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Keywords = direct ethanol fuel cell

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15 pages, 3692 KiB  
Article
Empirical Comparison of Flow Field Designs for Direct Ethanol-Based, High-Temperature PEM Fuel Cells
by Prantik Roy Chowdhury and Adam C. Gladen
Fuels 2025, 6(2), 46; https://doi.org/10.3390/fuels6020046 - 5 Jun 2025
Cited by 1 | Viewed by 480
Abstract
This study experimentally investigates various flow field designs for a direct ethanol-based proton exchange membrane (PEM) fuel cell operated at a temperature above the vaporization temperature of water. It expands the designs of flow fields investigated for high-temperature (HT) direct ethanol fuel cells [...] Read more.
This study experimentally investigates various flow field designs for a direct ethanol-based proton exchange membrane (PEM) fuel cell operated at a temperature above the vaporization temperature of water. It expands the designs of flow fields investigated for high-temperature (HT) direct ethanol fuel cells by comparing four designs. It investigates the performance of these designs at various ethanol concentrations and flow rates. A series of polarization, constant current, and impedance spectroscopy experiments were carried out at different combinations of operating conditions. The result shows that all flow fields provide poorer performance at a high ethanol concentration (6 M), regardless of ethanol inlet flow rates. At a low concentration (3 M), the 2-channel spiral flow field exhibits higher cell power output (12–18% higher) with less mass transport loss and charge transfer resistance compared to other flow fields, although it has some voltage instability. As such, it is identified as a promising design, particularly for higher-power applications. The 4-channel serpentine, dual-triangle sandwich, and hybrid flow fields offer similar cell power output (max power: ~23 mW/cm2) and cell potentials. However, the cell potential instability and mass transport losses are higher in the hybrid flow field compared to the other two designs. Thus, it is not as promising a design for ethanol-based HT-PEM fuel cells. Since the dual-triangle has similar performance to the 4-channel serpentine, it could be an alternative to the serpentine for ethanol-based HT-PEM fuel cells. Full article
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23 pages, 2792 KiB  
Article
Enhanced Electrocatalytic Performance of Nickel-Cobalt-Titanium Dioxide-Embedded Carbon Nanofibers for Direct Alcohol Fuel Cells
by Wael M. Mohammed, Mahmoud A. Mohamed, Mohamed O. Abdel-Hamed and Esam E. Abdel-Hady
J. Compos. Sci. 2025, 9(3), 125; https://doi.org/10.3390/jcs9030125 - 10 Mar 2025
Cited by 1 | Viewed by 1492
Abstract
This study focuses on making non-precious electrocatalysts for improving the performance of Direct Alcohol Fuel Cells (DAFCs). Specifically, it examines the oxidation of ethanol and methanol. Conventional platinum-based catalysts are expensive and suffer from problems such as degradation and poisoning. To overcome these [...] Read more.
This study focuses on making non-precious electrocatalysts for improving the performance of Direct Alcohol Fuel Cells (DAFCs). Specifically, it examines the oxidation of ethanol and methanol. Conventional platinum-based catalysts are expensive and suffer from problems such as degradation and poisoning. To overcome these challenges, we fabricated tri-metallic catalysts composed of nickel, cobalt, and titanium dioxide (TiO2) embedded in carbon nanofibers (CNFs). The synthesis included electrospinning and subsequent carbonization as well as optimization of parameters to achieve uniform nanofiber morphology and high surface area. Electrochemical characterization revealed that the incorporation of TiO2 significantly improved electrocatalytic activity for ethanol and methanol oxidation, with current densities increasing from 57.8 mA/cm2 to 74.2 mA/cm2 for ethanol and from 38.69 mA/cm2 to 60.39 mA/cm2 for methanol as the TiO2 content increased. The catalysts showed excellent stability, with the TiO2-enriched sample (T2) showing superior performance during longer cycling tests. Chronoamperometry and electrochemical impedance spectroscopy are used to examine the stability of the catalysts and the dynamics of the charge carriers. Impedance spectroscopy indicated reduced charge transfer resistance, confirming enhanced activities. These findings suggest that the synthesized non-precious electrocatalysts can serve as effective alternatives to platinum-based materials, offering a promising pathway for the development of cost-efficient and durable fuel cells. Research highlights non-precious metal catalysts for sustainable fuel cell technologies. Full article
(This article belongs to the Section Nanocomposites)
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11 pages, 4049 KiB  
Article
Yeast-Based Direct Catalytic Ethanol Fuel Cell Biosensors: A Batch Analysis Apparatus Combined with Chemometrics for Qualitative Carbohydrate Detection
by Mauro Tomassetti, Federico Marini, Corrado Di Natale, Mauro Castrucci and Luigi Campanella
Biosensors 2025, 15(2), 96; https://doi.org/10.3390/bios15020096 - 8 Feb 2025
Cited by 1 | Viewed by 822
Abstract
A novel strategy for the qualitative analysis of carbohydrates is developed, utilizing a direct catalytic fuel cell (DCFC) as a sensor, combined with chemometric tools for processing the resulting response curves. Specifically, carbohydrate solutions were incubated with yeast to produce alcohol, and the [...] Read more.
A novel strategy for the qualitative analysis of carbohydrates is developed, utilizing a direct catalytic fuel cell (DCFC) as a sensor, combined with chemometric tools for processing the resulting response curves. Specifically, carbohydrate solutions were incubated with yeast to produce alcohol, and the corresponding current decay trends were measured using a direct catalytic fuel cell designed for ethanol detection. Multiple data processing approaches were then evaluated. Initially, the entire set of data points from the response curves was analyzed using principal component analysis (PCA). To reduce analysis time, chemometric processing was subsequently restricted to the initial portion of the response curves. Finally, to enhance the results, the current decay curves were analyzed in conjunction with the linear fitting parameters derived from the quasi-linear region of the initial response curves, utilizing the common dimension (ComDim) algorithm. Full article
(This article belongs to the Section Biosensor and Bioelectronic Devices)
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16 pages, 4793 KiB  
Article
Simulation of Surface Segregation in Nanoparticles of Pt-Pd Alloys
by Jose Brito Correia and Ana Isabel de Sá
Crystals 2025, 15(1), 53; https://doi.org/10.3390/cryst15010053 - 7 Jan 2025
Cited by 5 | Viewed by 1101
Abstract
Platinum (Pt) and palladium (Pd) are crucial in hydrogen energy technologies, especially in fuel cells, due to their high catalytic activity and chemical stability. Pt-Pd nanoparticles, produced through various methods, enhance catalytic performance based on their size, shape, and composition. These nanocatalysts excel [...] Read more.
Platinum (Pt) and palladium (Pd) are crucial in hydrogen energy technologies, especially in fuel cells, due to their high catalytic activity and chemical stability. Pt-Pd nanoparticles, produced through various methods, enhance catalytic performance based on their size, shape, and composition. These nanocatalysts excel in direct methanol fuel cells (DMFCs) and direct ethanol fuel cells (DEFCs) by promoting alcohol oxidation and reducing CO poisoning. Pt-Pd catalysts are also being explored for their oxygen reduction reaction (ORR) on the cathodic side of fuel cells, showing higher activity and stability than pure platinum. Molecular dynamics (MD) simulations have been conducted to understand the structural and surface energy effects of PdPt nanoparticles, revealing phase separation and chemical ordering, which are critical for optimizing these catalysts. Pd migration to the surface layer in Pt-Pd alloys minimizes the overall potential energy through the formation of Pd surface monolayers and Pt-Pd bonds, leading to a lower surface energy for intermediate compositions compared to that of the pure elements. The potential energy, calculated from MD simulations, increases with a decreasing particle size due to surface creation, indicating higher reactivity for smaller particles. A general contraction of the average distance to the nearest neighbour atoms was determined for the top surface layers within the nanoparticles. This research highlights the significant impact of Pd segregation on the structural and surface energy properties of Pt-Pd nanoparticles. The formation of Pd monolayers and the resulting core–shell structures influence the catalytic activity and stability of these nanoparticles, with smaller particles exhibiting higher surface energy and reactivity. These findings provide insights into the design and optimization of Pt-Pd nanocatalysts for various applications. Full article
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13 pages, 4781 KiB  
Article
Low-Loaded Pt Nanoparticles Supported on Electrochemically Exfoliated Graphene as a Sustainable Catalyst for Electrochemical Ethanol Oxidation
by Irina Srejić, Aleksandar Maksić, Mirjana Novaković, Jelena Potočnik, Lazar Rakočević, Sanja Živković and Milutin Smiljanić
Sustainability 2024, 16(18), 8189; https://doi.org/10.3390/su16188189 - 20 Sep 2024
Cited by 2 | Viewed by 1309
Abstract
Securing ever-increasing energy demands while reducing resilience on fossil fuels is a major task of modern society. Fuel cells are devices in which the chemical energy of various fuels can be converted into clean electricity. Direct ethanol fuel cells (DEFC) are increasingly popular [...] Read more.
Securing ever-increasing energy demands while reducing resilience on fossil fuels is a major task of modern society. Fuel cells are devices in which the chemical energy of various fuels can be converted into clean electricity. Direct ethanol fuel cells (DEFC) are increasingly popular for their eco-friendliness and significantly easier liquid fuel manipulation compared to hydrogen-fed fuel cells. Carbon-supported Pt nanoparticles are considered reference catalysts for fuel oxidation in DEFCs. Several challenges hinder DEFC commercialization: high Pt-loading, Pt poisoning by CO intermediates, and the instability of the Pt and carbon supports. This work demonstrates an efficient electrocatalyst for ethanol oxidation reaction (EOR) composed of Pt nanoparticles supported on electrochemically exfoliated graphene (Pt/el-rGO). Graphene was obtained through anodic electrochemical exfoliation using graphitic tape as the anode, while Pt nanoparticles were synthesized using chemical reduction with formic acid. As-obtained Pt/el-rGO with only 7.5 wt.% Pt was characterized using TEM, SEM, and XPS. Pt/el-rGO exhibited notably higher EOR catalytic activity in an alkaline electrolyte than the Pt/C benchmark. This enhancement can be linked with the functional groups present on the graphene support, which facilitate ethanol dehydrogenation as the first step in the EOR mechanism and thus enhance reaction kinetics on Pt-active sites. Full article
(This article belongs to the Section Energy Sustainability)
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23 pages, 5014 KiB  
Article
Design and Performance of CuNi-rGO and Ag-CuNi-rGO Composite Electrodes for Use in Fuel Cells
by Mohamed Shaban, Aya Mohamed, Mohamed G. M. Kordy, Hamad AlMohamadi, M. F. Eissa and Hany Hamdy
Catalysts 2024, 14(8), 551; https://doi.org/10.3390/catal14080551 - 22 Aug 2024
Cited by 2 | Viewed by 1582
Abstract
This work developed new electrocatalysts for direct alcohol oxidation fuel cells (DAFCs) by using graphene and reduced graphene oxides (GO and rGO) as supporting nanomaterials for copper–nickel (CuNi) nanocomposites. The manufacture of CuNi, CuNi-GO, and CuNi-rGO nanocomposites was realized through the adaptation of [...] Read more.
This work developed new electrocatalysts for direct alcohol oxidation fuel cells (DAFCs) by using graphene and reduced graphene oxides (GO and rGO) as supporting nanomaterials for copper–nickel (CuNi) nanocomposites. The manufacture of CuNi, CuNi-GO, and CuNi-rGO nanocomposites was realized through the adaptation of Hummer’s method and hydrothermal techniques, with subsequent analysis using a range of analytical tools. The electrocatalytic behavior of these materials in DAFCs, with methanol and ethanol as the fuels, was scrutinized through various methods, including cyclic voltammetry, linear sweep, chronoamperometry, and electrochemical impedance spectroscopy. This investigation also assessed the stability and charge transfer dynamics. The rGO-based CuNi nanocomposite demonstrated a remarkable performance boost, showing increases of approximately 319.6% for methanol and 252.6% for ethanol oxidation compared to bare CuNi. The integration of silver nanoparticles into the Ag-CuNi-rGO electrode led to a current density surge to 679.3 mA/g, which signifies enhancements of 254.2% and 812.6% relative to the CuNi-rGO and CuNi electrodes, respectively. These enhancements are ascribed to the augmented densities of hot sites and the synergistic interactions within the nanocatalysts. The findings underscore the potential of Ag and rGO as effective supports for CuNi nanocomposites, amplifying their catalytic efficiency in DAFC applications. Full article
(This article belongs to the Section Nanostructured Catalysts)
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16 pages, 3101 KiB  
Article
Candle Soot as a Novel Support for Nickel Nanoparticles in the Electrocatalytic Ethanol Oxidation
by Muliani Mansor, Siti Noorleila Budiman, Azran Mohd Zainoodin, Mohd Paad Khairunnisa, Shinya Yamanaka, Nurfatehah Wahyuny Che Jusoh and Shahira Liza
Nanomaterials 2024, 14(12), 1042; https://doi.org/10.3390/nano14121042 - 18 Jun 2024
Cited by 2 | Viewed by 2082
Abstract
The enhancement of carbon-supported components is a crucial factor in augmenting the interplay between carbon-supported and metal-active components in the utilization of catalysts for direct ethanol fuel cells (DEFCs). Here, we propose a strategy for designing a catalyst by modifying candle soot (CS) [...] Read more.
The enhancement of carbon-supported components is a crucial factor in augmenting the interplay between carbon-supported and metal-active components in the utilization of catalysts for direct ethanol fuel cells (DEFCs). Here, we propose a strategy for designing a catalyst by modifying candle soot (CS) and loading nickel onto ordered carbon soot. The present study aimed to investigate the effect of the Ni nanoparticles content on the electrocatalytic performance of Ni–CS, ultimately leading to the identification of a maximum composition. The presence of an excessive quantity of nickel particles leads to a decrease in the number of active sites within the material, resulting in sluggishness of the electron transfer pathway. The electrocatalyst composed of nickel and carbon support, with a nickel content of 20 wt%, has demonstrated a noteworthy current activity of 18.43 mA/cm2, which is three times that of the electrocatalyst with a higher nickel content of 25 wt%. For example, the 20 wt% Ni–CS electrocatalytic activity was found to be good, and it was approximately four times higher than that of 20 wt% Ni–CB (nickel–carbon black). Moreover, the chronoamperometry (CA) test demonstrated a reduction in current activity of merely 65.80% for a 20 wt% Ni–CS electrocatalyst, indicating electrochemical stability. In addition, this demonstrates the great potential of candle soot with Ni nanoparticles to be used as a catalyst in practical applications. Full article
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13 pages, 4598 KiB  
Article
Laser Irradiation Synthesis of AuPd Alloy with Decreased Alloying Degree for Efficient Ethanol Oxidation Reaction
by Nan Jiang, Liye Zhu, Peng Liu, Pengju Zhang, Yuqi Gan, Yan Zhao and Yijian Jiang
Materials 2024, 17(8), 1876; https://doi.org/10.3390/ma17081876 - 18 Apr 2024
Cited by 3 | Viewed by 1491
Abstract
The preparation of electrocatalysts with high performance for the ethanol oxidation reaction is vital for the large-scale commercialization of direct ethanol fuel cells. Here, we successfully synthesized a high-performance electrocatalyst of a AuPd alloy with a decreased alloying degree via pulsed laser irradiation [...] Read more.
The preparation of electrocatalysts with high performance for the ethanol oxidation reaction is vital for the large-scale commercialization of direct ethanol fuel cells. Here, we successfully synthesized a high-performance electrocatalyst of a AuPd alloy with a decreased alloying degree via pulsed laser irradiation in liquids. As indicated by the experimental results, the photochemical effect-induced surficial deposition of Pd atoms, combined with the photothermal effect-induced interdiffusion of Au and Pd atoms, resulted in the formation of AuPd alloys with a decreased alloying degree. Structural characterization reveals that L-AuPd exhibits a lower degree of alloying compared to C-AuPd prepared via the conventional co-reduction method. This distinct structure endows L-AuPd with outstanding catalytic activity and stability in EOR, achieving mass and specific activities as high as 16.01 A mgPd−1 and 20.69 mA cm−2, 9.1 and 5.2 times than that of the commercial Pd/C respectively. Furthermore, L-AuPd retains 90.1% of its initial mass activity after 300 cycles. This work offers guidance for laser-assisted fabrication of efficient Pd-based catalysts in EOR. Full article
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17 pages, 2842 KiB  
Article
Improved Sugarcane-Based Fermentation Processes by an Industrial Fuel-Ethanol Yeast Strain
by Gabriela Muller, Victor R. de Godoy, Marcelo G. Dário, Eduarda H. Duval, Sergio L. Alves-Jr, Augusto Bücker, Carlos A. Rosa, Barbara Dunn, Gavin Sherlock and Boris U. Stambuk
J. Fungi 2023, 9(8), 803; https://doi.org/10.3390/jof9080803 - 29 Jul 2023
Cited by 8 | Viewed by 3142
Abstract
In Brazil, sucrose-rich broths (cane juice and/or molasses) are used to produce billions of liters of both fuel ethanol and cachaça per year using selected Saccharomyces cerevisiae industrial strains. Considering the important role of feedstock (sugar) prices in the overall process economics, to [...] Read more.
In Brazil, sucrose-rich broths (cane juice and/or molasses) are used to produce billions of liters of both fuel ethanol and cachaça per year using selected Saccharomyces cerevisiae industrial strains. Considering the important role of feedstock (sugar) prices in the overall process economics, to improve sucrose fermentation the genetic characteristics of a group of eight fuel-ethanol and five cachaça industrial yeasts that tend to dominate the fermentors during the production season were determined by array comparative genomic hybridization. The widespread presence of genes encoding invertase at multiple telomeres has been shown to be a common feature of both baker’s and distillers’ yeast strains, and is postulated to be an adaptation to sucrose-rich broths. Our results show that only two strains (one fuel-ethanol and one cachaça yeast) have amplification of genes encoding invertase, with high specific activity. The other industrial yeast strains had a single locus (SUC2) in their genome, with different patterns of invertase activity. These results indicate that invertase activity probably does not limit sucrose fermentation during fuel-ethanol and cachaça production by these industrial strains. Using this knowledge, we changed the mode of sucrose metabolism of an industrial strain by avoiding extracellular invertase activity, overexpressing the intracellular invertase, and increasing its transport through the AGT1 permease. This approach allowed the direct consumption of the disaccharide by the cells, without releasing glucose or fructose into the medium, and a 11% higher ethanol production from sucrose by the modified industrial yeast, when compared to its parental strain. Full article
(This article belongs to the Special Issue New Perspectives on Industrial Yeasts)
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14 pages, 1939 KiB  
Article
Cryogels from Pt/γ-Fe2O3 and Pd/γ-Fe2O3 NPs as Promising Electrocatalysts for Ethanol Oxidation Reaction
by Hadir Borg, Irene Morales, Daniel Kranz, Nadja C. Bigall and Dirk Dorfs
Catalysts 2023, 13(7), 1074; https://doi.org/10.3390/catal13071074 - 6 Jul 2023
Cited by 4 | Viewed by 2033
Abstract
Cryogels from noble metal NPs have proven to be highly efficient catalysts due to their high specific surface area which increases the mass transfer channels and catalytic active sites. By using metal oxides as co-catalysts, the costs of the material can be significantly [...] Read more.
Cryogels from noble metal NPs have proven to be highly efficient catalysts due to their high specific surface area which increases the mass transfer channels and catalytic active sites. By using metal oxides as co-catalysts, the costs of the material can be significantly reduced, while the catalytic activity can remain the same or even improve due to synergetic effects. In this work, we synthesize different cryogel thin films supported on modified ITO substrates from Pt, Pd nanoparticles (NPs), and mixtures of these noble metals with γ-Fe2O3 NPs in a very low concentration (1 wt% of the noble metal). Structural and elemental analysis of the samples are performed, along with the measurement and analysis of their catalytic activity. The electrocatalytic activity of the cryogels towards ethanol oxidation reaction (EOR) in alkaline media was evaluated by means of cyclic voltammetry. By mixing γ-Fe2O3 NPs with Pt or Pd NPs in the cryogel structure, we observe increased tolerance against poisonous surface intermediates produced during the EOR. Moreover, we observe an increase in the catalytic activity towards EOR in the case of the 1 wt% Pd/γ-Fe2O3 cryogel, making them promising materials for the development of direct ethanol fuel cells. Full article
(This article belongs to the Special Issue Catalysts and Photocatalysts Based on Mixed Metal Oxides)
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11 pages, 2522 KiB  
Article
Unexpected Negative Performance of PdRhNi Electrocatalysts toward Ethanol Oxidation Reaction
by Ahmed ElSheikh and James McGregor
Micromachines 2023, 14(5), 957; https://doi.org/10.3390/mi14050957 - 27 Apr 2023
Cited by 2 | Viewed by 1895
Abstract
Direct ethanol fuel cells (DEFCs) need newly designed novel affordable catalysts for commercialization. Additionally, unlike bimetallic systems, trimetallic catalytic systems are not extensively investigated in terms of their catalytic potential toward redox reactions in fuel cells. Furthermore, the Rh potential to break the [...] Read more.
Direct ethanol fuel cells (DEFCs) need newly designed novel affordable catalysts for commercialization. Additionally, unlike bimetallic systems, trimetallic catalytic systems are not extensively investigated in terms of their catalytic potential toward redox reactions in fuel cells. Furthermore, the Rh potential to break the ethanol rigid C-C bond at low applied potentials, and therefore enhance the DEFC efficiency and CO2 yield, is controversial amongst researchers. In this work, two PdRhNi/C, Pd/C, Rh/C and Ni/C electrocatalysts are synthesized via a one-step impregnation process at ambient pressure and temperature. The catalysts are then applied for ethanol electrooxidation reaction (EOR). Electrochemical evaluation is performed using cyclic voltammetry (CV) and chronoamperometry (CA). Physiochemical characterization is pursued using X-ray diffraction (XRD), transmission electron microscope (TEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS). Unlike Pd/C, the prepared Rh/C and Ni/C do not show any activity for (EOR). The followed protocol produces alloyed dispersed PdRhNi nanoparticles of 3 nm in size. However, the PdRhNi/C samples underperform the monometallic Pd/C, even though the Ni or Rh individual addition to it enhances its activity, as reported in the literature herein. The exact reasons for the low PdRhNi performance are not fully understood. However, a reasonable reference can be given about the lower Pd surface coverage on both PdRhNi samples according to the XPS and EDX results. Furthermore, adding both Rh and Ni to Pd exercises compressive strain on the Pd lattice, noted by the PdRhNi XRD peak shift to higher angles. Full article
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16 pages, 3885 KiB  
Article
A Direct Catalytic Ethanol Fuel Cell (DCEFC) Modified by LDHs, or by Catalase-LDHs, and Improvement in Its Kinetic Performance: Applications for Human Saliva and Disinfectant Products for COVID-19
by Mauro Tomassetti, Riccardo Pezzilli, Claudio Leonardi, Giuseppe Prestopino, Corrado Di Natale, Luigi Campanella and Pier Gianni Medaglia
Biosensors 2023, 13(4), 441; https://doi.org/10.3390/bios13040441 - 30 Mar 2023
Cited by 2 | Viewed by 2143
Abstract
In this work, it has been experimentally proven that the kinetic performance of a common Direct Catalytic Ethanol Fuel Cell (DCEFC) can be increased by introducing nanostructured (ZnII,AlIII(OH)2)+NO3·H2O Layered Double [...] Read more.
In this work, it has been experimentally proven that the kinetic performance of a common Direct Catalytic Ethanol Fuel Cell (DCEFC) can be increased by introducing nanostructured (ZnII,AlIII(OH)2)+NO3·H2O Layered Double Hydroxides (LDHs) into the anode compartment. Carrying out the measurements with the open-circuit voltage method and using a kinetic format, it has been shown that the introduction of LDHs in the anodic compartment implies a 1.3-fold increase in the calibration sensitivity of the method. This improvement becomes even greater in the presence of hydrogen peroxide in a solution. Furthermore, we show that the calibration sensitivity increased by 8-times, when the fuel cell is modified by the enzyme catalase, crosslinked on LDHs and in the presence of hydrogen peroxide. The fuel cell, thus modified (with or without enzyme), has been used for analytical applications on real samples, such as biological (human saliva) and hand disinfectant samples, commonly used for the prevention of COVID-19, obtaining very positive results from both analytical and kinetic points of view on ethanol detection. Moreover, if the increase in the calibration sensitivity is of great importance from the point of view of analytical applications, it must be remarked that the increase in the speed of the ethanol oxidation process in the fuel cell can also be extremely useful for the purposes of improving the energy performance of a DCEFC. Full article
(This article belongs to the Special Issue New Biosensors and Nanosensors)
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15 pages, 1837 KiB  
Article
Glucose Conversion for Biobutanol Production from Fresh Chlorella sorokiniana via Direct Enzymatic Hydrolysis
by Jinzhi Yang, Di Cai, Xudong Liu, Liqi Zhu, Changwei Zhang, Qing Peng, Yanxia Han, Guozhen Liu and Ming Yang
Fermentation 2023, 9(3), 284; https://doi.org/10.3390/fermentation9030284 - 14 Mar 2023
Cited by 7 | Viewed by 3452
Abstract
Microalgae, which accumulate considerable carbohydrates, are a potential source of glucose for biofuel fermentation. In this study, we investigated the enzymatic hydrolysis efficiency of wet microalgal biomass compared with freeze-dried and oven-dried biomasses, both with and without an acidic pretreatment. With the dilute [...] Read more.
Microalgae, which accumulate considerable carbohydrates, are a potential source of glucose for biofuel fermentation. In this study, we investigated the enzymatic hydrolysis efficiency of wet microalgal biomass compared with freeze-dried and oven-dried biomasses, both with and without an acidic pretreatment. With the dilute sulfuric acid pretreatment followed by amy (α-amylase and amyloglucosidase) and cellulase hydrolysis, approximately 95.4% of the glucose was recovered; however, 88.5% was released by the pretreatment with 2% (w/v) sulfuric acid, which indicates the potential of the acids for direct saccharification process. There were no considerable differences in the glucose yields among the three kinds of materials. In the direct amy hydrolysis without any pretreatment, a 78.7% glucose yield was obtained, and the addition of cellulase had no significant effect on the hydrolysis to glucose. Compared with the oven-dried biomass, the wet biomass produced a substantially higher glucose yield, which is possibly because the cross-linked cells of the oven-dried biomass prevented the accessibility of the enzymes. According to the results, the fresh microalgal biomass without cell disruption can be directly used for enzymatic hydrolysis to produce glucose. The enzymatic hydrolysate of the wet microalgal biomass was successfully used for acetone–butanol–ethanol (ABE) fermentation, which produced 7.2 g/L of ABE, indicating the application potential of wet microalgae in the bioalcohol fuel fermentation process. Full article
(This article belongs to the Special Issue Algae—the Medium of Bioenergy Conversion)
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20 pages, 5592 KiB  
Article
Efficiency of Neat and Quaternized-Cellulose Nanofibril Fillers in Chitosan Membranes for Direct Ethanol Fuel Cells
by Maša Hren, Damjan Makuc, Janez Plavec, Michaela Roschger, Viktor Hacker, Boštjan Genorio, Mojca Božič and Selestina Gorgieva
Polymers 2023, 15(5), 1146; https://doi.org/10.3390/polym15051146 - 24 Feb 2023
Cited by 7 | Viewed by 2392
Abstract
In this work, fully polysaccharide based membranes were presented as self-standing, solid polyelectrolytes for application in anion exchange membrane fuel cells (AEMFCs). For this purpose, cellulose nanofibrils (CNFs) were modified successfully with an organosilane reagent, resulting in quaternized CNFs (CNF (D)), as shown [...] Read more.
In this work, fully polysaccharide based membranes were presented as self-standing, solid polyelectrolytes for application in anion exchange membrane fuel cells (AEMFCs). For this purpose, cellulose nanofibrils (CNFs) were modified successfully with an organosilane reagent, resulting in quaternized CNFs (CNF (D)), as shown by Fourier Transform Infrared Spectroscopy (FTIR), Carbon-13 (C13) nuclear magnetic resonance (13C NMR), Thermogravimetric Analysis (TGA)/Differential Scanning Calorimetry (DSC), and ζ-potential measurements. Both the neat (CNF) and CNF(D) particles were incorporated in situ into the chitosan (CS) membrane during the solvent casting process, resulting in composite membranes that were studied extensively for morphology, potassium hydroxide (KOH) uptake and swelling ratio, ethanol (EtOH) permeability, mechanical properties, ionic conductivity, and cell performance. The results showed higher Young’s modulus (119%), tensile strength (91%), ion exchange capacity (177%), and ionic conductivity (33%) of the CS-based membranes compared to the commercial Fumatech membrane. The addition of CNF filler improved the thermal stability of the CS membranes and reduced the overall mass loss. The CNF (D) filler provided the lowest (4.23 × 10−5 cm2 s−1) EtOH permeability of the respective membrane, which is in the same range as that of the commercial membrane (3.47 × 10−5 cm2s−1). The most significant improvement (~78%) in power density at 80 °C was observed for the CS membrane with neat CNF compared to the commercial Fumatech membrane (62.4 mW cm−2 vs. 35.1 mW cm−2). Fuel cell tests showed that all CS-based anion exchange membranes (AEMs) exhibited higher maximum power densities than the commercial AEMs at 25 °C and 60 °C with humidified or non-humidified oxygen, demonstrating their potential for low-temperature direct ethanol fuel cell (DEFC) applications. Full article
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14 pages, 7808 KiB  
Article
ZIF-67-Derived NiCo-Layered Double Hydroxide@Carbon Nanotube Architectures with Hollow Nanocage Structures as Enhanced Electrocatalysts for Ethanol Oxidation Reaction
by Yixuan Li, Yanqi Xu, Cunjun Li, Wenfeng Zhu, Wei Chen, Yufei Zhao, Ruping Liu and Linjiang Wang
Molecules 2023, 28(3), 1173; https://doi.org/10.3390/molecules28031173 - 25 Jan 2023
Cited by 15 | Viewed by 3116
Abstract
The rational design of efficient Earth-abundant electrocatalysts for the ethanol oxidation reaction (EOR) is the key to developing direct ethanol fuel cells (DEFCs). Among these, the smart structure is highly demanded for highly efficient and stable non-precious electrocatalysts based on transition metals (such [...] Read more.
The rational design of efficient Earth-abundant electrocatalysts for the ethanol oxidation reaction (EOR) is the key to developing direct ethanol fuel cells (DEFCs). Among these, the smart structure is highly demanded for highly efficient and stable non-precious electrocatalysts based on transition metals (such as Ni, Co, and Fe). In this work, high-performance NiCo-layered double hydroxide@carbon nanotube (NiCo-LDH@CNT) architectures with hollow nanocage structures as electrocatalysts for EOR were prepared via sacrificial ZIF-67 templates on CNTs. Comprehensive structural characterizations revealed that the as-synthesized NiCo-LDH@CNTs architecture displayed 3D hollow nanocages of NiCo-LDH and abundant interfacial structure between NiCo-LDH and CNTs, which could not only completely expose active sites by increasing the surface area but also facilitate the electron transfer during the electrocatalytic process, thus, improving EOR activity. Benefiting from the 3D hollow nanocages and interfacial structure fabricated by the sacrificial ZIF-67-templated method, the NiCo-LDH@CNTs-2.5% architecture exhibited enhanced electrocatalytic activity for ethanol oxidation compared to single-component NiCo-LDH, where the peak current density was 11.5 mA·cm−2, and the jf/jb value representing the resistance to catalyst poisoning was 1.72 in an alkaline environment. These results provide a new perspective on the fabrication of non-precious metal electrocatalysts for EOR in DEFCs. Full article
(This article belongs to the Special Issue Catalysis, Electronics, Energy and Health at Nanoscale Domain)
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