparison between the newly designed terpolymers and materials that are currently on the market for the polymer flooding application. The incremental oil recovery directly associated with polymer flooding, which includes both the polymer flooding and post‐polymer waterflooding stages (excluding the initial waterflooding injection (or secondary) oil recovery), demonstrates that the designed terpolymers provided a higher incremental recovery (42% and 58%) than the reference materials (33% and 46%). Therefore, the terpolymers provided a higher contribution to incremental (or enhanced) oil recovery than the typical HPAM. Additionally, both designed terpolymers showed better injectivity in unconsolidated porous media and are less likely to cause plugging than the commercially available reference materials. Therefore, using a targeted design approach ultimately led to polymeric materials with excellent performance for EOR polymer flooding applications. [ABSTRACT FROM AUTHOR]

A new terpolymer acceptor is presented, comprising various ratios of the same dithienothienopyrrolobenzothiadiazole (BTP) core with different side chains—alkoxy side chains (BTPO‐IC) and alkyl side chains (BTP‐IC)—and thiophene units, for use in all‐polymer organic photovoltaics. Devices incorporating binary blends of this terpolymer and the polymer PM6 as the active layer displayed open‐circuit voltages (VOC) that increase linearly upon increasing the molar ratio of BTPO‐IC. For example, the optimized device incorporating PM6:PY‐0.2OBO (i.e., with 20 mol% of BTPO‐IC) (1:1.2 wt.%) blend, with the smallest domain sizes but largest coherence length and combined face‐on and edge‐on orientation fractions among all blends, have a champion power conversion efficiency (PCE) of 16.7% (VOC = 0.97 V; JSC = 25.2 mA cm−2; FF = 0.68), whereas the device containing a similar blend ratio of the PM6:PY‐OD:PY‐OBO ternary blend (1:0.96:0.24 wt.%) displayed a PCE of 8.6% (VOC = 0.969 V; JSC = 18.7 mA cm−2; FF = 0.48). The device with PM6:PY‐0.2OBO displays better thermal stability than the devices with PM6: PY‐OD or PY‐OBO. Thus, employing terpolymer acceptors with differently functionalized side‐chain units can be an effective approach for simultaneously optimizing the aggregation domain and enhancing the PCEs and thermal stabilities of all‐polymer devices. [ABSTRACT FROM AUTHOR]

Creating new donor materials is crucial for further advancing organic solar cells. Random terpolymers have been adopted to overcome shortcomings of regular alternating donor–acceptor (D‐A) polymers of which the performance is often susceptible to batch‐to‐batch variations. In general, the properties and performance of efficient D1‐A‐D2‐A and D‐A1‐D‐A2 terpolymers are sensitive to the D1/D2 or A1/A2 monomer ratios. Side‐chain hybridization is a strategy to address this problem. Here, six D1‐A‐D2‐A‐type random terpolymers comprising D1 and D2 monomers with the same π‐conjugated D unit but with different side chains were synthesized. The side chains, containing either fluorine or trialkylsilyl substituents were chosen to provide near‐identical optoelectronic properties but provide a tool to create a better‐optimized film morphology when blended with a non‐fullerene acceptor. This strategy allows improving the device performance to over 18 %, higher than that obtained with the corresponding D1‐A or D2‐A bipolymers (around 17 %). Hence, side‐chain hybridization is a promising strategy to design efficient D1‐A‐D2‐A terpolymer donors that are insensitive to the D1/D2 monomer ratio, which is beneficial for the scaled‐up synthesis of high‐performance materials. [ABSTRACT FROM AUTHOR]

Planar building block B2TCl with C2V symmetry configuration is designed to prepare polymer donors (PB2TCl‐o and PB2TCl‐i) with good solubility in non‐halogenated solvents. When blended with BTP‐ec9‐4F, PB2TCl‐o‐based devices processed by 1,2‐dimethylbenzene (o‐DMB) give a power conversion efficiency (PCE) of 15.10% with a Voc of 0.89 V, a Jsc of 24.37 mA cm–2, and an fill factor of 69.69%. Semitransparent OSCs based on PB2TCl‐o:BTP‐ec9‐4 can afford a PCE of 9.09% with an average visible transmittance (AVT) of 23.9% and an AT of 24.2%. B2TCl‐o is also used as a third component to prepare random terpolymers PW1 and PW2. Using o‐DMB as the processing solvent, PW1 and PW2‐based devices give improved PCEs of 16.26% and 17.19%, respectively, which are much higher than the parent polymers (PM6 and D18). This work provides a versatile building block B2TCl‐o for the preparation of non‐halogen solvent processable high‐performance polymer donor materials. [ABSTRACT FROM AUTHOR]

Although breakthroughs have been made in organic solar cells (OSCs) in recent years, the power conversion efficiency (PCE) of OSCs still lags behind inorganic/perovskite solar cells. In this work, two terpolymers were synthesized by introducing the thieno[3,4‐c]pyrrole‐4,6‐(5H)‐dione (TPD) block into the host polymer donor PM6. Owing to the lower highest occupied molecular orbital energy level, wider light absorption, optimal molecular packing, and more desirable aggregation morphology by addition of the TPD, the PM6‐TPD‐5 % : Y6‐based device displayed an improved PCE of 16.3 % with an enhanced open‐circuit voltage (VOC) of 0.860 V, relative to that of PM6‐TPD‐10 % : Y6 (PCE=14.8 %) and PM6 : Y6‐based device (PCE=15.6 %). Interestingly, the VOC did not always increase in proportion to the third component. Besides, ternary OSCs based on PM6 : PM6‐TPD‐5 % : Y6 achieved a superior PCE of 17.1 %. This work demonstrated that random copolymerization is a feasible and effective strategy to further increase device performance, and the two polymers that possess similar structure and absorption in ternary devices can also obtain impressive efficiency. [ABSTRACT FROM AUTHOR]

Recently, a random ternary copolymerization strategy has become a promising and efficient approach to develop high‐performance polymer donors for polymer solar cells (PSCs). In this study, a low‐cost electron‐withdrawing unit, 2,5‐bis(4‐(2‐ethylhexyl)thiophen‐2‐yl)pyrazine (PZ‐T), is incorporated into the polymer backbone of PM6 as the third component, and three D‐A1‐D‐A2 type terpolymers PMZ‐10, PMZ‐20, and PMZ‐30 are synthesized by the random copolymerization strategy, with the PZ‐T proportion of 10%, 20%, and 30%, respectively. The terpolymers exhibit downshifted highest occupied molecular orbital energy levels than PM6, which is beneficial for obtaining higher open‐circuit voltage (Voc) of the PSCs with the polymer as a donor. Importantly, the PSCs based on PMZ‐10:Y6 demonstrate efficient exciton dissociation, higher and balanced electron/hole mobilities, desirable aggregation, and high power conversion efficiency of 18.23%, which is the highest efficiency among the terpolymer‐based PSCs so far. The results indicate that the ternary copolymerization strategy with PZ‐T as the second A‐unit is an efficient approach to further improve the photovoltaic performance and reduce the synthetic cost of the D‐A copolymer donors. [ABSTRACT FROM AUTHOR]

Semitransparent organic solar cells (ST‐OSCs) based on all narrow bandgap (all‐NBG) semiconductors are attractive for building integration. Unfortunately, advanced NBG Y‐series acceptors cannot well match with the NBG donors, resulting from their mismatched energy levels and poor compatibility. Herein, a facile terpolymer design strategy is adopted to improve the matching of Y6 with efficient NBG polymer donor PCE10. F or Cl atom functionalized benzodithiophene (BDT) are introduced into the PCE10 matrix to afford two series of terpolymers, namely PCE10‐BDT2F and PCE10‐BDT2Cl. Compared with PCE10, all terpolymers show deeper energy levels, higher extinction coefficients, enhanced face‐on orientation, and better compatibility with Y6. Consequently, significant breakthroughs are achieved for both opaque and semitransparent devices. Particularly, a record power conversion efficiency (PCE) of 13.80% is achieved by PCE10‐BDT2F:Y6‐based device, nearly 40% higher than PCE10:Y6‐based device. ST‐OSCs also achieve impressive PCEs of 12.00% and 10.85% with average visible transmittance (AVT) of 30.98% and 41.08%, respectively, and both PCEs are the highest values with AVT over 30% and 40%. An outstanding light utilization efficiency (LUE) of 4.46% further demonstrates the successful balance of PCE and AVT. These results demonstrate that the design of NBG terpolymers is a facile and highly encouraging strategy for promoting breakthroughs in ST‐OSCs. [ABSTRACT FROM AUTHOR]

Donor–acceptor (D–A) copolymer‐based polymer solar cells (PSCs) processed with nonhalogenated solvents exhibit relatively low power conversion efficiencies (PCE) due to undesirable morphological properties, including high aggregation and unfavorable orientation. Moreover, they show very poor long‐term stability owing to excessive molecular aggregation and unfavorable phase separation. Thus, novel p‐type polymers are required for high‐efficiency and long‐lived PSCs that can be processed in ecofriendly nonhalogenated solvents. Herein, a novel series of 1D/2A terpolymers (PBTPBD) composed of 4,8‐bis(5‐(2‐ethylhexyl)‐4‐fluorothiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene (BDT‐F), 1,3‐bis(thiophen‐2‐yl)‐5,7‐bis(2‐ethylhexyl)benzo‐[1,2‐c:4,5‐c′]dithiophene‐4,8‐dione (BDD), and 1,3‐bis‐(4‐hexylthiophen‐2‐yl)‐5‐octyl‐4H‐thieno[3,4‐c]pyrrole‐4,6(5H)‐dione (HT‐TPD) is synthesized and characterized for high‐efficiency and long‐lived PSCs. A PBTPBD‐50:IT‐4F blended film exhibits a favorable face‐on orientation and superior hole and electron mobility. Therefore, the corresponding PBTPBD‐50:IT‐4F PSC, processed with a nonhalogenated solvent, exhibits a high PCE of 13.64%, which is 13% higher than that of the related nonhalogenated solvent‐processed PSCs. Furthermore, the PBTPBD‐50:IT‐4F PSC maintains 82% of the initial PCE even after 204 days at 85 °C, which is the highest thermal stability achieved among PSCs processed with nonhalogenated solvents. The high‐efficiency and superior long‐term thermal stability of the PBTPBD‐50:IT‐4F PSC are attributed to the excellent miscibility of PBTPBD‐50 and IT‐4F and the suppression of the morphological changes in the photoactive layer. [ABSTRACT FROM AUTHOR]

Regulating molecular structure to optimize the active layer morphology is of considerable significance for improving the power conversion efficiencies (PCEs) in organic solar cells (OSCs). Herein, we demonstrated a simple ternary copolymerization approach to develop a terpolymer donor PM6‐Tz20 by incorporating the 5,5′‐dithienyl‐2,2′‐bithiazole (DTBTz, 20 mol%) unit into the backbone of PM6 (PM6‐Tz00). This method can effectively tailor the molecular orientation and aggregation of the polymer, and then optimize the active layer morphology and the corresponding physical processes of devices, ultimately boosting FF and then PCE. Hence, the PM6‐Tz20: Y6‐based OSCs achieved a PCE of up to 17.1% with a significantly enhanced FF of 0.77. Using Ag (220 nm) instead of Al (100 nm) as cathode, the champion PCE was further improved to 17.6%. This work provides a simple and effective molecular design strategy to optimize the active layer morphology of OSCs for improving photovoltaic performance. [ABSTRACT FROM AUTHOR]

Diphenylethylene (DPE) is a monomer which has attracted significant interest from academia and industry both in terms of copolymerization kinetics and for the potential to extend and tune the range of glass transition temperatures accessible for DPE‐containing copolymers. DPE can undergo (co)polymerization with a variety of other monomers by living anionic polymerization but is incapable of forming a homopolymer due to steric hindrance. DPE, being a sterically bulky monomer, results in dramatic increases in the glass transition temperature (Tg) of resulting copolymers, with a perfectly alternating copolymer of styrene and DPE having a Tg of ~180 °C. Herein we report for the first time, the outcome of the statistical terpolymerization of butadiene, styrene, and DPE—a one‐pot, one‐shot, commercially scalable reaction using monomers of wide industrial importance. This extremely facile approach produces copolymers with a block‐like structure, which undergo microphase separation, possess a high Tg glassy "block" and are virtually indistinguishable from analogous block terpolymers made by the traditional sequential addition of monomers approach. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 382–394 This study reports for the first time the outcome of the statistical terpolymerization of butadiene, styrene, and DPE—a one‐pot, one‐shot, commercially scalable reaction using monomers of wide industrial importance. This extremely facile approach produces copolymers with a block‐like structure, which undergo microphase separation, possess a high Tg glassy "block," and are virtually indistinguishable from analogous block terpolymers made by the traditional sequential addition of monomers approach. [ABSTRACT FROM AUTHOR]

A series of L‐lactide (LLA), 1,3‐trimethylene carbonate (TMC) and glycolide (GA) terpolymers (LTG) of different monomer molar ratios were synthesized by using ring‐opening copolymerization. An effective and low‐toxic zirconium (IV) acetylacetonate Zr(Acac)4 was used as catalyst. The viscosity‐average molecular weights (Mη) of obtained polymers were all above 2.2×104 g/mol. The chemical structure and viscosity of terpolymers were confirmed by Fourier transform infrared spectroscopy (FTIR), 1H nuclear magnetic resonance (1HNMR), 13C nuclear magnetic resonance (13CNMR) and an Ubbelohde viscometer. The thermal and mechanical properties were investigated by means of differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X‐ray diffraction (XRD) and stress‐strain measurements. Results suggested that all terpolymers were amorphous and showed good thermal stability. Also it was found that elongation increased with the decreasing of LLA unit. More importantly, terpolymers displayed shape memory property when deformation temperatures were 14‐15 °C above Tg. [ABSTRACT FROM AUTHOR]

Two donor-acceptor (D-A) type conjugated copolymers, P1 and P2, are designed and synthesized. A classical benzothiadiazole acceptor is used to replace a thiophene unit in the polymer chain of P1 to obtain P2 terpolymer. Compared with P1, P2 exhibits broader absorption spectra, higher absorption coefficient, deeper lowest unoccupied molecular orbital level, and a relatively lower band gap. As a result, the P2-based solar cell exhibits a high power conversion efficiency (PCE) of 6.60%, with a short-circuit current (Jsc) of 12.43 mA cm-2, and a fill factor (FF) of 73.1%, which are higher than those of the P1-based device with a PCE of 4.70%, aJsc of 9.43 mA cm-2, and an FF of 61.6%. [ABSTRACT FROM AUTHOR]

ABSTRACT Synthesis and properties of a series of ammonium-containing terpolymers (QPAF-3) as anion conductive membranes are reported. The QPAF-3s composed of perfluoroalkylene, alkylene, and ammonium-functionalized phenylene groups without heteroatom linkages in the main chain were synthesized via nickel-mediated polycondensation reaction, followed by chloromethylation, quaternization, and ion exchange reactions. Self-standing, bendable membranes were obtained by solution casting. The QPAF-3 membrane with optimized terpolymer composition and ion exchange capacity (1.46 meq g−1) showed high hydroxide ion conductivity (123 mS cm−1 in water at 80 °C). The alkaline stability test in 1 M KOH for 1000 h at 80 °C and the post-test analysis with IR spectra and tensile strength suggested that ammonium groups were likely to be decomposed while the polymer main chain was chemically more robust. The presence of the alkylene groups in the terpolymers lowered solubility, glass transition temperature, and elongation property of the resulting membranes. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 1442-1450 [ABSTRACT FROM AUTHOR]

Morphology control is one of the key strategies in optimizing the performance of organic photovoltaic materials, particularly for diketopyrrolopyrrole (DPP)-based donor polymers. The design of DPP-based polymers that provide high power conversion efficiency (PCE) presents a significant challenge that requires optimization of both energetics and morphology. Herein, a series of high performance, small band gap DPP-based terpolymers are designed via two-step side chain engineering, namely introducing alternating short and long alkyls for reducing the domain spacing and inserting alkylthio for modulating the energy levels. The new DPP-based terpolymers are compared to delineate how the side chain impacts the mesoscale morphology. By employing the alkylthio-substituted terpolymer PBDPP-TS, the new polymer solar cell (PSC) device realizes a good balance of a high Voc of 0.77 V and a high Jsc over 15 mA cm−2, and thus realizes desirable PCE in excess of 8% and 9.5% in single junction and tandem PSC devices, respectively. The study indicates better control of domain purity will greatly improve performance of single junction DPP-based PSCs toward 10% efficiency. More significantly, the utility of this stepwise side chain engineering can be readily expanded to other classes of well-defined copolymers and triggers efficiency breakthroughs in novel terpolymers for photovoltaic and related electronic applications. [ABSTRACT FROM AUTHOR]

The general concept for nitroxide-mediated radical terpolymerization is advanced. This concept is based on activation-deactivation equilibria for terminal polymer-nitroxide adducts. Depending on monomer activity and the stability of terminal nitroxide adducts, terpolymerization can be equilibrium living, quasi-equilibrium (gradient) living, decaying living, decaying gradient, or non-living. Expressions for the effective activation-deactivation equilibrium constant, Kef, and the rate of terpolymerization are derived from theoretical speculations on equilibrium living and decaying living terpolymerization. For quasi-equilibrium living terpolymerization, various types of gradient terpolymers are predicted. When activity of the active monomer M1 is, at least, one order of magnitude different from that of the two other monomers, the effective constant Kef is shown to approach K1 of the most active monomer. Experimental kinetic and equilibrium constants agree with the advanced concept for the equilibrium living terpolymerization of styrene with methyl methacrylate, and acrylonitrile in the presence of nitroxide SG1, as well as for decaying living terpolymerization in the same system in the presence of nitroxide TEMPO. [ABSTRACT FROM AUTHOR]

A novel terpolymer involving 2-amino-6-nitrobenzothiazole and ethylenediamine with formaldehyde was synthesized by a polycondensation technique using glacial acetic acid as a reaction medium. The resulting chelating terpolymer resin was characterized using elemental analysis, physicochemical parameters, and UV-visible, Fourier transform infrared, 1H NMR and 13C NMR spectral studies. Average molecular weights of the terpolymer were determined using gel permeation chromatography. The surface morphology and the nature of the terpolymer were investigated using scanning electron microscopy and X-ray diffraction. The chelation ion-exchange property of the terpolymer was determined against some common metal ions such as Fe3+, Co2+, Ni2+, Cu2+, Zn2+ and Pb2+ using the batch equilibrium method. Effects of parameters such as the pH, contact time and various electrolyte concentrations were studied. The reusability of the terpolymer was checked in terms of its effective repeated usage. The results of the Langmuir and Freundlich adsorption isotherm models were best fitted with each other and the reaction kinetics followed pseudo second-order kinetics. The terpolymer showed good results against Fe3+, Cu2+ and Ni2+ ions compared to those against the other metal ions. © 2014 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

An N-vinylimidazole-based monomer carrying an adamantyl group, (1-vinyl-2-yl)methyl­adamantan-1-ylcarbamate ( 3), is synthesized. The terpolymerization with N-vinylimidazole ( 4) and 1-vinyl-2-(hydroxymethyl)imidazole ( 2) yields terpolymers ( 5a-b) with high upper critical solution temperature (UCST)-type transitions in water. The solubility can be influenced by the addition of various amounts of randomly methylated β-cyclodextrin (RAMEB-CD). It is found that supramolecular host/guest interaction clearly controls the solution behavior. [ABSTRACT FROM AUTHOR]

Copolymerization of norbornene and 7-octenyldiisobutylaluminium is conducted by the catalytic system of ansa-dimethylsilylene(fluorenyl)(amido)dimethyltitanium, Me2Si(N tBu)(fluorenyl)TiMe2 ( 1), activated with Ph3CB(C6F5)4 to produce copolymers with pendant alkylaluminium groups. The termination of the copolymers with methanol gives poly(norbornene- co-oct-1-ene). Termination with oxygen gas gives poly(norbornene- co-oct-1-ene- co-oct-7-en-1-ol) because the oxidation of the pendant alkylaluminium groups with oxygen is not quantitative. Terpolymerization of norbornene, oct-1-ene, and 7-octenyldiisobutylaluminium are also conducted, where the content of the hydroxy groups and the glass transition temperature are independently controlled by the molar ratio of each comonomer in feed. [ABSTRACT FROM AUTHOR]

ABSTRACT Terpolymers based on propylene with 1-pentene and 1-hexene as comonomeric units are satisfactorily synthesized using a metallocene catalyst. Thus, several terpolymers are prepared with distinct overall compositions in comonomers as well as three different 1-pentene/1-hexene ratios at a given composition to evaluate the influence on polymerization activity, intrinsic viscosity, and microstructural details. The new trigonal δ polymorph is observed in those quenched terpolymers with a global content in comonomers of about 14 mol %, independently of the ratio between both comonomers. However, preliminary results indicate a profound influence of that ratio on the crystallization rate. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3251-3259 [ABSTRACT FROM AUTHOR]

Carbazoles constitute one of the most widely used donor moieties for organic semiconductors due to their excellent hole transport and high environmental stability. However, they are seldomly used in recent high performance donor–acceptor (D–A) copolymers. In the present study, a planar regular terpolymer, PCbisDPP, composed of carbazole and thiophene flanked bis‐diketopyrrolopyrrole (bis‐DPP) for application as an active layer for high‐performance organic devices is reported. Organic field‐effect transistors with PCbisDPP as the active layer exhibit field‐effect mobility up to 1.48 cm2 v−1 s−1, which to the best of the current knowledge corresponds to the highest hole mobility reported to date for carbazole‐based D–A polymers. The high mobility is achieved via a tailored polymer‐design resulting in high crystallinity and a strong aggregating property without sacrificing solubility. PCbisDPP is applied as an active donor material in organic photodiode with fullerene derivative PC61BM as an acceptor in a bulk heterojunction blend. Binary additive combinations (tetralin: 1,8‐diiodooxtane (3:3) v/v%) utilization achieves an impressive performance with an external quantum efficiency of 80%, an average responsivity of 309.1 mA W−1, and specific detectivity of 4.73 × 1011 Jones in the near infra‐red light region (730 nm) utilizing a simple single layer organic photodiode structure as ITO/PEDOT:PSS/PCbisDPP:PC61BM/LiF/Al. [ABSTRACT FROM AUTHOR]

White Organic Light‐Emitting Diodes (WOLEDs) have attracted an enormous interest because they can be implemented in numerous lighting applications as next‐generation light sources. Several device setups such as multilayer, blends, or single layers of polymer nanomaterials have been proposed to achieve white light emission. In this work, novel copolymers bearing blue, yellow, and red chromophores, are used for the fabrication of WOLED systems including single emissive layer. These terpolymers provide easy tuning of white color emission by selecting the appropriate ratios between the chromophores while being solution processable from typical organic solvents, like chlorobenzene (CB), o‐dichlorobenzene (o‐DCB), etc. The chromophores can be directly excited by capturing charge carriers or through energy transfer from the other chromophores. Incomplete energy transfer between the chromophores is necessary to get white light as combined emission from all of them. The opto‐electronic and electro‐optical characterization is carried out by NIR–Vis–far UV spectroscopic ellipsometry, photoluminescence, and electroluminescence, to provide valuable information toward the optimization and functionalization of these WOLED devices. Novel copolymers bearing blue, yellow, and red chromophores, are used for the fabrication of white organic light‐emitting diode (WOLED) systems including single emissive layer. These terpolymers provide easy tuning of white colour emission by selecting the appropriate ratios between the chromophores while being solution processable. The opto‐electronic and electro‐optical characterization is carried out by NIR–Vis–far UV spectroscopic ellipsometry, photoluminescence, and electroluminescence. [ABSTRACT FROM AUTHOR]