Free-radical Crosslinking Copolymerization Research Articles

Temperature-Regulated Synthesis of Hyaluronic Acid-Interpenetrated Polyacrylamide/Poly(Acrylic Acid Sodium Salt) Semi-Interpenetrated Polymer Network Gel for the Removal of Methyl Violet.

An alternative synthetic pathway was proposed for the optimization of synthesis to find a better correlation between the swelling and elasticity of hyaluronic acid-interpenetrated gels via temperature regulation. An experimental design methodology was presented for the synthesis of polyacrylamide/poly(acrylic acid sodium salt)/hyaluronic acid, PAAm/PSA/HyA, gels by modifying the one-pot procedure using free radical crosslinking copolymerization of AAm with the addition of anionic linear PSA chains in the presence of various amount of HyA, ranging between 0.05% and 0.20% (w/v). Semi-interpenetrated polymer network (IPN)-structured gels were designed with tunable elasticity, in which the extent of covalent crosslinking interactions is controlled by polymerization temperature ranging between -18 and 45 °C. Depending on the HyA content added in the synthesis and the polymerization temperature, the swelling ratio could be controlled. The addition of 0.05% (w/v) HyA increased the swelling of semi-IPNs, while the elastic modulus increased with increasing HyA content and decreased with the polymerization temperature. PAAm/PSA/HyA semi-IPNs showed the typical pH-sensitive swelling of anionic gels, and the swelling reached a maximum at a pH of 11.2. PAAm/PSA/HyA gels were tested for the removal of methyl violet from wastewater. Adsorption kinetics were shown to be well-fitted with the pseudo-second-order model using linear and nonlinear regression analysis. With the clear relationship between increased modulus and composition, this study enabled the fine-tuning of semi-IPN interactions by varying the polymerization temperature.

Randomly cross-linked amphiphilic copolymer networks of n-butyl acrylate and N,N-dimethylacrylamide: synthesis and characterization

Abstract Five randomly cross-linked amphiphilic copolymer networks (ACPN) were prepared via the free radical cross-linking copolymerization of the hydrophobic n-butyl acrylate (BuA) and the hydrophilic N,N-dimethylacrylamide (DMAAm), in the presence of a small amount (5 mol% with respect to the sum of BuA plus DMAAm monomers) of the hydrophobic 1,6-hexanediol diacrylate (HexDA) cross-linker, initiated by 4,4ʹ-azobis(4-cyanovaleric acid) in 1,4-dioxane at a 10 % w/v total monomer concentration. The five ACPNs differed in their BuA content, fixed at 10, 30, 50, 70 and 90 mol%. The two homopolymer networks, BuA and DMAAm, were also prepared using the same polymerization method. Thus, this study involved a total of seven polymer networks, forming a homologous series with BuA contents ranging from 0 to 100 mol%. These networks were characterized in terms of their degrees of swelling in tetrahydrofuran (THF) and water, their mechanical properties in water, and their adhesion to human skin. The degrees of swelling (DS) of the networks in THF were higher than those in water because THF is a non-selective solvent, whereas water is selective for the hydrophilic DMAAm units. The DSs in THF increased with the network content in the less polar BuA units, while the opposite was true for the DSs in water which decreased with the content in the hydrophobic BuA units from 11 (0 mol% BuA) down to 1.1 (100 mol% BuA). A maximum in the elastic modulus was observed for the hydrogel with 50 mol% BuA, reflecting the opposing effects of polymer composition in soft polymer (polyBuA) content and hydrogel water content. In contrast, the tensile strain at break increased monotonically with the hydrogel BuA content, reaching a remarkable ∼900 % for the hydrogel with 90 mol% BuA. Finally, the adhesion of the ACPNs, both in their dried and hydrated states, onto human skin was explored. The adhesion of the hydrated samples onto skin was stronger than that of the dried ones. The hydrated ACPN with 30 mol% BuA exhibited the strongest adhesion onto skin, attributable to the best combination of a rather high content in polar DMAAm units (70 mol%), and a rather low aqueous DS (∼2.5), with the low DS value causing only a small dilution in the DMAAm units participating in the polar interactions with skin. The present work demonstrates that, even in this synthetically simple ACPN system, the multiple effects of ACPN composition on a certain property, in some cases opposing and in some other cooperating, lead to a rather complicated behavior. In particular, as the BuA content increases, some properties display maxima (elastic modulus, stress at break and fracture energy of hydrated ACPNs, and adhesion of hydrated ACPNs onto skin) while some other properties exhibit monotonic increases (strain at break of hydrated ACPNs, and adhesion of dried ACPNs onto skin). Thus, the optimal ACPN for a particular application will highly depend on the property best-serving the particular application, e.g., the ACPNs with 30, 50 and 90 mol% BuA for strongest wet adhesion to skin, stiffest hydrogel response, and highest hydrogel extensibility and toughness, respectively.

The Effect of Pyranine and MoS2 Content on the Optical Properties of Polyacrylamide-MoS2 Composite Gels

The most favorable members of the class of two-dimensional (2D) materials, molybdenum sulfide (MoS2), graphene, and tungsten disulfide (WS2) have become a thriving research frontier for many applications, ranging from catalysis to optoelectronic devices, due to their superior electronic behavior and mechanical properties. Making a new, smart, hydrogel when incorporating MoS2 into basic hydrogels can change their optical, electronic, and mechanical properties. In this work, MoS2-doped polyacrylamide (PAAm) gels were prepared via the free radical crosslinking copolymerization technique at room temperature without pyranine which is often used for crosslinking PAAm. The optical properties of PAAm-MoS2 composite gels were investigated, and they were analyzed using ultraviolet (UV) and fluorescence spectroscopy. The absorbance was measured before and after diffusion of MoS2-doped PAAm, and after the release of pyranine in and out of the composite gel, respectively. The shift of the absorption edge toward shorter wavelengths was seen when the quantity of MoS2 in the PAAm composite gels was decreased. The constituents included in the polymer composites exhibited notable photon energy absorption within the visible and ultraviolet spectra. This absorption phenomenon induced electron transitions to states of elevated energy. Parameters, such as refractive index and extinction coefficient, were analyzed with respect to the content of MoS2. When the MoS2 amount was increased in the gels, the percentage of reflectance increased. The extinction coefficient increased at longer wavelength and it decreased in the UV range, the shorter wavelength region. The results suggested that MoS2-doped PAAm composite gels show promising optoelectronic properties for developing optoelectronic devices.

Polyampholyte Hydrogels with pH-Dependent Swelling for Controlled Catch and Release of Model Dyes

Polyampholyte hydrogels with tunable charge are synthesized by a facile two-step approach including the free-radical crosslinking copolymerization of tert-butoxycarbonylaminomethylacrylate (tBAMA) with N,N′-methylenebisacrylamide and subsequent deprotection. Thermal, photo- and redox-initiating methods were utilized in the synthesis of crosslinked PtBAMA and the resulting polymer networks swell during deprotection in a mixture of trifluoro acetic acid/water. While the crosslinked PtBAMA forms organogels in various organic solvents such as chloroform, acetone and DMSO, polydehydroalanine (PDha) networks after deprotection form hydrogels with pH-dependent swelling and oscillatory swelling/deswelling depending on pH value and salinity. The tunable charge of the developed hydrogels was employed for a catch-and-release platform controlled by pH, in which methylene blue as a cationic model was adsorbed at pH 11 and desorbed at pH 2, whereas methyl blue as an anionic model dye was adsorbed at pH 2 and desorbed at pH 11.

An Early Study on the Synthesis of Lignin-Graft-(Net-Poly(acrylamide-co-N,N′methylenebisacrylamide)), Characterization of the Produced Copolymer, and Evaluation of Its Performance as Adsorbent for Lead Removal from Wastewater Purposes

A lignin-graft-(net-poly(acrylamide-co-N,N′methylenebisacrylamide)) copolymer was synthesized by conventional free-radical crosslinking copolymerization using conventional and microwave heating. Grafting of the polymer network onto lignin was confirmed by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR), scanning electron microscopy (SEM)/energy dispersive spectroscopy (EDS), thermogravimetric analysis (TGA), and elemental analysis. The performance of the modified materials for the removal of lead from water was evaluated. The materials obtained by the two types of heating showed excellent removal efficiencies: sample HLigAM4h, 96%; and sample HLigAMMW5, 86%. The maximum adsorption capacity of HLigAM4h was 209.82 mg g−1. The obtained copolymer (sample HLigAM4h) was characterized by X-ray photoelectron spectroscopy (XPS) and SEM/EDS after its evaluation as an adsorbent, which confirm the adsorption of Pb2+. This is the first of a series of studies on the topic, of a preliminary nature, with several other ones coming up in due time.

Mechanically Strong Superabsorbent Terpolymer Hydrogels Based on AMPS via Hydrogen-Bonding Interactions

Polymers based on 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) attract significant attention due to their large water absorption capacity when swollen in water. Poly(AMPS) (PAMPS) hydrogels are usually synthesized via free-radical cross-linking copolymerization of AMPS and a chemical cross-linker in aqueous solutions. Owing to the covalently cross-linked network structure of PAMPS hydrogels preventing dissipation of the crack energy, they exhibit poor mechanical properties. Herein, we demonstrate that the terpolymerization of AMPS, methacrylic acid (MAAc), and N,N-dimethylacrylamide (DMAA) in an aqueous solution under UV light without a chemical cross-linker produces mechanically strong hydrogen-bonded hydrogels that are durable in water. The terpolymer hydrogels formed at a MAAc/DMAA molar ratio of 4:1 exhibit a high Young’s modulus (26 ± 2 MPa) and toughness (31 ± 5 MJ·m–3) and are able to absorb 2035 ± 255 times their mass in water without dissolving. The water content at the gel preparation, denoted by w, significantly affects the microstructure of terpolymer hydrogels. Decreasing the water content w at gelation increases the length of the primary chains forming the three-dimensional (3D) network and hence the number of interchain H-bonds due to the proximity effect. An optically transparent-to-opaque transition accompanied with a strong-to-weak transition in the mechanical properties was detected with increasing w due to the transformation of the uniform network into a colloidal network composed of phase-separated and highly hydrogen-bonded AMPS-poor aggregates interconnected by AMPS-rich terpolymer chains.

Optical and mechanical properties of PNIPAm‐MWCNTs and PNIPAm‐GO composites

AbstractThe aim of this study is to investigate drying, swelling, elastic properties, and to produce optical band gap energies on the performance of Poly (N‐Isopropyl acrylamide) ‐ Multi walled carbon nanotubes (PNIPAm – MWCNTs) and Poly (N‐Isopropyl acrylamide)‐ Graphene Oxide (PNIPAm‐GO) composites, respectively. The composites were prepared by free radical crosslinking copolymerization. Drying and swelling of PNIPAm‐MWCNTs and PNIPAm‐ GO composites were performed by using steady state fluorescence technique. Firstly, the desorption coefficients of the composites were modeled by using Fick's Law. Cooperative diffusion coefficients were calculated by employing Li‐Tanaka Model. When composite doped with 10 wt% of MWCNTs has a higher desorption coefficient than composite doped with the same amount of GO, 40 wt% of GO content in the PNIPAm has a higher diffusion coefficient than the composite that has 40 wt% of MWCNTs content in the swelling process. Secondly, the composite that has 40 wt% of MWCNTs content has a higher modulus before swelling than the composite that has the same amount of GO contents. Lastly, optical band gap energies were calculated by using Tauc's approach, and Urbach's relation by using the data performed UV Spectroscopy. We found that PNIPAm ‐GO has a much narrower band gap value.

2D Materials (WS2, MoS2, MoSe2) Enhanced Polyacrylamide Gels for Multifunctional Applications.

Multifunctional polymer composite gels have attracted attention because of their high thermal stability, conductivity, mechanical properties, and fast optical response. To enable the simultaneous incorporation of all these different functions into composite gels, the best doping material alternatives are two-dimensional (2D) materials, especially transition metal dichalcogenides (TMD), which have been used in so many applications recently, such as energy storage units, opto-electronic devices and catalysis. They have the capacity to regulate optical, electronic and mechanical properties of basic molecular hydrogels when incorporated into them. In this study, 2D materials (WS2, MoS2 and MoSe2)-doped polyacrylamide (PAAm) gels were prepared via the free radical crosslinking copolymerization technique at room temperature. The gelation process and amount of the gels were investigated depending on the optical properties and band gap energies. Band gap energies of composite gels containing different amounts of TMD were calculated and found to be in the range of 2.48–2.84 eV, which is the characteristic band gap energy range of promising semiconductors. Our results revealed that the microgel growth mechanism and gel point of PAAm composite incorporated with 2D materials can be significantly tailored by the amount of 2D materials. Furthermore, tunable band gap energies of these composite gels are crucial for many applications such as biosensors, cartilage repair, drug delivery, tissue regeneration, wound dressing. Therefore, our study will contribute to the understanding of the correlation between the optical and electronic properties of such composite gels and will help to increase the usage areas so as to obtain multifunctional composite gels.

Synthesis and Characterization of Stretchable Ionic Cable

A transparent and flexible polymer with unique electric and sound signal transmission capability under highly stretchable conditions has been synthesized. In this paper the milestone achieved in the polymerization of intrinsic ionic Ω–conjugated polymer, hereinafter known as Ionic Cables (ICs), through free radical crosslinking co-polymerization process/technique and structural modifications encountered so far in our experiments are discussed. EIS and stress-strain assessments had showed that ionic conductivity and flexibility are dependent on the amount of accelerator Tetramethylethylenediamine (TEMED) and curing time (CT). By varying the amount of accelerator, in our case TEMED, and CT the ICs with ionic conductivity of 0.021 S/cm to 0.111S/cmand 350% elongation to 448% elongation conditions was synthesized with highly water absorption capability up to 78% of its total volume. The synthesized ICs with ultra-stretchability, transparency and conductivity can be used in versatile applications, including stretchable ionic cables, tissue engineering, ionic mass transport systems and bio sensors.

In Situ RheoNMR Correlation of Polymer Segmental Mobility with Mechanical Properties during Hydrogel Synthesis.

Understanding polymer gelation over multiple length‐scales is crucial to develop advanced materials. An experimental setup is developed that combines rheological measurements with simultaneous time‐domain 1H NMR relaxometry (TD‐NMR) techniques, which are used to study molecular motion (<10 nm) in soft matter. This so‐called low‐field RheoNMR setup is used to study the impact of varying degrees of crosslinking (DC) on the gelation kinetics of acrylic acid (AAc) and N,N′‐methylene bisacrylamide (MBA) free radical crosslinking copolymerization. A stretched exponential function describes the T 2 relaxation curves throughout the gelation process. The stretching exponent β decreases from 0.90 to 0.67 as a function of increasing DC, suggesting an increase in network heterogeneity with a broad T 2 distribution at higher DC. The inverse correlation of the elastic modulus G′ with T 2 relaxation times reveals a pronounced molecular rigidity for higher DC at early gelation times, indicating the formation of inelastic, rigid domains such as crosslinking clusters. The authors further correlate G′ with the polymer concentration during gelation using a T 1 filter for solvent suppression. A characteristic scaling exponent of 2.3 is found, which is in agreement with theoretical predictions of G′ based on the confining tube model in semi‐dilute entangled polymer solutions.

Evaluation of the fractal dimension of polyacrylamide during gelation and swelling

The photon scattering method was performed to monitor the free radical crosslinking copolymerization (FCC) of acrylamide (AAm) applied with N,N′-methylenebis (acrylamide) (Bis) in time. FCC experiments were conducted using different Bis contents to create fractal-like network structures in polyacrylamide (PAAm) gels. Higher intensity values of the scattered photons, Isc were observed with increasing Bis content, BC, at a given time, which was attributed to fractal-like macrogel formation from interconnected microgels. The same gels were used in swelling experiments after drying, and increased Isc intensities from the PAAm gels were observed during the swelling process. Fractal dimensions, d during the gelation and swelling processes were measured and found to be increased as gelation and swelling times increased. According to the results obtained from the gelation measurements, it was seen that the fractal size, d, increased from very small values to 3.00. A similar increase in the range 1.00–1.66 was observed during swelling experiments.

Cross-linking of double oil-in-water-in-oil emulsions: A new way for fragrance encapsulation with tunable sustained release

This paper describes a new route to synthesize polymeric capsules with interesting and diverse diffusive and mechanical properties. Such capsules were obtained by free radical cross-linking copolymerization of the intermediate water phase of a double oil-in-water-in-oil (O/W/O) emulsion. Such a strategy allows separating the locus of polymerization from the fragrance- containing compartment. Indeed fragrance molecules are known to be reactive. The encapsulated species, also corresponding to the innermost oil, was a model fragrance composed of more than 10 various molecules usually used in perfumery. In a first step, the double emulsion containing a hydrophilic monomer, either Methacrylamide or Oligo(ethyleneglycol) methacrylate, and a hydrophilic cross-linker, either Tetra(ethyleneglycol) diacrylate or N,N-Methylene-bis-Acrylamide, was formulated. The influence of the cross-linker agent on the feasibility of the double emulsion was examined. Then, in a second part, the polymerization was performed. Four different systems of capsules were developed and compared in terms of diffusive and mechanical properties. We show that changing the monomer /cross-linker couple allowed modulating the capsule properties.

The Effect of Methacrylic Acid and Maleic Acid on the Isothermal Kinetics of Acrylic Acid Crosslinking Co-polymerization under Conventional and Microwave Heating

The kinetics of free-radical crosslinking co-polymerization (FRCCP) of acrylic acid (AA) with both methacrylic acid (MA) (PAMA hydrogel ) and maleic acid (MAL) (PAMAL hydrogel) was investigated under the conditions of isothermal conventional heating (CH) and under the conditions of microwave heating (MWH) with controlled cooling. The kinetics curves of FRCCP of PAMA and PAMAL hydrogels under the conditions of CH are described with the kinetics model of second order chemical reaction, whereas the kinetics curves under the conditions of CH are described with the kinetics model of Polany-Winger. It is proved that MWH leads to the changes in the rate of FRCCP and to the changes in the values of the kinetic parameters (activation energy (Ea) and pre-exponential factor (lnA). It was found the existence of relationship between the values of the kinetic parameters calculated for MWH and CH for PAMA and PAMAL hydrogel synthesis process, which is well-known as compensation effect. The effect of MWH on the kinetics of FRCCP for PAMA and PAMAL hydrogel formation were explained by applying the model of activation by selective energy transfer (SET). The changes in kinetics model, rate of FRCCP and kinetics parameters, caused with the MWH can found wide application in designing novel technologies for obtaining polymers and for synthesis of polymers with novel physico-chemical properties. The suggested mechanism of activation for polymerisation under the conditions of MWH also enables development of novel reaction systems and technologies for polymers productions.

Implementation of Carboxymethyl cellulose/Acrylic acid/ Titanium dioxide Nanocomposite Hydrogel in Remediation of Cd(II), Zn(II) and Pb(II) for Water treatment application

In this study Acrylic acid/ Carboxymethylcellulose/Titanium dioxide (AAc/CMC-TiO2) hydrogel nanocomposite was synthesized by free-radical crosslinking copolymerization via gamma radiation. It was characterized using FT-IR and swelling properties. The swelling percentage increases with increasing time until reaches a certain limiting value after 6h The synthesized nanocomposite was used as an adsorbent for remediation of Cd(II), Zn(II) and Pb(II) from aqueous solutions by the static adsorption technique. It was found that the optimum pH for the adsorption is 5 and the sorption process is carried out at a fast operating time, 30-40 min, for all investigated metal ions. It was also found that the metal ions sorption capacity decreases with increasing the dosage of AAc/CMC-TiO2 from 5 to 150 mg. A progressive increase in the metal ions sorption capacity was obtained with increasing the initial metal ion concentration from 0.01 to 0.05 mol L-1 and the saturation of the sorbent active sites was done at initial metal ions concentration at 0.1 mol L-1. No significant interference on the removal of Pb (II) in the presence of NaCl, Na-acetate, KCl, KNO3 and NH4Cl ions while a slight decrease in the removal of Cd (II)and Zn(II) was done. The pseudo-second-order kinetic model and Freundlich adsorption model describe well the kinetic and isotherm, respectively, of the adsorption process of the investigated ions.

Temperature Effect on the Elasticity of Acrylamide-n-Isopropylacrylamide Copolymers

ABSTRACTAcrylamide (AAm) – N-isopropylacrylamide (NIPA) copolymers were prepared via free radical crosslinking copolymerization with various weight percentages (wt%) of AAm and NIPA. The temperature dependence of the compressive elastic modulus, G, and toughness, UT, of the PAAm- NIPA copolymers due to a volume phase transition was found using a compressive testing technique. It was observed that the compressive elastic modulus increased comprehensively when the temperature was increased between 30°C and 60°C. The PAAm- NIPA copolymers presented higher values of the compressive elastic modulus than pure NIPA above the lower critical solution temperature (LCST) (NIPA exhibits a volume phase transition from hydrophilic to hydrophobic in water at 31°C) and their compressive elastic modulus and toughness had a strong temperature dependence.

Poly(Hydroxypropyl methacrylate-co-glycidyl methacrylate): Facile synthesis of well-defined hydrophobic gels containing hydroxy-functional methacrylates

A range of well-defined hydrophobic hydroxy-functional methacrylate-based gels has been synthesized by free-radical crosslinking copolymerization of the monomers Hydroxypropyl methacrylate (HPMA) and Glycidyl methacrylate (GMA). Particularly, the effect of the hydrophobic functional groups of the comonomer GMA on the elasticity and swelling properties was investigated in order to understand the exact interactions and the consequent changes in the physical characteristics of poly(Hydroxypropyl methacrylate-co-glycidyl methacrylate) P(HPMA-co-GMA) hydrogels as well as cryogels. In addition, measuring and understanding how to control the mechanical response of the resulting gels which usually refers to the resistance to failure by fracture or excessive deformation can help the targeted design of specific applications with extended functionality. In the light of the experimental findings, it was suggested that the studied system with the monomers HPMA and GMA containing both acrylic and epoxy groups provides the design and performance versatility required for the most demanding coating and resin applications.

Mechanical properties of graphene oxide–polyacrylamide composites before and after swelling in water

Polyacrylamide (PAAm) hydrogels have been proposed for use as promising biomaterials in biomedical and tissue engineering but their poor mechanical and water-retention properties have hindered their development. Graphene oxide (GO), an excellent nanofiller, was added to PAAm to produce mechanically strong GO–PAAm composites. The free radical crosslinking copolymerization method was used with GO content varying in the range between 5 and 50 µl of GO. The mechanical properties of the GO–PAAm composites are measured by compressive test, revealing a decrease in the shear modulus and toughness of the composites above 8 µl of GO by increasing GO content.

Elastic properties of a swollen polyacrylamide (PAAm) gel doped with various multiwalled carbon nanotube (MWNT) contents

Abstract The toughness UT and shear modulus S of polyacrylamide (PAAm) – multiwalled carbon nanotube (MWNTs) composites were studied with various MWNT contents. These composites were prepared via free radical crosslinking copolymerization with different amounts of MWNT varying in the range between 0.1 and 50 wt.-%. The MWNT content dependency of the shear modulus of the composites due to volume phase transition was measured using tensile testing at 30 °C. It was observed that the composite preserves the ability to undergo the volume phase transition and its elastic modulus is strongly dependent on the MWNT content. The observed shear modulus first increased and then decreased above 1 wt.-% MWNT content during such loading tests. The toughness showed exactly the reverse behavior dependent on the MWNT content, as compared to the elasticity and as expected.

Optical energy band gap of PAAm-GO composites

Graphene oxide (GO) can be used as an electron acceptor for polymers. The generation of the exciton in such materials is intimately related to the optical band gap. Polyacrylamide (PAAm) – graphene oxide (GO) composites were prepared via free radical crosslinking copolymerization with GO content varying in the range between 5 and 40µl of GO. The influence of the GO content on the optical properties of the composites is characterized by ultraviolet visible spectrophotometer. The optical band gap of the composite has been calculated by using Tauc’s model. The tail width of the localized states has been calculated by using Urbach’s relation, and the values of Urbach’s energy with the variation of GO have been found from 2,89 to 2,96eV. The results demonstrated that GO can be well dispersed in the PAAm-GO composites and consequently the optical band gap has been correlated with the various amounts of GO.

Role of ion conducting polymeric electrolyte in suppressing deterioration of cathode electrodes in dye-sensitized solar cells

In this study, an ion conducting polymeric hydrogel (ICPH) is synthesized, characterized and used as a matrix for trapping the electrolyte solution to suppress the deterioration of cathode electrodes for dye-sensitized solar cells (DSSCs). Polymeric hydrogels are synthesized as free radical cross-linking co-polymerization of acrylamide (AAm) and methylenebisacrylamide (BIS) as crosslink agent in slab forms with the same thickness. The polymer host is characterized by scanning electron microscopy (SEM). Impedance spectroscopy studies are carried out in the frequency range of 5 Hz–13 MHz at room temperature. It is observed that while the dielectric constant decreased, the loss tangents increased with increasing electrolyte content which is trapped in ICPH. The as-prepared ICPH/graphene electrodes, assembled with this material as cathode, are confirmed as substitution for platinum (Pt) counter electrode in DSSCs. The photovoltaic tests of the ICPH-DSSCs are carried out by the current–voltage (I–V) measurements and it is observed that ICPH-DSSC exhibited significantly enhanced electrical properties such as increased photovoltaic cell efficiency (PCE) which reached to 5.41% after using the ICPH. We predict that this work will open a way to fabricate the DSSC devices with a cathode electrode based on ion conductive polymeric hydrogels.