Host Blend Research Articles

PVA/CMC/PEG blended polymer loaded with ZnCo1.9Al0.1O4/carbon nanoparticles/PANi as a promising films for UV radiation shielding

Polyvinyl alcohol (PVA), carboxymethyl cellulose (CMC) and polyethylene glycol (PEG) have been employed as polymeric matrices for the synthesis of polymeric nanocomposite films that incorporate ZnCo1.9Al0.1O4, carbon nanoparticles (CNPs) and polyaniline (PANI) as fillers. X-ray diffraction technique was utilized to examine the structure of ZnCo1.9Al0.1O4 filler and the formed PVA/CMC/PEG/ZnCo1.9Al0.1O4/CNPs/x wt % PANi blends. The morphology of the doped blend was explored using the scanning electron microscopy technique. The increases in absorbance, especially in the UV spectrum, demonstrate the potential of these blends in UV-blocking and UV-filtering applications. The minimum direct and direct optical energy gaps are 5.62 and 4.77 eV obtained as the quantity of PANi became 0.3 wt %. The highest refractive index values (n = 1.66 at 600 nm) were acquired as the blend was doped with 0.4 wt % PANi. The impact of different fillers on the linear and nonlinear optical parameters was explored. The inclusion of ZnCo1.9Al0.1O4/CNPs/x wt % PANi resulted in an improvement in PVA/CMC/PEG blended polymer's optical conductivity. The FL intensities of the loaded blends are comparatively lower than those of the undoped blend. The values of the dielectric constants of doped blends with x = 0 or 0.4 are notably higher than those of other blends. Doped blend with x = 0.2 exhibited the highest energy density value (9 × 10−3 J/m3 at 1 kHz). The doped blend with x = 0.4 has the highest ac conductivity (1.53 × 10−8 Sm−1 at 1 kHz). The influence of doping on the relaxation time and capacitance behavior of the host blend was inspected. These outcomes suggest the opportunity of employing the created nanocomposites in capacitive energy storage and optoelectronic devices.

Polyvinyl alcohol/carboxymethyl cellulose blended polymers doped with PPy/milled MWCNTs filler for Flexible optoelectronic and Energy Storage Applications

Using the solution casting procedure, poly (vinyl alcohol)/carboxymethyl cellulose/polypyrene/milled multiwall carbon nanotubes, PVA/CMC/PPy/x wt% milled MWCNTs blended polymers were formed. X-ray diffraction and scanning electron microscopy were employed to inspect the structure and morphology of the resulted blends. The lowest direct and indirect optical band gaps are (5, 4.3) eV and (4.37, 3.38) eV, respectively, achieved when the MWCNTs content in the doped blend was 0.25 wt %. By incorporating varying quantities of milled MWCNTs into the PVA/CMC/PPy blended polymer, consistent enhancements were observed in the optical dielectric constant and optical conductivity values. The blend with 0.25 wt% MWCNTs exhibited the maximum values of refractive index. The maximum electric dielectric constant and energy density values were attained as x = 0.15. The temperature impacted the dielectric constants and energy storage values. All blends fit with the CBH model. The impact of MWCNTs doping level and the temperature on the impedance spectroscopy and electric modulus of the host blend was explored. The sample with x = 0.15 has the smallest relaxation time. The impact of MWCNTs doping level on the dc conductivity, activation energy and conductivity mechanism of the host blend was explored. The doped blends with x = 0.15 is viable materials for energy storage purposes.

Exploring the optical and electric features of PMMA/PVAc blended polymers doped with TBAI/MWCNTs fillers for different applications

The present study focuses on the production of poly (methyl methacrylate)/poly (vinyl acetate)/tetrabutylammonium iodide/multi-walled carbon nanotubes (PMMA/PVAc/TBAI/x wt %MWCNTs) blended polymers. These blends show great potential for use in advanced optical, energy storage and electronics applications. X-ray diffraction (XRD) and scanning electron microscopy techniques was used to explore the structure and morphology of PMMA/PVAc/TBAI with x wt% MWCNTs blended polymers. The optical transmittance lowered to a minimum value of 53–63 % within the specific wavelength range as the blend contained 0.55 wt % multi-walled carbon nanotubes (MWCNTs). The sample containing 0.11 wt% MWCNTs demonstrated the highest reflectance (R) values, whereas the sample with 0.55 wt% MWCNTs showed the lowest R values. As the concentration of MWCNTs increased, these values consistently decreased. The smallest direct (4.55 eV) and indirect (4.45 eV and 2.48 eV) optical band gap (Eg) values were achieved when wt% of MWCNTs were 0.44 % and 0.55 %, respectively. The doped blend with wt% of 0.11 exhibited the highest refractive index values. Blend with x = 0.55 wt % MWCNTs has the highest dielectric constant. The energy density (U) increased non-uniformly as the blend was infused with MWCNTs. Elevating the temperature enhances the values of U for all blends. All blends adhered to the correlated barrier hopping (CBH) model. The effects of MWCNTs doping amount and temperature on the impedance and electric modulus of the host blend were investigated. The dc conductivity of the doped samples was observed to be greater than that of the undoped blend, except for the blend with x = 0.44, where it diminished. The undoped blend displayed activation energy (Ea) values of 1.71 eV and 0.6 eV, depending on the temperature range. When the host blend is doped with MWCNTs, the Ea values either rise or fall depending on the quantity of MWCNTs. All samples have non-ohmic characteristics.

Structural, optical and electrical conduction characteristics of PMMA/PVAc/TBAI blended polymers

This study aims to create tetra-n-butylammonium iodide (TBAI) doped poly(methyl methacrylate) (PMMA)/polyvinyl acetate (PVAc) blended polymers for utilize in a diversity of optoelectronic applications. By the casting technique, the films of (PMMA/PVAc/x wt % TBAI) were formed. The structure and morphology characteristics of the blended materials were studied using X-ray diffraction and scanning electron microscopy techniques. The optical transmittance declined to a minimum value when the blend was loaded with 38 wt % TBAI. The blend containing 38 % TBAI exhibits the highest reflectance values in the visible range. The lowest direct optical bandgap energies (4.20 eV) and indirect optical bandgap energies (3.71 eV, 3.13 eV) were achieved when TBAI reached 38 wt%. The addition of TBAI leads to an enhancement of the refractive index values of PMMA/PVAc in the visible spectrum. The effect of TBAI doping amount on the optical dielectric constant, energy loss functions, optical conductivity, nonlinear optical parameters and emitted color of the host blend was explored. The maximum values of the optical dielectric constant and energy loss functions were achieved after the TBAI level reached 38 wt%. The three non-linear optical (NLO) parameters for PMMA/PVAc blended polymers were enhanced as the amount of TBAI increased. An increase in voltage (V) or temperature results in a significant increase in electric current (I). Raising the amount of TBAI doping also caused the electric current to rise irregularly, with the exception of the blend with x = 11 %, where it fell. The samples exhibited the non-ohmic characteristics of the current-voltage (I–V) properties. The conduction mechanism of all blended materials was studied in detail. Finally, the outcomes supported the optical and electric properties studies, which suggested that a range of nanoelectronics applications could make use of the PMMA/PVAc/x weight percent TBAI blended polymers.

PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers: Improved the physical properties for energy storage devices and optoelectronic applications

The current investigation aims to enhance the optical and dielectric properties of poly (vinyl alcohol) (PVA)/polyethylene glycol (PEG) blended polymers via loading with copper cobaltite (CuCo2O4), polyaniline (PANi), and x wt% multi-walled carbon nanotubes (MWCNTs) for potential applications in optoelectronics and capacitive storage. The fabrication of PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers was carried out via casting and hydrothermal methods. Characterization of the blended polymer's structure and morphology was conducted using X-ray diffraction and scanning electron microscopy techniques. The impact of various fillers on the linear and nonlinear optical properties of the host blend was analyzed. The loaded blends demonstrated efficacy in blocking UVA, UVB, and UVC spectra, making them suitable absorbers for solar cells. The lowest values for direct and indirect optical band gap energy (Eg), of 5.34 eV and 4.44 eV were attained at x = 0.02. The blend with x = 0.01 displays the highest refractive index at λ = 600 nm. The optical conductivity exhibited nonmonotonically growth until peaking at x = 0.01. Analysis of chromaticity diagrams in CIE 1931 color space reveals that all blends emit blue-violet hues with slight variations in intensity. The fluorescence (FL) intensity of the doped blend is notably lower compared to the undoped counterparts. The doped blend (x = 0.03) showcases superior dielectric constants and ac conductivity values. The maximum energy density was achieved at 1 kHz for the host blend incorporating CuCo2O4/PANi. Overall, the observed characteristics indicate that PVA/PEG/CuCo2O4/PANi/x wt% MWCNTs blended polymers represent promising hybrid nanomaterials suitable for diverse applications.

Exploiting Mechanism of Enhanced Charge Transfer in Ternary Organic Solar Cells at Low Energy Loss

The structural disorder and aggregation of the third acceptor with the host active layer are critical in the light absorption, film morphology, and charge‐carrier mechanism of their photovoltaic blends to achieve highly efficient organic solar cells (OSCs). However, an effective third component needs to be introduced in the host binary blend as a combination of ternary blend, which can improve the absorption profile, film morphology, and charge dynamics. In this work, non‐fullerene acceptor DRCTF is incorporated as a third component in host PM6:Y6 binary blend. Compared to host blend, the ternary blend improves charge‐transfer processes, as evidenced by steady‐state photoluminescence and time‐resolved photoluminescence measurements. It is found that the addition of 20% DRCTF into host binary blend results in improved charge dissociation and transport with reduced recombination, and voltage losses. All these characteristics contribute to an improved power conversion efficiency of 14.45% in the PM6:Y6:DRCTF ternary OSCs (T‐OSCs), compared to PM6:Y6 (12.46%) in open‐air fabrication conditions. Consequently, in this study, the impact of third components on the charge‐transfer mechanism in T‐OSCs is elucidated. These findings suggested that T‐OSCs with a perfectly chosen third component in the host binary blend achieve a comprehensive absorption profile, smooth film morphology, efficient charge dynamics, and reduced voltage loss.

Modification in the Optical and Dielectric Characteristics of Poly (Vinyl Alcohol)/Carboxymethyl Cellulose Blended Polymers Doped with Two Phases Nanocomposites for Application in Optoelectronic and Energy Storage Devices

Nanocomposite films comprised of poly (vinyl alcohol) (PVA) and carboxymethylcellulose (CMC) were fabricated via a solution casting procedure, with the incorporation of (1-x)CuCo2O4/xZnMn2O4. Our research described here was aimed to explore the impact of the (1-x)CuCo2O4/xZnMn2O4 on the structural, optical and electrical features of the PVA/CMC blended polymer, using various techniques. The different phases formed (CuCo2 O4 and/or ZnMn2O4) in (1-x) CuCo2O4/x ZnMn2O4 filler samples were identified applying Rietveld refinement analysis. The structures and morphologies of the PVA/CMC/(1-x)CuCo2O4/xZnMn2O4 blend composites were determined using X-ray diffraction and scanning electron microscopy techniques. Their various linear and nonlinear optical parameters were examined using the diffused reflectance technique. The blended polymer composite with x = 0.1 displayed the highest absorbance. The transmittance of the PVA/CMC blend declined from 91 to 69% when it was loaded with a nanocomposite containing 10% ZnMn2O4. The optical band gaps of the doped blend composites had their lowest values, 5.45 eV for direct transition and (4.83, 2.99, 2.31) eV for the indirect transition, as the blend was loaded with the fillers containing 10 and 15% ZnMn2O4. The study also explored the influence of the (1-x)CuCo2O4/x ZnMn2O4 on the fluorescence spectra and chromaticity diagram of the PVA/CMC blend. The effect of the filler on the complex dielectric constant, complex electric modulus, ac conductivity and electrical storage energy of the host blend was examined. The obtained characteristics imply potential utility of the doped blends in photocatalytic, UV-blocking, UV-filtering, optoelectronic, electrical storage, nonlinear optical and photonic applications.

Non-halogenated Solvent-Processed Organic Solar Cells with Approaching 20 % Efficiency and Improved Photostability.

The development of high-efficiency organic solar cells (OSCs) processed from non-halogenated solvents is crucially important for their scale-up industry production. However, owing to the difficulty of regulating molecular aggregation, there is a huge efficiency gap between non-halogenated and halogenated solvent processed OSCs. Herein, we fabricate o-xylene processed OSCs with approaching 20 % efficiency by incorporating a trimeric guest acceptor named Tri-V into the PM6:L8-BO-X host blend. The incorporation of Tri-V effectively restricts the excessive aggregation of L8-BO-X, regulates the molecular packing and optimizes the phase-separation morphology, which leads to mitigated trap density states, reduced energy loss and suppressed charge recombination. Consequently, the PM6:L8-BO-X:Tri-V-based device achieves an efficiency of 19.82 %, representing the highest efficiency for non-halogenated solvent-processed OSCs reported to date. Noticeably, with the addition of Tri-V, the ternary device shows an improved photostability than binary PM6:L8-BO-X-based device, and maintains 80 % of the initial efficiency after continuous illumination for 1380 h. This work provides a feasible approach for fabricating high-efficiency, stable, eco-friendly OSCs, and sheds new light on the large-scale industrial production of OSCs.

Non‐halogenated Solvent‐Processed Organic Solar Cells with Approaching 20 % Efficiency and Improved Photostability

AbstractThe development of high‐efficiency organic solar cells (OSCs) processed from non‐halogenated solvents is crucially important for their scale‐up industry production. However, owing to the difficulty of regulating molecular aggregation, there is a huge efficiency gap between non‐halogenated and halogenated solvent processed OSCs. Herein, we fabricate o‐xylene processed OSCs with approaching 20 % efficiency by incorporating a trimeric guest acceptor named Tri‐V into the PM6:L8‐BO‐X host blend. The incorporation of Tri‐V effectively restricts the excessive aggregation of L8‐BO‐X, regulates the molecular packing and optimizes the phase‐separation morphology, which leads to mitigated trap density states, reduced energy loss and suppressed charge recombination. Consequently, the PM6:L8‐BO‐X:Tri‐V‐based device achieves an efficiency of 19.82 %, representing the highest efficiency for non‐halogenated solvent‐processed OSCs reported to date. Noticeably, with the addition of Tri‐V, the ternary device shows an improved photostability than binary PM6:L8‐BO‐X‐based device, and maintains 80 % of the initial efficiency after continuous illumination for 1380 h. This work provides a feasible approach for fabricating high‐efficiency, stable, eco‐friendly OSCs, and sheds new light on the large‐scale industrial production of OSCs.

Crossbreeding Effect of Chalcogenation and Iodination on Benzene Additives Enables Optimized Morphology and 19.68% Efficiency of Organic Solar Cells.

Volatile solid additives have attracted increasing attention in optimizing the morphology and improving the performance of currently dominated non-fullerene acceptor-based organic solar cells (OSCs). However, the underlying principles governing the rational design of volatile solid additives remain elusive. Herein, a series of efficient volatile solid additives are successfully developed by the crossbreeding effect of chalcogenation and iodination for optimizing the morphology and improving the photovoltaic performances of OSCs. Five benzene derivatives of 1,4-dimethoxybenzene (DOB), 1-iodo-4-methoxybenzene (OIB), 1-iodo-4-methylthiobenzene (SIB), 1,4-dimethylthiobenzene (DSB) and 1,4-diiodobenzene (DIB) are systematically studied, where the widely used DIB is used as the reference. The effect of chalcogenation and iodination on the overall property is comprehensively investigated, which indicates that the versatile functional groups provided various types of noncovalent interactions with the host materials for modulating the morphology. Among them, SIB with the combination of sulphuration and iodination enabled more appropriate interactions with the host blend, giving rise to a highly ordered molecular packing and more favorable morphology. As a result, the binary OSCs based on PM6:L8-BO and PBTz-F:L8-BO as well as the ternary OSCs based on PBTz-F:PM6:L8-BO achieved impressive high PCEs of 18.87%, 18.81% and 19.68%, respectively, which are among the highest values for OSCs.

Comparative analysis of the optical and electrical properties of PVA/PVP blended polymer with ZnCo2O4/CdS nanocomposites for optoelectronic and dielectric capacitor applications

Polymer nanocomposite blends were produced using solution casting, hydrothermal and thermolysis techniques. The blends were composed of a polymer blend consisting of polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) as the organic host matrix with (1−x)ZnCo2O4–xCdS as filler samples. The current study investigated the morphological, structural, optical, and dielectric features of PVP/PVP/(1-x)ZnCo2O4/xCdS blends. The crystallite size and the phases formed in the fillers were obtained using Rietveld method. The structure and morphology of blended samples were studied using X-ray diffraction and scanning electron microscope techniques. The results of the optical properties imply that the linear and nonlinear optical parameters were affected by the amount of CdS in the (1-x)ZnCo2O4/xCdS filler samples. The direct allowed, indirect allowed, direct forbidden and indirect forbidden transitions values were reduced to 5.09, 4.55, 4.67 and 4.12 eV, respectively, as (1-x)ZnCo2O4/xCdS with x = 0.05 was incorporated into the PVA/PVP blend. The nature of electronic transitions in all blends were also studied. The fluorescence intensity, emitted colors and purity of the doped PVA/PVP blend are affected by the amount of CdS in the fillers and the excitation wavelength. The energy density of the host blend was improved as it loaded with fillers contained 5 and 10 % CdS in the frequency range beyond 1 kHz. The relaxation times of all doped blends were diminished except blend contained 25% CdS, the relaxation time rose slightly as compared with the relaxation time of undoped blend. The obtained properties indicates potential utility of the doped blends in photocatalytic, photonic, storage energy and optoelectronic applications.

Tuning the optical, and dielectric properties of PVC/PEO/NiMoO4/MWCNTs/x wt %PANI blended polymers for optoelectronic applications

Nanoparticles of nickel molybdate (NiMoO4) have attracted significant interest for their application as electrode materials. Here, new hybrid blended polymers, poly (vinyl chloride)/polyethylene oxide/nickel molybdate/multi-walled carbon nanotubes/polyaniline (PVC/PEO/NiMoO4/MWCNTs/x wt %PANI) were prepared. Several techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), diffused reflectance, fluorescence and LCR meter were used to investigate the impact of the different fillers on the structure, electrical and optical features of the PVC/PEO blend. The structures of NiMoO4 and different blends were explored using XRD technique. The linear and nonlinear optical properties and the emitted colors of host blend are found to be affected by NiMoO4, MWCNTs and different amounts of PANI fillers. The T values of PVC/PEO were reduced as it loaded with NiMoO4/MWCNTs/x wt %PANI and it reached its minimum value (21–37% in the visible range) in NiMoO4/MWCNTs/x 0.4 %PANI blend. The minimum direct and indirect optical band gap values (4.09, 4.9) eV and (1.92, 3.47, 3.94) eV, respectively, were obtained as the amount of PANI became 0.4 wt % in the doped blend. The doped PVC/PEO blend with NiMoO4 has the highest refractive index value (2.11) at 600 nm. The highest nonlinear optical parameters were acquired exclusively in the visible spectrum when PVC/PEO was doped with NiMoO4.The maximum energy density value (6.03 × 10−3 J/m3) was obtained when the host blend loaded with NiMoO4/MWCNTs. Thus, PVC/PEO/NiMoO4/MWCNTs/x wt %PANI blends are recognized as a good prospect for UV blocking, solar cell, optoelectronic, nonlinear optical devices and energy storage innovation.

Optical and Dielectric Characteristics of Poly (Methyl Methacrylate)/Polyethylene Oxide/Carbon Nanoparticle Composites Loaded with Nano NiFe2O4

The current study proposes a simple, low-cost, and functional method of doping a pure matrix of poly (methyl methacrylate)/polyethylene oxide/carbon nanoparticles (PMMA/PEO/CNPs) with nano nickel ferrite (NiFe2O4) as a filler. To create NiFe2O4 nanoparticles, a straightforward chemical growth, sol-gel auto-combustion system was used. Next, environmentally friendly and cost-effective, undoped and blended polymers doped with NiFe2O4 using a solution-casting method were synthesized. Rietveld refinement analysis was used to investigate the structure and microstructure of the NiFe2O4. Transmittance electron microscopy was used to confirm the nano nature of the filler. X-ray diffraction was used to verify the crystallite nature of the undoped and doped PMMA/PEO/CNPs blends with NiFe2O4. The linear optical characteristics of the proposed blends were obtained using a diffuse reflectance spectrophotometer. The measured optical parameters included transmittance, absorbance, reflectance, direct and indirect optical bandgaps, absorption coefficient, linear refractive index, extinction coefficient, dielectric constant, energy loss functions, in addition to optical and electrical conductivities. Also, nonlinear optical constants for the synthesized blends, such as the linear and third nonlinear susceptibilities, nonlinear refraction coefficient and nonlinear absorption coefficient, were calculated. The direct and indirect optical band gap energies of the PMMA/PEO/CNPs blends were 4.97 and 4.8 eV, respectively. As the NiFe2O4 doping level increased in the blend to 2.5 wt%, the optical band gap energy values decreased to 4.54 and 4.64 eV, respectively. The fluorescence spectra of the undoped and doped PMMA/PEO/CNPs blended polymers with nano NiFe2O4 were also explored. The effect of NiFe2O4 doping amount on the energy density, electric dielectric constant, ac conductivity and electric moduli of the host blend was also studied. In conclusion, the considered NiFe2O4-doped PMMA/PEO/CNPs blends have an effective and promising role in optoelectronic applications.

Impact of ZnMn2O4/CdS nanocomposite on the structural, optical and dielectric characteristics of PMMA/PEO blend

Herein, polymethyl methacrylate (PMMA)/ polyethylene oxide (PEO) blend doped with nanocomposite (1 − x) ZnMn2O4/xCdS samples were prepared through two steps, the first comprising nanocomposite (1 − x) ZnMn2O4/xCdS samples synthesizing, while the second was the incorporation of nanocomposites into the blend matrix, and finally the films were obtained through the casting solution method. Various techniques, such as X-ray diffraction, scanning electron microscopy, diffused reflection and impedance spectroscopy were used to determine the change in the PMMA/PEO structure after the inclusion of the nanocomposites. The direct and indirect optical bandgap values for the PMMA/PEO blend decreased from 5.04 and 4.8 eV to 4.99 and 4.7 eV, respectively, as the blend doped with (1 − x) ZnMn2O4/xCdS samples. At 600 nm, the refractive index of the blend was raised from 1.37 to 1.53 as it doped with 0.9 ZnMn2O4/0.1CdS sample. The linear and nonlinear optical parameters grow with the insertion of (1-x)ZnMn2O4/xCdS nanocomposites into the PMMA/PEO blend. Variation of CdS in the doped nanocomposites affects slightly the linear and nonlinear optical parameters of the host blend. Blend containing 10 % CdS has the highest linear and nonlinear optical parameters as compared with other doped blends. All of the blends exhibited different shades of blue color, except for the blend that contained 10 % CdS, which displayed a violet color. The effect of doping on the dielectric properties of different blends was also explored. Blend with 20 % CdS has the highest energy density. This improvement implies the use of prepared blends in different optoelectronic, photocatalytic and storage device applications.

Preparation and tuning the optical and electrical properties of polyethylene oxide/polyvinyl alcohol/poly(3,4-thylenedioxythiophene): polystyrene sulfonate/CuO-based quaternary nanocomposites for futuristic energy storage devices

Polymeric nanocomposites have important industrial and scientific applications because they are flexible, multifunctional, and highly intelligent. Using the solution-casting technique, copper oxide nanoparticles (CuO NPs) of different concentrations (0.4, 0.8, 1.2, and 1.6 wt% to the host blend weight) were added to polymer nanocomposite films made of polyethylene oxide, polyvinyl alcohol, and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEO/PVA/PEDOT: PSS) blend. According to TEM and XRD studies, the CuO NPs of a size range of 20 to 60 nm were extremely pure and had a monoclinic structure. The PEO/PVA/PEDOT: PSS blend's semicrystalline character was reduced by the additional CuO NPs through interactions between the functional groups of blend and nanofiller, according to XRD and FTIR measurements. By adding more CuO NPs, the samples' optical bandgap energies, and UV/visible absorption spectra showed considerable changes. The electrical conductivity, impedance, and dielectric features of the samples were assessed at various frequencies, from 10−1 to 107 Hz. AC conductivity, dielectric permittivity, and dielectric loss all steadily improved as CuO NPs content rose and low permittivity at the high frequencies depicted the favourable nanodielectric features of these hybrid films. The equivalent electrical circuit using the impedance components Z′ and Z″ was introduced. The controllable optical energy gaps, frequency-dependent AC conductivity, and a large extent of composition tuneable permittivity implied the utility of PEO/PVA/PEDOT: PSS/CuO nanocomposites in developing flexible optoelectronic and energy storage devices.

18.6% Efficiency All-Polymer Solar Cells Enabled by a Wide Bandgap Polymer Donor Based on Benzo[1,2-d:4,5-d']bisthiazole.

The limited selection of wide bandgap polymer donors for all-polymer solar cells (all-PSCs) is a bottleneck problem restricting their further development and remains poorly studied. Herein, a new wide bandgap polymer, namely PBBTz-Cl, is designed and synthesized by bridging the benzobisthiazole acceptor block and chlorinated benzodithiophene donor block with thiophene units for application as an electron donor in all-PSCs. PBBTz-Cl not only possesses wide bandgap and deep energy levels but also displays strong absorption, high-planar structure, and good crystallinity, making it a promising candidate for application as a polymer donor in organic solar cells. When paired with the narrow bandgap polymer acceptor PY-IT, a fibril-like morphology forms, which facilitates exciton dissociation and charge transport, contributing to a power conversion efficiency (PCE) of 17.15% of the corresponding all-PSCs. Moreover, when introducing another crystalline polymer acceptor BTP-2T2F into the PBBTz-Cl:PY-IT host blend, the absorption ditch in the range of 600-750nm is filled, and the blend morphology is further optimized with the trap density reducing. As a result, the ternary blend all-PSCs achieve a significantly improved PCE of 18.60%, which is among the highest values for all-PSCs to date.

Developing Efficient Benzene Additives for 19.43% Efficiency of Organic Solar Cells by Crossbreeding Effect of Fluorination and Bromination

AbstractEmploying volatile solid additives have emerged as a promising method to optimize the morphology and improve the performance of organic solar cells (OSCs). However, principles governing the efficient design of solid additives remain elusive. Herein, the programmed fluorination and/or bromination on benzene core to develop efficient additives for OSCs is reported. The programmed fluorination and/or bromination endow the five halogen benzene derivatives, 1,3,5‐trifluorobenzene, hexafluorobenzene, 1,3,5‐tribromo‐2,4,6‐trifluorobenzene (TFTB), 1,3,5‐tribromobenzene, and hexabromobenzene, with different melting and boiling points, volatility, as well as interactions with the host blend. Studies indicate that the additives with extremely high and low volatility are almost powerless and even detrimental to the morphology evolution. Among them, the combination of fluorine and bromine atoms on TFTB not only enables the more appropriate m.p./b.p. and volatility, but also exerts stronger molecular interactions with the host blend, giving rise to higher ordered molecular packing and more favorable morphology. Importantly, TFTB exhibits good universality to optimize the performances of OSCs with high power conversion efficiencies (PCEs; over 18%) in a group of binary blend systems, and an impressive PCE of 19.43% in the ternary PBTz‐F:PM6:L8‐BO system.

Fabrication and characterizations of nanocomposite flexible films of ZnO and polyvinyl chloride/poly(N-vinyl carbazole) polymers for dielectric capacitors

Polymer-based energy storage has recently attracted the attention of researchers. Herein, via the sol–gel method, we prepared zinc oxide nanoparticles (ZnO NPs), as nanofiller up to 5 wt% filling levels, and a host polymeric blend matrix of polyvinyl chloride (PVC) and poly (N-vinyl carbazole) (PVK) were taken to synthesize nanocomposite films via the solution casting. The ratio of PVC: PVK was 90:10 wt%. The X-ray diffraction (XRD) results indicated that the prepared nanocomposite films’ crystallinity decreased as ZnO NPs content increased; it decreased from 54.23 to 22.14 %. The scanning electron microscope (SEM) micrographs revealed good miscibility of the prepared PVC/PVK blend and the homogeneous distribution of ZnO NPs within the host blend matrix. The thermal stability of the prepared nanocomposites was studied through the TGA technique, and the thermal activation energy was calculated using the Coats-Redfern method. In the optical results, the optical absorption spectra revealed that the energy gap for the allowed direct transition reduced under adding ZnO NPs; it reduced from 3.61 eV for the pure PVC/PVK blend to 2.96 eV for the nanocomposite film with ZnO nanofiller content of 5 wt%. AC conductivity experiments revealed that the electrical/dielectric properties of the nanocomposite films get enhanced by increasing the ZnO NPs content. Following the incorporation of the ZnO NPs, the AC electrical conductivity (σac), dc electrical conductivity (σdc), dielectric constant (ε′), and dielectric loss (ε″) values of PVC/PVK/ZnO nanocomposite films get improved; the σdc values increased from 6.46 × 10−16 S/cm for the blend PVC/PVK matrix to 3.63 × 10−13 S/cm for nanocomposites with ZnO NPs content of 5 wt%. Additionally, both ε′ and ε″ values increased while increasing the ZnO NPs content. These findings could suggest that the prepared PVC/PVK/ZnO nanocomposite films could be a promise for the applications of dielectric energy storage polymer-based capacitors.

A modeling approach to understanding OLED performance improvements arising from spatial variations in guest:host blend ratio.

Phosphorescent organic light emitting diodes (OLEDs) suffer from efficiency roll off, where device efficiency rapidly decays at higher luminance. One strategy to minimize this loss of efficiency at higher luminance is the use of non-uniform or graded guest:host blend ratios within the emissive layer. This work applies a multi-scale modeling framework to elucidate the mechanisms by which a non-uniform blend ratio can change the performance of an OLED. Mobility and exciton data are extracted from a kinetic Monte-Carlo model, which is then coupled to a drift diffusion model for fast sampling of the parameter space. The model is applied to OLEDs with uniform, linear, and stepwise graduations in the blend ratio in the emissive layer. The distribution of the guests in the film was found to affect the mobility of the charge carriers, and it was determined that having a graduated guest profile broadened the recombination zone, leading to a reduction in second order annihilation rates. That is, there was a reduction in triplet-triplet and triplet-polaron annihilation. Reducing triplet-triplet and triplet-polaron annihilation would lead to an improvement in device efficiency.

Structural, Optical, and Electrical Parameters of Doped PVA/PVP Blend with TPAI or THAI Salt.

The 70% polyvinyl alcohol/30% polyvinyl pyrrolidone (PVA/PVP) polymer blends, with different weight ratios of tetrapropylammonium iodide (TPAI) or tetrahexylammonium iodide (THAI) salt, were prepared using dimethyl sulfoxide (DMSO) as a solvent. The X-ray diffraction technique was used to trace the crystalline nature of the formed blends. The SEM and EDS techniques were applied to figure out the morphology of the blends. The variation in the FTIR vibrational bands was used to investigate the chemical composition and the effect of different salt doping on the functional groups of the host blend. The influence of the salt type (TPAI or THAI) and its ratio on the linear and nonlinear optical parameters for the doped blends were investigated in detail. Absorbance and reflectance are highly enhanced in the UV region reaching a maximum for the blend with 24% TPAI or THAI; so, it can be employed as shielding materials for UVA and UVB types. The direct (5.1 eV) and indirect (4.8 eV) optical bandgaps were reduced continuously to (3.52, 3.63 eV) and (3.45, 3.51 eV) while increasing the content of TPAI or THAI, respectively. The blend doped with 24% wt TPAI exhibited the highest refractive index (around 3.5 in 400-800 nm). The DC conductivity is affected by the content and type of salt, its dispersion, and blend-salt interaction. The activation energies of different blends were obtained by applying the Arrhenius formula.