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The development of direct dimethyl ether (DME) solid oxide fuel cells (SOFCs) has several drawbacks, due to the low catalytic activity and carbon deposition of conventional Ni–zirconia-based anodes. In the present study, the insertion of 2.0 wt.% Ru-Ce0.7Zr0.3O2−δ (ruthenium–zirconium-doped ceria, Ru-CZO) as an anode catalyst layer (ACL) is proposed to be a promising solution. For this purpose, the CZO powder was prepared by the sol–gel synthesis method, and subsequently, nanoparticles of Ru (1.0–2.0 wt.%) were synthesized by the impregnation method and calcination. The catalyst powder was characterized by BET-specific surface area, X-ray diffraction (XRD), field emission scanning electron microscopy with an energy-dispersive spectroscopy detector (FESEM-EDS), and transmission electron microscopy (TEM) techniques. Afterward, the catalytic activity of Ru-CZO catalyst was studied using DME partial oxidation. Finally, button anode-supported SOFCs with Ru-CZO ACL were prepared, depositing Ru-CZO onto the anode support and using an annealing process. The effect of ACL on the electrochemical performance of cells was investigated under a DME and air mixture at 750 °C. The results showed a high dispersion of Ru in the CZO solid solution, which provided a complete DME conversion and high yields of H2 and CO at 750 °C. As a result, 2.0 wt.% Ru-CZO ACL enhanced the cell performance by more than 20% at 750 °C. The post-test analysis of cells with ACL proved a remarkable resistance of Ru-CZO ACL to carbon deposition compared to the reference cell, evidencing the potential application of Ru-CZO as a catalyst as well as an ACL for direct DME SOFCs. [ABSTRACT FROM AUTHOR]

Fuel cells have already demonstrated their potential for green energy generation. However, the low reaction performance becomes an obstacle in terms of large-scale commercial manufacturing. Accordingly, this work focuses on a new unique fabrication of three-dimensional pore hierarchy TiO2-graphene aerogel (TiO2-GA) supporting PtRu catalyst for anodic catalyst direct methanol fuel cell, which is facile, ecologically benign, and economical. In this work, a hydrothermal technique was used, followed by a freeze-drying technique and a microwave-assisted ethylene reduction technique. The structural properties of the studied materials were confirmed by UV/visible spectroscopy, XRD, Raman spectrum, FESEM TEM, and XPS. Based on existing structural advantages, the performance of PtRu/TiO2-GA has been investigated on DMFC anode catalysts. Furthermore, electrocatalytic stability performance with the same loading (~20%) was compared to commercial PtRu/C. Experimental outcomes show that the TiO2-GA support offered a significantly high surface area value of 68.44 m2g−1, mass activity/specific activity (608.17 mAmg−1/0.45 mA/cm2PtRu) that is higher than commercial PtRu/C (79.11 mAmg−1/0.19 mA/cm2PtRu). In passive DMFC mode, PtRu/TiO2-GA showed a maximum power density of 3.1 mW cm−2, which is 2.6 times higher than that of the PtRu/C commercial electrocatalyst. This suggests that PtRu/TiO2-GA has a promising possibility for methanol oxidation and may be used as an anodic element in DMFC. [ABSTRACT FROM AUTHOR]

Although direct methanol fuel cells (DMFCs) have been spotlighted in the past decade, their commercialization has been hampered by the poor efficiency of the methanol oxidation reaction (MOR) due to the unsatisfactory performance of currently available electrocatalysts. Herein, we developed a binder-free, copper-based, self-supported electrode consisting of a heterostructure of Cu3P and mixed copper oxides, i.e., cuprous–cupric oxide (Cu-O), as a high-performance catalyst for the electro-oxidation of methanol. We synthesized a self-supported electrode composed of Cu-O|Cu3P using a two-furnace atmospheric pressure–chemical vapor deposition (AP-CVD) process. High-resolution transmission electron microscopy analysis revealed the formation of 3D nanocrystals with defects and pores. Cu-O|Cu3P outperformed the MOR activity of individual Cu3P and Cu-O owing to the synergistic interaction between them. Cu3P|Cu-O exhibited a highest anodic current density of 232.5 mAcm−2 at the low potential of 0.65 V vs. Hg/HgO, which is impressive and superior to the electrocatalytic activity of its individual counterparts. The formation of defects, 3D morphology, and the synergistic effect between Cu3P and Cu-O play a crucial role in facilitating the electron transport between electrode and electrolyte to obtain the optimal MOR activity. Cu-O|Cu3P shows outstanding MOR stability for about 3600 s with 100% retention of the current density, which proves its robustness alongside CO intermediate. [ABSTRACT FROM AUTHOR]

Palladium (Pd) nanostructures are highly active non-platinum anodic electrocatalysts in alkaline direct methanol fuel cells (DMFCs), and their electrocatalytic performance relies highly on their morphology and composition. This study reports the preparation, characterizations, and electrocatalytic properties of palladium-copper alloys loaded on the carbon support. XC-72 was used as a support, and hydrazine hydrate served as a reducing agent. PdxCuy/XC-72 nanoalloy catalysts were prepared in a one-step chemical reduction process with different ratios of Pd and Cu. A range of analytical techniques was used to characterize the microstructure and electronic properties of the catalysts, including transmission electron microscopy (TEM), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma emission spectroscopy (ICP-OES). Benefiting from excellent electronic structure, Pd3Cu2/XC-72 achieves higher mass activity enhancement and improves durability for MOR. Considering the simple synthesis, excellent activity, and long-term stability, PdxCuy/XC-72 anodic electrocatalysts will be highly promising in alkaline DMFCs. [ABSTRACT FROM AUTHOR]

The diffusion layer (DL) in the structure of the membrane electrode assembly (MEA) of a micro direct methanol fuel cell (μDMFC) plays an essential role in reactant/product mass transfer and catalyst loading. The material selection and structure design of the μDMFC affects its performance. In this work, a reduced graphene oxide/carbon paper (rGO/CP) was proposed and prepared for the anode DL of a μDMFC. It was prepared using electrophoretic sedimentation combined with an in situ reduction method. The rGO/CP reduced the cell's ohmic and charge transfer resistances. Meanwhile, it provided more significant mass transfer resistance to reduce the methanol crossover, allowing the cell to operate stably at higher concentrations for a longer duration than conventional μDMFCs. The experimental results showed that the maximum power density increased by 53% compared with the traditional anode DL of carbon paper. [ABSTRACT FROM AUTHOR]

Pt-based alloy or bimetallic anode catalysts have been developed to reduce the carbon monoxide (CO) poisoning effect and the usage of Pt in direct methanol fuel cells (DMFCs), where the second metal plays a role as CO poisoning inhibitor on Pt. Furthermore, better performance in DMFCs can be achieved by improving the catalytic dispersion and using high-performance supporting materials. In this work, we introduced a free-standing, macroscopic, interwoven tubular graphene (TG) mesh as a supporting material because of its high surface area, favorable chemical inertness, and excellent conductivity. Particularly, binary AuPt nanoparticles (NPs) can be easily immobilized on both outer and inner walls of the TG mesh with a highly dispersive distribution by a simple and efficient chemical reduction method. The TG mesh, whose outer and inner walls were decorated with optimized loading of binary AuPt NPs, exhibited a remarkably catalytic performance in DMFCs. Its methanol oxidation reaction (MOR) activity was 10.09 and 2.20 times higher than those of the TG electrodes with only outer wall immobilized with pure Pt NPs and binary AuPt NPs, respectively. Furthermore, the catalyst also displayed a great stability in methanol oxidation after 200 scanning cycles, implying the excellent tolerance toward the CO poisoning effect. [ABSTRACT FROM AUTHOR]

The development of new synthetic methods for methanol-tolerant catalysts with improved performance is of fundamental importance for the commercialization of fuel cells. Herein, we reported a facile displacement reaction-assisted synthesis of graphene-supported sub-nanometer Pt/Bi catalysts (Pt/Bi/rGO). Bismuth (0) nanoparticles produced by NH3BH3 reduction can be further dissolved into the ethylene glycol, implying Bi(0) has a strong interaction with the hydroxyl group. That is the key interaction between Bi(0) and the functional group on the rGO to form the ultra-small Bi/rGO catalyst. Furthermore, Pt clusters are obtained by the displacement between Bi(0) and HPtCl4 and are directly anchored to the rGO surface. The as-synthesized Pt/Bi/rGO catalyst exhibits high oxygen reduction mass activity and high tolerance to methanol poisoning. In the presence of 0.5 mol/L CH3OH, the initial potential and activity of ORR were almost unchanged, which demonstrated great potential in the application of direct methanol fuel cells. [ABSTRACT FROM AUTHOR]

For micro direct methanol fuel cell (μDMFC), water flooding on the cathode seriously affects the performance stability. Additionally, the effect of material and wettability of the cathode current collector (CCC) on the drainage capacity is studied to improve the μDMFC's performance. To this end, a CCC with foamed stainless steel was prepared to assemble the μDMFC due to its absorbency. Further, based on analyzing the gas–liquid two-phase flow characteristics of the μDMFC cathode, it was found that the gradient wettability CCC could accelerate the discharge of cathode water. Hence, the foam stainless steel CCC was partially immersed in a KOH solution to complete the gradient corrosion using its capillary force. Then, four different types of gradient wettability CCC were prepared by controlling the time of chemical corrosion. Finally, the performance of the μDMFC with different gradient wettability CCC was tested at room temperature using electrochemical impedance spectroscopy (EIS) and discharge voltage. The experimental results show that the gradient wettability CCC can improve the performance of the μDMFC by slowing down the rate of cathode flooding. The optimum corrosion time is 5 min at a concentration of 1 mol/L. Under these conditions, the CCC has the best gradient wettability, and the μDMFC has the lowest total impedance. The discharge voltage of the μDMFC with corroded CCC is increased by 33.33% compared to the uncorroded CCC μDMFC. The gradient wettability CCC designed in this study is economical, convenient, and practical for water management of the μDMFC. [ABSTRACT FROM AUTHOR]

In this work, palladium-nickel nanoparticles supported on carbon nanofibers were synthesized, with metal contents close to 25 wt % and Pd:Ni atomic ratios near to 1:2. These catalysts were previously studied in order to determine their activity toward the oxygen reduction reaction. Before the deposition of metals, the carbon nanofibers were chemically treated in order to generate oxygen and nitrogen groups on their surface. Transmission electron microscopy analysis (TEM) images revealed particle diameters between 3 and 4 nm, overcoming the sizes observed for the nanoparticles supported on carbon black (catalyst Pd-Ni CB 1:2). From the CO oxidation at different temperatures, the activation energy Eact for this reaction was determined. These values indicated a high tolerance of the catalysts toward the CO poisoning, especially in the case of the catalysts supported on the non-chemically treated carbon nanofibers. On the other hand, apparent activation energy Eap for the methanol oxidation was also determined finding—as a rate determining step—the COads diffusion to the OHads for the catalysts supported on carbon nanofibers. The results here presented showed that the surface functional groups only play a role in the obtaining of lower particle sizes, which is an important factor in the obtaining of low CO oxidation activation energies. [ABSTRACT FROM AUTHOR]

The present work investigates the direct mixing of aqueous zeolitic imidazolate framework-8 (ZIF-8) suspension into a polyvinyl alcohol (PVA) and crosslinked with glutaraldehyde (GA) to form swelling-resistant, mechanically robust and conductivity retentive composite membranes. This drying-free nanofiller incorporation method enhances the homogeneous ZIF-8 distributions in the PVA/ZIF-8/GA composites to overcome the nanofiller aggregation problem in the mixed matrix membranes. Various ZIF-8 concentrations (25.4, 40.5 and 45.4 wt.%) are used to study the suitability of the resulting GA-crosslinked composites for direct alkaline methanol fuel cell (DAMFC). Surface morphological analysis confirmed homogeneous ZIF-8 particle distribution in the GA-crosslinked composites with a defect- and crack-free structure. The increased ionic conductivity (21% higher than the ZIF-free base material) and suppressed alcohol permeability (94% lower from the base material) of PVA/40.5%ZIF-8/GA resulted in the highest selectivity among the prepared composites. In addition, the GA-crosslinked composites' selectivity increased to 1.5–2 times that of those without crosslink. Moreover, the ZIF-8 nanofillers improved the mechanical strength and alkaline stability of the composites. This was due to the negligible volume swelling ratio (<1.4%) of high (>40%) ZIF-8-loaded composites. After 168 h of alkaline treatment, the PVA/40.5%ZIF-8/GA composite had almost negligible ionic conductivity loss (0.19%) compared with the initial material. The maximum power density (Pmax) of PVA/40.5%ZIF-8/GA composite was 190.5 mW cm−2 at 60 °C, an increase of 181% from the PVA/GA membrane. Moreover, the Pmax of PVA/40.5%ZIF-8/GA was 10% higher than that without GA crosslinking. These swelling-resistant and stable solid electrolytes are promising in alkaline fuel cell applications. [ABSTRACT FROM AUTHOR]

Although sheet-like materials have good electrochemical properties, they still suffer from agglomeration problems during the electrocatalytic process. Integrating two-dimensional building blocks into a hollow cage-like structure is considered as an effective way to prevent agglomeration. In this work, the hierarchical NiCo2O4 nanocages were successfully synthesized via coordinated etching and precipitation method combined with a post-annealing process. The nanocages are constructed through the interaction of two-dimensional NiCo2O4 nanosheets, forming a three-dimensional hollow hierarchical architecture. The three-dimensional supporting cavity effectively prevents the aggregation of NiCo2O4 nanosheets and the hollow porous feature provides amounts of channels for mass transport and electron transfer. As an electrocatalytic electrode for methanol, the NiCo2O4 nanocages-modified glassy carbon electrode exhibits a lower overpotential of 0.29 V than those of NiO nanocages (0.38 V) and Co3O4 nanocages (0.34 V) modified glassy carbon electrodes. The low overpotential is attributed to the prominent electrocatalytic dynamic issued from the three-dimensional hollow porous architecture and two-dimensional hierarchical feature of NiCo2O4 building blocks. Furthermore, the hollow porous structure provides sufficient interspace for accommodation of structural strain and volume change, leading to improved cycling stability. The NiCo2O4 nanocages-modified glassy carbon electrode still maintains 80% of its original value after 1000 consecutive cycles. The results demonstrate that the NiCo2O4 nanocages could have potential applications in the field of direct methanol fuel cells due to the synergy between two-dimensional hierarchical feature and three-dimensional hollow structure. [ABSTRACT FROM AUTHOR]

It is of prime importance to develop anode electrocatalysts for direct methanol fuel cells (DMFCs) with good performance, which is critical for their commercial applications. Metal-organic framework (MOF)-derived carbon materials are extensively developed as supports of catalysts. Herein, Co embedded nitrogen-doped carbon nanotube hollow porous carbon (Co-NCNT-HPC) derived from MOFs have been fabricated, which were synthesized by pyrolyzing at an optimized temperature of 800 °C using ZIF-8@ZIF-67 as a precursor. The presence of ZIF-8@ZIF-67 ensures the doping of nitrogen and the large specific surface area of the support materials at high temperatures. A Pt/Co-NCNT-HPC800 sample, which was synthesized using Co-NCNT-HPC800 as a support, showed an enhanced mass activity of 416.2 mA mg−1Pt for methanol oxidation reaction (MOR), and the onset potential of COad oxidation of 0.51 V, which shifted negatively about 0.13 V compared with Pt/C (20%). Moreover, the Pt/Co-NCNT-HPC800 sample exhibits high stability. This work provides a facile strategy for MOF-derived carbon materials to construct advanced electrocatalysts for MOR. [ABSTRACT FROM AUTHOR]

Platinum (Pt) is widely used as an activator in direct methanol fuel cells (DMFCs). However, the development of Pt catalyst is hindered due to its high cost and CO poisoning. A multi-metallic catalyst is a promising catalyst for fuel cells. We develop a simple and rapid method to synthesize PtNiCo/rGO nanocomposites (NCs). The PtNiCo/rGO NCs catalyst was obtained by microwave-assisted synthesis of graphene oxide (GO) with Pt, Ni, and Co precursors in ethylene glycol (EG) solution after heating for 20 min. The Pt-Ni-Co nanoparticles showed a narrow particle size distribution and were uniformly dispersed on the reduced graphene oxide without agglomeration. Compared with PtNiCo catalyst, PtNiCo/rGO NCs have superior electrocatalytic properties, including a large electrochemical active surface area (ECSA), the high catalytic activity of methanol, excellent anti-toxic properties, and high electrochemical stability. The ECSA can be up to 87.41 m2/g at a scan rate of 50 mV/s. They also have the lowest oxidation potential of CO. These excellent electrochemical performances are attributed to the uniform dispersion of PtNiCo nanoparticles, good conductivity, stability, and large specific surface area of the rGO carrier. The synthesized PtNiCo/rGO nanoparticles have an average size of 17.03 ± 1.93 nm. We also investigated the effect of catalyst material size on electrocatalytic performance, and the results indicate that PtNiCo/rGO NC catalysts can replace anode catalyst materials in fuel cell applications in the future. [ABSTRACT FROM AUTHOR]

Recently, alkaline direct methanol fuel cells have made great progress with the development of alkaline electrocatalysis, and a wide variety of catalysts have been explored for methanol oxidation reaction (MOR)and oxygen reduction reaction (ORR). However, the slow kinetics of the MOR and ORR remain a great challenge. In this paper, self-supported defect-rich AuCu was obtained by a convenient one-pot strategy. Self-supported AuCu presented a branched, porous nanostructure. The nanobranch consisted of several 13 nm skeletons, which connected in the kink of the structure. Different growth directions co-existed at the kink, and the twin boundaries and dislocations as defects were observed. When the Au-based nanostructure functioned as an electrocatalyst, it showed robust MOR and ORR performance. For the MOR, the forward peak current was 2.68 times greater than that of Au/C; for the ORR, the activity was close to that of Pt/C and significantly better than that of Au/C. In addition, it possessed superior electrochemical stability for MOR and ORR. Finally, an in-depth exploration of the impact of surface defects and electrochemical Cu removal on MOR and ORR activity was carried out to explain the MOR and ORR's catalytic performance. [ABSTRACT FROM AUTHOR]

Direct urea fuel cells (DUFCs) have recently drawn increased attention as sustainable power generation devices because of their considerable advantages. Nonetheless, the kinetics of the oxidation-reduction reaction, particularly the electrochemical oxidation and oxygen reduction reaction (ORR), in direct urea fuel cells are slow and hence considered to be inefficient. To overcome these disadvantages in DUFCs, Pd nanoparticles loaded onto Co3O4 supported by multi-walled carbon nanotubes (Pd/Co3O4@MWCNT) were employed as a promising cathode catalyst for enhancing the electrocatalytic activity and oxygen reduction reaction at the cathode in DUFCs. Co3O4@MWCNT and Pd/Co3O4@MWCNT were synthesized via a facile two-step hydrothermal process. A Pd/MWCNT catalyst was also prepared and evaluated to study the effect of Co3O4 on the performance of the Pd/Co3O4@MWCNT catalyst. A current density of 13.963 mA cm−2 and a maximum power density of 2.792 mW cm−2 at 20 °C were obtained. Pd/Co3O4@MWCNT is a prospectively effective cathode catalyst for DUFCs. The dilution of Pd with non-precious metal oxides in adequate amounts is economically conducive to highly practical catalysts with promising electrocatalytic activity in fuel cell applications. [ABSTRACT FROM AUTHOR]

Controlled deposition of metals is essential for the creation of bimetallic catalysts having predictable composition and character. Continuous co-electroless deposition (co-ED) permits the creation of bimetallic catalysts with predictive control over composition. This method was applied to create a suite of Cu–Pt mixed-metal shell catalysts for use in methanol electrooxidation in direct methanol fuel cell applications (DMFCs). Enhanced performance of Cu–Pt compositions over Pt alone was predicted by existing computational studies in the literature. Experimental evidence from this study supports the bifunctional catalyst explanation for enhanced activity and confirms the optimum Cu:Pt ratio as Cu3Pt for this methanol electrooxidation. This ability to control the composition of a bimetallic shell can be extended to other systems where the ratio of two metals is critical for catalytic performance. [ABSTRACT FROM AUTHOR]

In order to obtain biopolymer chitosan-based proton exchange membranes with excellent mechanical properties as well as high ionic conductivity at the same time, natural attapulgite (AT) with one-dimensional (1D) structure was loaded with a strong heteropolyacid and also a super proton conductor, phosphotungstic acid (PWA), using a facial method. The obtained PWA anchored attapulgite (WQAT) was then doped into the chitosan matrix to prepare a series of Chitosan (CS)/WQAT composite membranes. The PWA coating could improve the dispersion and interfacial bonding between the nano-additive and polymer matrix, thus increasing the mechanical strength. Moreover, the ultra-strong proton conduction ability of PWA together with the interaction between positively charged CS chains and negatively charged PWA can construct effective proton transport channels with the help of 1D AT. The proton conductivity of the composite membrane (4 wt.% WQAT loading) reached 35.3 mS cm−1 at 80 °C, which was 31.8% higher than that of the pure CS membrane. Moreover, due to the decreased methanol permeability and increased conductivity, the composite membrane with 4% WQAT content exhibited a peak power density of 70.26 mW cm−2 fed at 2 M methanol, whereas the pure CS membrane displayed only 40.08 mW cm−2. [ABSTRACT FROM AUTHOR]

In this work a novel bimetallic nickel oxide/copper oxide metal–organic framework (NiO/CuO MOF) has been developed by using two linkers: Benzene Dicarboxylic acid (BDC) and Pyrazine. The composites of NiO/CuO MOF with different amounts of reduced graphene oxide (rGO) were synthesized through a hydrothermal method and subsequently characterized by multiple significant techniques like XRD, SEM, EDX, FTIR and Raman IR for an investigation of their structural and morphological properties. The prepared series of material was later employed for electrochemical oxidation of methanol, tested by cyclic voltammetry (CV) in basic medium on a modified glassy carbon electrode (GCE). The electrochemical response depicts that increasing concentration of rGO enhances the electrocatalytic activity of the catalyst for methanol oxidation reaction (MOR). The catalyzed oxidation reaction of methanol by NiO/CuO MOF and rGO-NiO/CuO MOF composites give a superlative current density of 437. 28 mA/cm2 at 0.9 V potential at 50 mV/s scan rate. This activity makes it a promising catalytic material for electrolysis of methanol in direct methanol fuel cell (DMFC). [ABSTRACT FROM AUTHOR]

The behavior of supported alloyed and de-alloyed platinum-copper catalysts, which contained 14–27% wt. of Pt, was studied in the reactions of methanol electrooxidation (MOR) and oxygen electroreduction (ORR) in 0.1 M HClO4 solutions. Alloyed PtCux/C catalysts were prepared by a multistage sequential deposition of copper and platinum onto a Vulcan XC72 dispersed carbon support. De-alloyed PtCux−y/C catalysts were prepared by PtCux/C materials pretreatment in acid solutions. The effects of the catalysts initial composition and the acid treatment condition on their composition, structure, and catalytic activity in MOR and ORR were studied. Functional characteristics of platinum-copper catalysts were compared with those of commercial Pt/C catalysts when tested, both in an electrochemical cell and in H2/Air membrane-electrode assembly (MEA). It was shown that the acid pretreatment of platinum-copper catalysts practically does not have negative effect on their catalytic activity, but it reduces the amount of copper passing into the solution during the subsequent electrochemical study. The activity of platinum-copper catalysts in the MOR and the current-voltage characteristics of the H2/Air proton-exchange membrane fuel cell MEAs measured in the process of their life tests were much higher than those of the Pt/C catalysts. [ABSTRACT FROM AUTHOR]

A membrane electrolyte that restricts the methanol cross-over while retaining proton conductivity is essential for better electrochemical selectivity in direct methanol fuel cells (DMFCs). Extensive research carried out to explore numerous blends and composites for application as polymer electrolyte membranes (PEMs) revealed promising electrochemical selectivity in DMFCs of carbon nanomaterial-based polymer composites. The present review covers important literature on different carbon nanomaterial-based PEMs reported during the last decade. The review emphasises the proton conductivity and methanol permeability of nanocomposite membranes with carbon nanotubes, graphene oxide and fullerene as additives, assessing critically the impact of each type of filler on those properties. [ABSTRACT FROM AUTHOR]

This paper focuses on a literature analysis and review of sulfonated polymer (s-Poly) composites, sulfonated organic, inorganic, and organic–inorganic hybrid membranes for polymer electrolyte membrane fuel cell (PEM) systems, particularly for methanol fuel cell applications. In this review, we focused mainly on the detailed analysis of the distinct segment of s-Poly composites/organic–inorganic hybrid membranes, the relationship between composite/organic– inorganic materials, structure, and performance. The ion exchange membrane, their size distribution and interfacial adhesion between the s-Poly composites, nanofillers, and functionalized nanofillers are also discussed. The paper emphasizes the enhancement of the s-Poly composites/organic–inorganic hybrid membrane properties such as low electronic conductivity, high proton conductivity, high mechanical properties, thermal stability, and water uptake are evaluated and compared with commercially available Nafion® membrane. [ABSTRACT FROM AUTHOR]