Direct Methanol Fuel Cell Applications Research Articles

Pt Nanoparticles on Multi-Walled Carbon Nanotubes with High CO Tolerance for Methanol Electrooxidation

Anode catalysts are important for direct methanol fuel cells (DMFCs) of energy conversion. Herein, we report a novel strategy by ethylene glycol-based deep eutectic solvents (EG-DESs) for the fabrication of a multi-walled carbon nanotubes (MWCNTs)-supported Pt nanoparticles catalyst (referred to as Pt/CNTs-EG-DES). The Pt/CNTs-EG-DES catalyst provides an increased electrochemically active surface area (ECSA) and shows remarkably improved electrocatalytic performance towards methanol oxidation reaction compared to Pt/CNTs-W (fabricated in water) and commercial Pt/C catalysts. The improved performance is attributed to the generation of more Pt–O bonds which change the electronic states of the Pt atoms and the special node structure that obtains more active sites for a high CO resistance. This study suggests an effective synthesis strategy for Pt-based electrocatalysts with high performance for DMFC applications.

Recent Progresses and Challenges to Determine Properties of Sulfonated Polyether Ether Ketone Based Electrolytes for Direct Methanol Fuel Cell Applications

AbstractThis review focuses on fillers, modifications, and methods used in the preparation and development of sulfonated poly(ether ether ketone) (sPEEK) membranes, specifically for direct methanol fuel cell (DMFC) applications as proton exchange membranes in recent years. The primary objective is to evaluate recent advancements by emphasizing key characteristics such as water uptake and swelling capacity, ionic conductivity, methanol permeability, and single cell polarization tests. Additionally, the review aims to provide insights for future researchers by discussing the preparation processes of electrolytes. It presents basic characterizations of membrane electrolytes, including evaluations of the sulfonation degree and ion exchange capacities of sPEEK. High performance of membrane electrolytes is essential for commercialization and to compete with established membranes like Nafion®, which has a perfluorosulfonic acid structure. Therefore, the review also covers detailed characterization methods for assessing long‐term stability when available in the related studies. Numerical results and indicators are categorized and tabulated for easy interpretation and comparative analysis.

Ni- and Co-Based MOF-Derived NixCo3-xO4 Materials: As an Efficient Anode for Direct Methanol Fuel Cell Application.

Finding inexpensive and efficient anode materials is crucial for the oxidation of methanol in the direct methanol fuel cell (DMFC), which is the key electrode reaction. Herein, we report metal-organic framework (MOF)-derived Co3O4, NiO, and NixCo3-xO4 (where x = 1.5, 1, and 0.6) materials deposited on nickel foam as efficient anode material for methanol oxidation. Among them, NiCo2O4 exhibited the highest methanol oxidation activity, owing to its lowest charge-transfer resistance (0.097 Ω) and high electrochemically active surface area (1950 cm2), resulting in the lowest onset potential of 0.35 V vs Hg/HgO. The optimized Ni-to-Co ratio and synergistic effect between Ni and Co metals enable NiCo2O4 to achieve the highest mass activity of 151 mA mg-1 and geometric current density of 288 mA cm-2, demonstrating excellent durability over 14 h at 0.6 V. In addition, to optimize methanol concentration, all the electrocatalysts were tested in a range of methanol concentrations, showing 0.5 M methanol as the optimal concentration. This study focuses on optimizing the metal ratio and methanol concentration to achieve the highest catalytic activity. Additionally, this lays the foundation for developing diverse MOF-derived electrocatalysts and advancing DMFCs.

N-doped titanium oxide/carbon composite as supports for platinum catalysts in highly efficient methanol oxidation

The commercialization of direct methanol fuel cells (DMFCs) faces significant challenges due to the susceptibility of conventional platinum-based catalysts to poisoning by intermediates such as CO and HCOO− generated during the methanol oxidation reaction (MOR). This study details the synthesis of a highly porous titanium dioxide/carbon composite (TCC) using NH2-MIL-125(Ti) (MIL = Matérial Institut Lavoisier) as a precursor. To enhance the conductivity and catalytic properties of TCC, a nitriding reaction is conducted in an NH3 atmosphere, producing a nitrogen-doped titanium oxide/carbon composite (N-TCC). The resulting N-TCC is employed as a support for a platinum catalyst to improve MOR performance in DMFCs. The Pt/N-TCC catalyst demonstrates high catalytic performance, achieving a mass activity of 537 mA mg−1 for the MOR, marking a 39 % increase over the commercial Pt/C catalyst. Furthermore, the Pt/N-TCC catalyst exhibits a low onset potential for CO oxidation, a higher If/Ib ratio, and greater stability in chronoamperometry test, indicating high resistance to CO poisoning and enhanced chemical stability. Therefore, N-TCC can be used as a promising support for Pt-based catalysts in DMFC applications.

Harnessing the Potential of Hollow Graphitic Carbon Nanocages for Enhanced Methanol Oxidation Using PtRu Nanoparticles.

Direct Methanol Fuel Cell (DMFC) is a powerful system for generating electrical energy for various applications. However, there are several limitations that hinder the commercialization of DMFCs, such as the expense of platinum (Pt) at market price, sluggish methanol oxidation reaction (MOR) due to carbon monoxide (CO) formation, and slow electrooxidation kinetics. This work introduces carbon nanocages (CNCs) that were obtained through the pyrolysis of polypyrrole (Ppy) as the carbon source. The CNCs were characterized using BET, XRD, HRTEM, TEM, SEM, and FTIR techniques. The CNCs derived from the Ppy source, pyrolyzed at 750 °C, exhibited the best morphologies with a high specific surface area of 416 m2g-1, allowing for good metal dispersion. Subsequently, PtRu catalyst was doped onto the CNC-Ppy750 support using chemical reduction and microwave-assisted methods. In electrochemical tests, the PtRu/CNC-Ppy750 electrocatalyst demonstrated improved CO tolerance and higher performance in MOR compared to PtRu-supported commercial carbon black (CB), with values of 427 mA mg-1 and 248 mA mg-1, respectively. The superior MOR performance of PtRu/CNC-Ppy750 was attributed to its high surface area of CNC support, uniform dispersion of PtRu catalyst, and small PtRu nanoparticles on the CNC. In DMFC single-cell tests, the PtRu/CNC-Ppy750 exhibited higher performance, approximately 1.7 times higher than PtRu/CB. In conclusion, the PtRu/CNC-PPy750 represents a promising electrocatalyst candidate for MOR and anodic DMFC applications.

Tuning d-band center of Pt via Pt-Pt5La heterostructure interface as efficient and stable electrocatalyst for oxygen reduction and methanol oxidation reactions in DMFCs

Developing Pt-based electrocatalysts with superior activity and durability is essential for direct methanol fuel cells (DMFCs), and regulating the interfacial electronic interaction for Pt-based composites can significantly modulate the electrocatalytic performances. Herein, the Pt-Pt5La/C heterostructure catalyst was developed to enhance the catalytic property towards oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR). Experimental analyses and theoretical calculations demonstrated the electron redistribution at the interface and reduction of the d-band center of Pt for this unique Pt-Pt5La/C heterostructure. As the results, Pt-Pt5La/C exhibited 5.0- and 6.4-times higher mass activity and specific activity towards alkaline ORR compared to Pt/C, and the excellent electrocatalytic MOR performance due to the interfacial interaction. These superior electrocatalytic property promoted Pt-Pt5La/C as the bifunctional catalyst for DMFC application with outstanding power density and durability. Consequently, this work proposed a novel interfacial regulation strategy for designing Pt-rare earth (RE) alloy heterostructures and their reliable operation of DMFCs.

Performance Enhancement of Polymer Electrolyte Membrane with Nano-Calcium Carbonate Prepared by Mechanochemical for Direct Methanol Fuel Cell Applications

Performance Enhancement of Polymer Electrolyte Membrane with Nano-Calcium Carbonate Prepared by Mechanochemical for Direct Methanol Fuel Cell Applications

Static and dynamic properties investigation of modified polyethersulfone membrane for direct methanol fuel cell applications

The present study's main focus is understanding the impact of modification, especially through phosphoric acid and acetic acid, on polyethersulfone (PES) membranes for direct methanol fuel cell application, as sulfonation is the preferred modification method. The cross-linking introduces the sulfonate, phosphonate, and carboxylate group in the polymer matrix, while the membrane's semi-crystalline nature and homogeneous surface are confirmed through instrumental analysis. The high ion exchange capacity and water retention capacity of the phosphoric acid cross-linked PES membrane (PPES-2) reveal its potentiality. The impact of different hydration levels and temperatures on proton conductivity indicates that based on the operating conditions, the cross-linked membrane can be used, such as at high temperatures and 50 % hydration level, the PPES-2 membrane shows high proton conductivity as well as has low methanol crossover due to the presence of hydroxyl group. At the same time, the acetic acid-treated PES (CPES-2) membrane shows high proton conductivity at 50 % hydration level and low temperature. The same is confirmed through molecular dynamic simulation by understanding their dynamic and static properties. The PPES-2 membrane shows maximum power density (0.34 Wcm−2). In conclusion, the study indicates that PES modification can be done through phosphorylation and carboxylation, apart from sulfonation.

Chitosan/magnetic chitin nanowhisker polyelectrolyte membrane for direct methanol fuel cell applications: preparation, characterization, and performance analysis

ABSTRACT A hybrid chitosan-based nanocomposite was fabricated by chitin nanowhiskers coupled with silanized Fe3O4 nanoparticles as a polyelectrolyte membrane for direct methanol fuel cells (DMFCs). The morphological evaluations articulated that the magnetite nanoparticles were uniformly attached to the chitin nanowhiskers. After characterization of the synthesized nanowhiskers, they were incorporated into the chitosan, as a polycationic electrolyte, to investigate the performance of nanocomposite for DMFC applications. An external magnetic field was applied to the magnetic chitin nanowhiskers to induce alignment, and the effects of aligned nanowhiskers, as well as random ones, were also studied. The magnetic chitin nanowhiskers positively influenced the water uptake and proton conductivity due to the formation of hydrogen bonds between the surface functional groups of nanowhiskers and free water molecules. On the other hand, methanol permeation of the chitosan nanocomposites was reduced regarding the tortuous pathways and narrower transportation channels by the presence of nanowhiskers.

Nickel-modified poly(aniline-co-pyrrole) as electrocatalyst for electrochemical oxidation of methanol in direct methanol fuel cell application

Nickel-modified poly(aniline-co-pyrrole) as electrocatalyst for electrochemical oxidation of methanol in direct methanol fuel cell application

Development of novel proton exchange membranes based on cross-linked polyvinyl alcohol (PVA)/5-sulfosalicylic acid (SSCA) for fuel cell applications

The proton-conducting and methanol permeation behaviors of polymeric electrolyte membranes (PEMs), as well as the expensive nature of direct methanol fuel cell (DMFC) components, pose major concerns in DMFC performance and commercialization. As a result, this research aimed to develop low-cost polyelectrolyte membranes based on cross-linked poly(vinyl alcohol)/5-sulfosalicylic acid dehydrate (PVA/SSCA) composite. Chemical cross-linkers and modifiers offer the essential chemical and mechanical stability of the developed membranes for usage as polyelectrolyte membranes (PEMs). The manufactured composite proton exchange membranes provide several benefits, including significant thermal, chemical, and mechanical stability. The results revealed that extending the SSCA molar concentration increased IEC outcomes of the synthesized membranes, reaching an elevated level of (3.31 meq g−1) compared to (0.91 meq g−1) for the Nafion 117 membrane. The proton conductivity of a composite membrane (102 μm thick) measured by impedance spectroscopy was relatively (0.078 S cm−1) and found comparable to other PVA-based composite membranes reported in the literature. Other key parameters, such as methanol permeability, were measured for constructed composite proton exchange membranes (2.52 × 10–7 cm2 s−1), which were much lower than Nafion 117 (3.39 × 10–6 cm2 s−1). The Fourier transform infrared (FT-IR), Raman scattering spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, elemental analysis, and thermal gravimetric analysis (TGA) were among the techniques used to characterize the synthesized membranes. These characterizations confirm the structural interaction between the membrane components’ crystalline nature, and no signs of phase separation or cracks were found; surface morphology and good membrane homogeneity, elemental analysis, and the membranes’ thermal stability (up to 290 °C). The membranes were also mechanically characterized using a universal testing machine (UTM), which revealed good mechanical stability. The findings demonstrate that a low-cost proton exchange membrane could potentially be synthesized for DMFC applications.

New type nanocomposite based on metal-organic frameworks decorated with nickel nanoparticles as a potent electrocatalyst for methanol oxidation in alkaline media

Methanol oxidation reaction (MOR) is used to provide electrical energy via direct methanol fuel cell (DMFC), which requires a practical design of electrocatalysts to accelerate the sluggish MOR. In this study, we successfully fabricated the carbon black nanoparticles/graphite ceramic electrode (CBNPs/GCE) supported metal-organic frameworks (MOFs) and decorated with nickel nanoparticles (NiNPs) as a new type nanocomposite modified electrode (NiNPs/MOFs/CBNPs/GCE) via a chemical and an electrochemical process, respectively. The surface morphology and structure of the synthesized nanocomposite materials and modified electrodes were characterized using field emission scanning electron microscopy, energy dispersive X-ray analysis, Fourier transform infrared spectroscopy, X-ray diffraction and thermogravimetric analysis. Then, the NiNPs/MOFs/CBNPs/GCE was used as a non-platinum electrocatalyst for electrocatalytic oxidation of methanol in alkaline media. The obtained results show the efficient electrocatalytic activity of the NiNPs/MOFs/CBNPs/GCE toward the MOR with high anodic peak current density (Jpa = 34.8 mA cm−2) compared with the other prepared electrocatalysts; MOFs/CCE, NiNPs/CCE, MOFs/CBNPs/GCE, NiNPs/CBNPs/GCE, and NiNPs/MOFs/CCE, due to the synergistic effect of nanocomposite components; NiNPs, MOFs and CBNPs. The prepared electrocatalyst; NiNPs/MOFs/CBNPs/GCE, not only shows a high electrochemically active surface area (ECSA = 2.15 cm2) but also has long-term durability in MOR. In general, it can be said the NiNPs/MOFs/CBNPs/GCE is a promising candidate for application in DMFC.

Self-healing sulfonated poly(ether ether ketone)/polyvinyl alcohol membrane reinforced with sulfonated silica for direct methanol fuel cell

Nafion, the predominant choice for polymer electrolyte membranes (PEMs) in direct methanol fuel cells (DMFCs), excels in proton conductivity but is plagued by elevated methanol permeability and sustained performance degradation. To address these issues, this study aims to synthesize a self-healable composite membrane composed of sulfonated poly (ether ether ketone), polyvinyl alcohol, and sulfonated silica (S/PVA/S–SiO2). The composite membrane with 3 wt% S–SiO2 demonstrates the highest proton conductivity, thanks to its improved water absorption and increased proton transfer sites. Compared to pure SPEEK, the composite membrane has a 20% lower methanol permeability. With its enhanced selectivity, the S/PVA/S–SiO2 membrane produces a power density of 3.64 mW cm−2 at 26.67 mA cm−2. Furthermore, by virtue of reversible hydrogen bonding, the composite membrane shows exceptional self-healing capabilities, restoring its methanol-blocking function by 83.6%. These results highlight that the S/PVA/S–SiO2 membrane holds promise for DMFC applications.

The Size and Charge Effect of Pt Cluster on the Electrocatalytic Activity Toward the First Step of Dehydrogenation of Methanol

Abstract The O–H/C–H scission of methanol on Pt clusters is a crucial step in direct methanol fuel cells applications. The first dehydrogenation process of methanol on Ptnq clusters (n = 5, 13, 19; q = 0, +1, −1) in various charge states is studied. Our findings indicate that methanol adsorbs more easily on cationic Ptn+ than on neutral Ptn or anionic Ptn−. However, the adsorption capacity of methanol on Ptnq gradually decreases with increasing cluster size, especially for CH3OH on Ptn+, which decreases significantly (from −57.61 kcal/mol to −16.41 kcal/mol). Compared with Ptn and Ptn+, the energy barrier of O–H/C–H bond cleavage is significantly reduced by injecting an electron into Ptn to form Ptn−, and the activity of the catalyst is improved. However, the energy barrier of O–H/C–H cleavage increases gradually with cluster size, leading to a decrease in catalytic activity. The effect of charge weakens as cluster size increases, and small clusters with injected electrons exhibit better catalytic activity.

Green and sustainable use of macadamia nuts as support material in Pt-based direct methanol fuel cells

The successful commercialization of direct methanol fuel cells (DMFCs) is hindered by inadequate methanol oxidation activity and anode catalyst longevity. Efficient and cost-effective electrode materials are imperative in the widespread use of DMFCs. While Platinum (Pt) remains the primary component of anodic methanol oxidation reaction (MOR) electrocatalysts, its utilization alone in DMFC systems is limited due to carbon monoxide (CO) poisoning, instability, methanol crossover, and high cost. These limitations impede the economic feasibility of Pt as an electrocatalyst. Herein, we present the use of powdered activated carbon (PAC) and granular activated carbon (GAC), both sourced from macadamia nut shells (MNS), a type of biomass. These bio-based carbon materials are integrated into hybrid supports with reduced graphene oxide (rGO), aiming to enhance the performance and reduce the production cost of the Pt electrocatalyst. Electrochemical and physicochemical characterizations of the synthesized catalysts, including Pt-rGO/PAC-1:1, Pt-rGO/PAC-1:2, Pt-rGO/GAC-1:1, and Pt-rGO/GAC-1:2, were conducted. X-ray diffraction analysis revealed crystallite sizes ranging from 1.18 nm to 1.68 nm. High-resolution transmission electron microscopy (HRTEM) images with average particle sizes ranging from 1.91 nm to 2.72 nm demonstrated spherical dispersion of Pt nanoparticles with some agglomeration across all catalysts. The electrochemical active surface area (ECSA) was determined, with Pt-rGO/GAC-1:1 exhibiting the highest ECSA of 73.53 m2 g−1. Despite its high ECSA, Pt-rGO/GAC-1:1 displayed the lowest methanol oxidation reaction (MOR) current density, indicating active sites with poor catalytic efficiency. Pt-rGO/PAC-1:1 and Pt-rGO/PAC-1:2 exhibited the highest MOR current densities of 0.77 mA*cm−2 and 0.74 mA*cm−2, respectively. Moreover, Pt-rGO/PAC-1:2 and Pt-rGO/PAC-1:1 demonstrated superior electrocatalytic mass (specific) activities of 7.55 mA/mg (0.025 mA*cm−2) and 7.25 mA/mg (0.021 mA*cm−2), respectively. Chronoamperometry tests revealed Pt-rGO/PAC-1:2 and Pt-rGO/PAC-1:1 as the most stable catalysts. Additionally, they exhibited the lowest charge transfer resistances and highest MOR current densities after durability tests, highlighting their potential for DMFC applications. The synthesized Pt supported on PACs hybrids demonstrated remarkable catalytic performance, stability, and CO tolerance, highlighting their potential for enhancing DMFC efficiency.

Proton exchange membranes based on sulfonated polybutylene fumarate: Preparation and characterization

AbstractBased on a novel unsaturated polyester, polybutylene fumarate (PBF), a series of sulfonated proton exchange membranes were prepared and characterized for direct methanol fuel cell application. In this work, PBF underwent sulfonation at different degrees, and the optimum degree of sulfonation (DS) was identified by assessing the hydrolytic stability. In the second step, an effective strategy to enhance the membranes' proton conductivity was adopted by the addition of the 2‐(1H‐Imidazol‐2‐yl) acetic acid (Im‐COOH) compound as a proton‐conducting agent to the sulfonated PBF (SPBF) matrix with the optimum DS. The results unveiled significant alterations in the physicochemical properties of PBF due to sulfonation, including an elevation in water uptake and the glass transition temperature (Tg), accompanied by the disappearance of the crystallinity within SPBF. In terms of electrochemical characteristics, the SPBF‐17.5 PEM demonstrated a proton conductivity of 3.36 × 10−3 S cm−1 and a methanol permeability of 1.068 × 10−7 cm2 s−1, yielding a selectivity of approximately 31,460 S s cm−3. Furthermore, the attractive interactions between SO3H and NH groups further elevated proton conductivity to 4.12 × 10−3 S cm−1, accompanied by a decrease in methanol permeability to 0.942 × 10−7 cm2 s−1, enhancing the selectivity parameter to 43,736 S s cm−3.

Lutetium-Induced Ultrafine PtRu Nanoclusters with a High Electrochemical Surface Area for Direct Methanol Fuel Cells at Alleviated Temperatures.

PtRu alloys have been recognized as the state-of-the-art catalysts for the methanol oxidation reaction (MOR) in direct methanol fuel cells (DMFCs). However, their applications in DMFCs are still less efficient in terms of both catalytic activity and durability. Rare earth (RE) metals have been recognized as attractive elements to tune the catalytic activity, while it is still a world-class challenge to synthesize well-dispersed Pt-RE alloys. Herein, we developed a novel hydrogen-assisted magnesiothermic reduction strategy to prepare a highly dispersed carbon-supported lutetium-doped PtRu catalyst with ultrafine nanoclusters and atomically dispersed Ru sites. The PtRuLu catalyst shows an outstanding high electrochemical surface area (ECSA) of 239.0 m2 gPt-1 and delivers an optimized MOR mass activity and specific activity of 632.5 mA mgPt-1 and 26 A cmPt-2 at 0.4 V vs saturated calomel electrode (SCE), which are 3.6 and 3.5 times of commercial PtRu-JM and an order higher than PtLu, respectively. These novel catalysts have been demonstrated in a high-temperature direct methanol fuel cell running in a temperature range of 180-240 °C, achieving a maximum power density of 314.3 mW cm-2. The AC-STEM imaging, in situ ATR-IR spectroscopy, and DFT calculations disclose that the high performance is resulted from the highly dispersed PtRuLu nanoclusters and the synergistic effect of the atomically dispersed Ru sites with PtRuLu nanoclusters, which significantly reduces the CO* intermediates coverage due to the promoted water activation to form the OH* to facilitate the CO* removal.

Chitosan Incorporated with Titanium (IV) Oxide Membrane for Direct Methanol Fuel Cell Application

The direct methanol fuel cell (DMFC), a type of promoted polymer electrolyte membrane fuel cell (PEMFC), has received tremendous attention in the past two decades because of its potential as a promising technology for clean and efficient power generation in the twenty-first century. Over the past four decades, the dominancy of perfluorinated proton exchange membranes (PEM) such as Nafion is prolonging in the current PEM technology due to its chemical stability, high proton conductivity and high mechanical strength in the low operating temperatures. However, the Nafion membrane also has several weaknesses, such as high methanol permeability, high manufacturing cost, and dehydration with low proton conductivity at elevated temperatures > 100°C. This study fabricated a novel composite membrane by blending the pristine chitosan (CS) and titanium oxide (TiO2) at various loadings, 0.5, 1.0, 1.5 and 2.0 wt% to obtain high performance in DMFC. SEM and FTIR analysis showed that the grafting of (O-Ti-O) successfully incorporated into the CS polymer matrix. Water and methanol uptake of CS/TiO2 composite membrane decreased with increase of TiO2 loadings, but proton conductivity value increased. The CS/TiO2 membrane with 1.5wt.%TiO2 loading exhibited highest proton conductivity (0.41mScm-1) and lowest methanol permeability (17.18E-08cm2/s) characteristics among other membranes this due to the hydrophilic TiO2 raised the membrane hydrophilic character by increasing the number of hydrophilic sites, such as OH-, COO- and O-. The results obtained from the study can be used to conclude that chitosan membrane with TiO2 filler is a promising high performance PEM candidate for DMFC applications.

Effects of heated-treating temperature on the stability and electrochemical performance of alginate-based multi-crosslinked biomembranes

In this study, the organosilane nanoparticles as additive and crosslinker were prepared and incorporated into sodium alginate to fabricate a series of alginate-based multi-crosslinked biomembranes at different thermal treatment temperature without the usage of another crosslinking agent. The effects of treatment temperature on the stability of biomembranes including dimensional, oxidative, hydrolytic and mechanical stability were investigated in detail. As a whole, the stability of biomembranes exhibited increasing tendency with the increment of treatment temperature due to the formation of more compact internal network structure. The electrochemical performance of biomembranes in respect to their potential as proton exchange membranes for direct methanol fuel cell application were also investigated based on the treatment temperature. The results revealed that the biomembranes possessed excellent methanol resistance and the methanol diffusion coefficient decreased with the increment of treatment temperature. The biomembrane with 120 °C heat-treatment showed the optimal selectivity (14.30 × 105 Ss cm−3), which was about 1.77 and 68.10 times of that and of M-80 (8.09 × 105 Ss cm−3) and Nafion@117 (0.21 × 105 Ss cm−3), respectively. Fuel cell performance measurements showed that M-120 possessed higher maximum power density and cell stability compared with M-80 and Nafion@117, indicating its best adaptability for use in direct methanol fuel cell.

Dual role of 2-aminodiphenylamine with graphene oxide-palladium supported catalyst for direct methanol fuel cell application and removal of Otto fuel II component

For the first time, we describe the synthesis of Pd nanoparticles (Pd(0)) using 2-aminodiphenylamine (2ADPA) with graphene oxide as support. Furthermore, we incorporated the Pd(0)-2ADPA, which was enriched with graphene oxide and used to modify a glassy carbon electrode surface. We used this catalyst as the methanol oxidation reaction (MOR) in the alkaline media shows good catalytic behavior within the fuel cell application and removal of the Otto fuel II component. Several characterizations evidence the successful formation of Pd(0)-2ADPA by spectroscopic and optical techniques. We have studied the reduction reaction of the 2-nitrodiphenylamine (2-NDPA) to investigate the catalytic performance of the synthesized material. We used various electrochemical methods, for example, chronoamperometry (CA) and cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), to review the stability of our proposed catalyst. The stability of the Pd electrocatalyst was improved by covering it with 2ADPA. The incorporated Pt-free electrocatalyst is incredibly favorable for facilitating the direct methanol fuel cell cost due to the incorporation of conductive polymer support material.