Search Results (39)

One of the key challenges in commercializing proton exchange membrane (PEM) electrolyzer technology is reducing the production costs while maintaining high efficiency and operational stability. Significant contributors to the overall cost of the device are the electrode catalysts with IrO₂ and Pt/C. Due to the high cost and limited availability of noble metals, there is growing interest in developing alternative, low-cost catalytic materials. In recent years, two-dimensional transition metal dichalcogenides (2D TMDCs), such as molybdenum disulfide (MoS₂) and rhenium disulfide (ReS₂), have attracted considerable attention due to their promising electrochemical properties for hydrogen evolution reactions (HERs). These materials exhibit unique properties, such as a high surface area or catalytic activity localized at the edges of the layered structure, which can be further enhanced through defect engineering or phase modulation. To increase the catalytically active surface area, the investigated materials were deposited on a carbon-based support—Vulcan XC-72R—selected for its high electrical conductivity and large specific surface area. This study investigated the physicochemical and electrochemical properties of six catalyst samples with varying MoS₂ and ReS₂ to carbon support ratios. Among the composites analyzed, the best sample on MoS₂ (containing the most carbon soot) and the best sample on ReS₂ (containing the least carbon soot) were selected. These were then used as cathode catalysts in an experimental PEM electrolyzer setup. The results confirmed satisfactory catalytic activity of the tested materials, indicating their potential as alternatives to conventional noble metal-based catalysts and providing a foundation for further research in this area. Full article

The anodic stability of tungsten carbide (WC) and iron oxide with a spinel structure (Fe₃O₄) were compared against similar data for nanostructured, boron-doped diamond (BDD), and the benchmark Vulcan XC72 carbon, in view of their eventual application as alternative supports for the anion exchange membrane electrolyzer anode. To this end, metal oxide composites were prepared by the in situ autocombustion (ISAC) method, and the anodic behavior of materials (composites as well as supports alone) was investigated in 1 M NaOH electrolyte by the rotating ring–disc electrode method, which enables the separation oxygen evolution reaction and materials’ degradation currents. Among all supports, BDD has proven to be the most stable, while Vulcan XC72 is the least stable under the anodic polarization, with Fe₃O₄ and WC demonstrating intermediate behavior. The Co₃O₄-BDD, -Fe₃O₄, -WC, and -Vulcan composites prepared by the ISAC method were then tested as catalysts of the oxygen evolution reaction. The Co₃O₄-BDD and Co₃O₄-Fe₃O₄ composites appear to be competitive electrocatalysts for the OER in alkaline medium, showing activity comparable to the literature and higher support stability towards oxidation, either in cyclic voltammetry or chronoamperometry stability tests. On the contrary, WC- and Vulcan-based composites are prone to degradation. Full article

This work reports the synthesis of PdNi bimetallic particles and Pd on Carbon black (Vulcan XC-72) by reverse microemulsion and the chemical reduction of metallic complexes. The physicochemical characterization techniques used for the bimetallic and metallic materials were TGA, STEM, ICP-OES, and XRD. Also, the electrocatalysts were studied by electrochemical techniques such as anodic CO stripping and β-NiOOH reduction to elucidate the Pd and Ni surface sites participation in the reactions. The electrocatalysts were evaluated in the anodic reaction in anion-exchange membrane fuel cells (AEMFC) and the hydrogen oxidation reaction (HOR) in alkaline media. The results indicate that PdNi/C electrocatalysts exhibited higher electrocatalytic activity than Pd/C electrocatalysts in both the half-cell test and in the AEMFC, even with the same Pd loading, which is attributed to the bifunctional mechanism that provides OH^- groups in oxophilic sites associated to Ni, that can facilitate the desorption of Hads in the Pd sites for the bimetallic material. Full article

This work aims at the effects of anion-exchange membranes (AEMs) and ionomer binders on the catalyst electrodes for anion-exchange membrane fuel cells (AEMFCs). In the experiments, four metal catalysts (nano-grade Pt, PtRu, PdNi and Ag), four AEMs (aQAPS-S8, AT-1, X37-50T and X37-50RT) and two alkaline ionomers (aQAPS-S14 and XB-7) were used. They were verified through several technical parameters examination and cell performance comparison for the optimal selection of AMEs. The bimetallic PdNi nanoparticles (PdNi/C) loaded with Vulcan XC-72R carbon black were used as anode electrodes by using the wet impregnation method, and Ag nanoparticles (Ag/C) were used as the catalyst cathode. It was found that the power density and current density of the X37-50RT are higher than the other three membranes. Also, alkaline ionomers of XB-7 had better performance than aQAPS-S14. The efficiency was improved by 32%, 155% and 27%, respectively, when compared to other membranes by using the same catalyst of PdNi/C, Ag/C and Pt/C. The results are consistent with the membrane ion conductivity measurements, which showed that the conductivity of the X37-50RT membrane is the highest among them. The conductivity values for hydroxide ions (OH⁻) and bromide ions (Br⁻) are 131 mS/cm and 91 mS/cm, respectively. These findings suggest that the properties (water uptake, swelling rate and mechanical) of the anion-exchange membrane (AEM) can serve as a key reference for AEM fuel cell applications. Full article

Aqueous phase reforming (APR) is a promising method for producing hydrogen from biomass-derived feedstocks. In this study, carbon-supported Pt catalysts containing particles of different sizes (below 3 nm) were deposited on different commercially available carbons (i.e., Vulcan XC72 and Ketjenblack EC-600JD) using the metal vapor synthesis approach, and their catalytic efficiency and stability were evaluated in the aqueous phase reforming of ethylene glycol, the simplest polyol containing both C–C and C–O bonds. High-surface-area carbon supports were found to stabilize Pt nanoparticles with a mean diameter of 1.5 nm, preventing metal sintering. In contrast, Pt single atoms and clusters (below 0.5 nm) were not stable under the reaction conditions, contributing minimally to catalytic activity and promoting particle growth. The most effective catalyst Pt_A/C^K, containing a mean Pt NP size of 1.5 nm and highly dispersed on Ketjenblack carbon, demonstrated high hydrogen site time yield (8.92 min⁻¹ at 220 °C) and high stability under both high-temperature treatment conditions and over several recycling runs. The catalyst was also successfully applied to the APR of polyethylene terephthalate (PET), showing potential for hydrogen production from plastic waste. Full article

This research focuses on the rational design of porous enzymatic electrodes, using horseradish peroxidase (HRP) as a model biocatalyst. Our goal was to identify the main obstacles to maximizing biocatalyst utilization within complex porous structures and to assess the impact of various carbon nanomaterials on electrode performance. We evaluated as-synthesized carbon nanomaterials, such as Carbon Aerogel, Coral Carbon, and Carbon Hollow Spheres, against the commercially available Vulcan XC72 carbon nanomaterial. The 3D electrodes were constructed using gelatin as a binder, which was cross-linked with glutaraldehyde. The bioelectrodes were characterized electrochemically in the absence and presence of 3 mM of hydrogen peroxide. The capacitive behavior observed was in accordance with the BET surface area of the materials under study. The catalytic activity towards hydrogen peroxide reduction was partially linked to the capacitive behavior trend in the absence of hydrogen peroxide. Notably, the Coral Carbon electrode demonstrated large capacitive currents but low catalytic currents, an exception to the observed trend. Microscopic analysis of the electrodes indicated suboptimal gelatin distribution in the Coral Carbon electrode. This study also highlighted the challenges in transferring the preparation procedure from one carbon nanomaterial to another, emphasizing the importance of binder quantity, which appears to depend on particle size and quantity and warrants further studies. Under conditions of the present study, Vulcan XC72 with a catalytic current of ca. 300 µA cm⁻² in the presence of 3 mM of hydrogen peroxide was found to be the most optimal biocatalyst support. Full article

This work reports the influence of a reduced graphene oxide (rGO) support on the catalytic performance of Cu@PtRu/rGO electrocatalysts toward methanol oxidation in an acidic medium. These electrocatalysts are synthesized via a two-step reduction method; the first step utilizes ethylene glycol for the reduction of Cu²⁺ ions, forming Cu/rGO. In the second step, spontaneous redox reactions take place, in a process known as galvanic displacement, where the Pt²⁺ and Ru³⁺ species are reduced to form PtRu layers, and the copper is partially oxidized to the solution. Then, the Cu@PtRu/rGO core–shell is produced, comprising Cu in the inner structure (core) and PtRu on the outer part (shell). To compare the catalytic performance of the prepared nanocatalysts (NCs), Pt/C, PtRu/C, and Cu@PtRu/C are also synthesized on Vulcan XC-72R carbon. All catalysts are characterized via X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Cyclic voltammetry (CV) and chronoamperometry (CA) are employed to measure the electrochemical performance. The core–shell/rGO combination is superior in catalytic activity to the traditional Pt/C, PtRu/C, and Cu@PtRu/C catalysts for the methanol oxidation reaction. These results suggest that Cu@PtRu/rGO exhibits a high bulk activity for methanol electrooxidation, a high stability, and a high tolerance to CO poisoning, meaning it is possible to reduce the platinum loading in proton-exchange membrane fuel cells (PEMFCs). Full article

The through-plane gas permeability and morphology of PEFC gas diffusion media (GDM) is investigated for different microporous layer (MPL) ink homogenisation techniques (bath sonication and magnetic stirring) for low- (Vulcan XC-72R) and high (Ketjenblack EC-300J)-surface-area carbon powders. The MPL composition is held constant at 80 wt.% carbon powder and 20 wt.% PTFE for a carbon loading of 1.0 mg cm⁻². The MPL ink homogenisation time is held constant at two hours for both techniques and increased by one hour for bath sonication to compare with previous investigations. The results show that the through-plane gas permeability of the GDM is approximately doubled using magnetic stirring when compared with bath sonication for MPLs composed of Vulcan XC-72R, with a negligible change in surface morphology between the structures produced from either homogenisation technique. The variation in through-plane gas permeability is almost negligible for MPLs composed of Ketjenblack EC-300J compared with Vulcan XC-72R; however, MPL surface morphology changes considerably with bath sonication, producing smoother, less cracked surfaces compared to the large cracks produced via magnetic stirring for a large-surface-area carbon powder. An MPL ink sonication time of three hours results in a percentage reduction in through-plane gas permeability from the GDL substrate permeability by ~72% for Ketjenblack EC-300J compared to ~47% for two hours. Full article

The present work reports the synthesis and the physicochemical characterization of biochar from the organic wastes of nopal (Opuntia Leucotricha), coffee grounds (Coffea arabica) and Ataulfo mango seeds (Mangifera indica) as alternative electrocatalyst supports to Vulcan XC-72 carbon black. The biochars were prepared using pyrolysis from organic wastes collected at three temperatures, 600, 750 and 900 °C, under two atmospheres, N₂ and H₂. The synthesized biochars were characterized using Raman spectroscopy and scanning electron microscopy (SEM) to obtain insights into their chemical structure and morphological nature, respectively, as a function of temperature and pyrolysis atmosphere. A N₂ adsorption/desorption technique, two-point conductivity measurements and cyclic voltammetry (CV) were conducted to evaluate the specific surface area (SSA), electrical conductivity and double-layer capacitance, respectively, of all the biochars to estimate their physical properties as a possible alternative carbon support. The results indicated that the mango biochar demonstrated the highest properties among all the biochars, such as an electrical conductivity of 8.3 S/cm⁻¹ at 900 °C in N₂, a specific surface area of 829 m²/g at 600 °C in H₂ and a capacitance of ~300 mF/g at 900 °C in N₂. The nopal and coffee biochars exhibited excellent specific surface areas, up to 767 m²/g at 600 °C in N₂ and 699 m²/g at 750 °C in H₂, respectively; nonetheless, their electrical conductivity and capacitance were limited. Therefore, the mango biochar at 900 °C in N₂ was considered a suitable alternative carbon material for electrocatalyst support. Additionally, it was possible to determine that the electrical conductivity and capacitance increased as a function of the pyrolysis temperature, while the specific surface area decreased for some biochars as the pyrolysis temperature increased. Overall, it is possible to conclude that heat treatment at a high temperature of 900 °C enhanced the biochar properties toward electrocatalyst support applications. Full article

The adsorption of phenol (Ph), 4-chlorophenol (CP), and 4-cresol (MP) from aqueous solutions on three carbonaceous materials of diverse origins but similar specific surface areas was investigated. Vulcan XC72 carbon black (CB), AKP-5 activated coke (AC), and activated tire pyrolysis char (AP) were examined as adsorbents. The kinetics and equilibrium adsorption, as well as the influence of pH and ionic strength of each solution on the adsorption process, were studied. The results revealed that the adsorption was pH-dependent and preferred an acidic environment. The presence of an inorganic salt in the solution (ionic strength) did not affect the adsorption processes of the three adsorbates. The pseudo-first- and pseudo-second-order equations, as well as the Weber–Morris and Boyd kinetic models, were used to describe the adsorption kinetics. It was found that equilibrium was reached for all adsorbates after approximately 2–3 h. Adsorption kinetics followed a pseudo-second-order model, and the adsorption rate was determined by film diffusion. The adsorption isotherms were described using the Langmuir and Freundlich equations. The results revealed that the adsorption processes of Ph, CP, and MP on all three adsorbents from the water were better described by the Langmuir model. The adsorption of CP was the most efficient, the adsorption of MP was slightly weaker, and the adsorption of phenol was the least efficient. Full article

This work highlights the potential for the synthesis of new PtSnZn catalysts with enhanced efficiency and durability for methanol oxidation reaction (MOR) in low-temperature fuel cells. In this research, PtZn and PtSnZn nanoparticles deposited on high surface area Vulcan XC-72R Carbon support were created by a microwave-assisted polyol method. The electrochemical performances of synthesized catalysts were analyzed by cyclic voltammetry and by the electrooxidation of adsorbed CO and the chronoamperometric method. The physicochemical properties of obtained catalysts were characterized by transmission electron microscopy (TEM), thermogravimetric (TGA) analysis, energy dispersive spectroscopy (EDS) and by X-ray diffraction (XRD). The obtained findings showed the successful synthesis of platinum-based catalysts. It was established that PtSnZn/C and PtZn/C catalysts have high electrocatalytic performance in methanol oxidation reactions. Catalysts stability tests were obtained by chronoamperometry. Stability tests also confirmed decreased poisoning and indicated improved stability and better tolerance to CO-like intermediate species. According to activity and stability measurements, the PtSnZn/C catalyst possesses the best electrochemical properties for the methanol oxidation reaction. The observed great electrocatalytic activity in the methanol oxidation reaction of synthesized catalysts can be attributed to the beneficial effects of microwave synthesis and the well-balanced addition of alloying metals in PtSnZn/C catalysts. Full article

Herein, a straightforward electrochemical method was used to evaluate the total phenolic antioxidant capacity in natural extracts prepared from pomegranate, hibiscus, and pitaya. In light of this, the well-known electrochemical index (EI), a screening protocol for natural antioxidant properties evaluation, was determined using differential pulse voltammetry. Initially considering rutin and catechin as standards, we found that the system’s sensitivity greatly increased by using platinum (Pt) and platinum/ruthenium (Pt/Ru) nanoparticles (NPs) immobilized on Vulcan XC-72 to modify screen-printed carbon electrodes (SPCEs). When such modifications were applied to natural fruit/plant extracts, their electrochemical ability proved highly superior to the bare SPCE, even considering a very small amount of materials for electrode preparation. However, with an optimized ratio, the bimetallic counterpart was more sensitive to detection. When the pomegranate extract was used, for example, EI values of 52.51 ± 6.00 and 104.79 ± 6.89 µA/V were obtained using Pt and Pt/Ru (with an optimized ratio) electrocatalysts, showing the remarkable sensitivity increase obtained in our bimetallic protocol. Thus, based on physicochemical and electrochemical characterizations, we found that the ruthenium content was essential for the achievements. In due course, XPS analysis suggested that the Pt²⁺/Pt⁰ species ratio could have improved the system’s sensitivity, which significantly changed when ruthenium was used in the material. Full article

In the present work, the chemical synthesis of AgPt nanoalloys is reported by the polyol method using polyvinylpyrrolidone (PVP) as a surfactant and a heterogeneous nucleation approach. Nanoparticles with different atomic compositions of the Ag and Pt elements (1:1 and 1:3) were synthesized by adjusting the molar ratios of the precursors. The physicochemical and microstructural characterization was initially performed using the UV-Vis technique to determine the presence of nanoparticles in suspension. Then, the morphology, size, and atomic structure were determined using XRD, SEM, and HAADF-STEM techniques, confirming the formation of a well-defined crystalline structure and homogeneous nanoalloy with an average particle size of less than 10 nm. Finally, the cyclic voltammetry technique evaluated the electrochemical activity of bimetallic AgPt nanoparticles supported on Vulcan XC-72 carbon for the ethanol oxidation reaction in an alkaline medium. Chronoamperometry and accelerated electrochemical degradation tests were performed to determine their stability and long-term durability. The synthesized AgPt (1:3)/C electrocatalyst presented significative catalytic activity and superior durability due to the introduction of Ag that weakens the chemisorption of the carbonaceous species. Thus, it could be an attractive candidate for cost-effective ethanol oxidation compared to commercial Pt/C. Full article

The durability of low temperature proton exchange membrane fuel cell (PEMFC) catalysts crucially affects their lifetime. The choice of carbon support is important in terms of increasing the stability of catalysts. In this research, Pt/C samples were obtained using the polyol synthesis method on two types of carbon supports: the standard support, Vulcan XC-72, and carbon support with a high degree of graphitization, ECS-002402. One method for assessing structural characteristics is through transmission electron microscopy (TEM), according to which materials G1 and G2 showed an average nanoparticle size of 3.7 and 4.2 nm, respectively. On all catalysts, the oxygen reduction reaction proceeded according to the four electron mechanism. Durability was assessed by changes in ESA and activity in the ORR after 1000 cycles, with changes in the upper potential values: 0.7; 1.0; 1.2; and 1.4 V. After accelerated stress testing, the G1 material showed the greatest residual activity at a potential of 1.4 V (165 A/g (Pt). Based on the results of comparing various ADT protocols, the optimal mode of 0.4 and 1.4 V was chosen, and should be used for further studies comparing the durability of Pt/C catalysts. Full article

A high methanol electro-oxidation (MOR) and carbon monoxide (CO) tolerance satisfied the electrochemical requirements of direct methanol fuel cells (DMFCs). The study investigated strontium molybdate (SrMoO₄) mixed with Vulcan XC-72, carbon-loaded with 20% Pt. The electrochemical performance was confirmed by MOR and CO tolerance activities measured via cyclic voltammetry (CV). The synergistic effect between Pt and SrMoO₄ is essential to affect the electrochemical characteristic. SrMoO₄ can help remove CO-like intermediate products on the Pt surface, enhancing electrochemical performance for DMFCs. In addition, H_xMoO₃/H_yMoO₃ existence in Sr_0.5Mo_0.5O_4−δ can quickly remove intermediates from Pt surfaces and accelerate the transformation of adsorbed intermediates to CO₂. The results obtained showed that 20%-Pt/uncalcined Sr_0.5Mo_0.5O_4−δ-C electrocatalyst has higher MOR and CO tolerance ability in DMFCs. Furthermore, the fabricated DMFC shows excellent long-term electrochemical stability after 1000 cycles and a maximum power density (1.42 mW/cm²) higher than commercial 20%-Pt/C (1.27 mW/cm²). Full article