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- Ajmal Khan, Muhammad, et al.
(author)
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Comparative study of the nano-composite electrolytes based on samaria-doped ceria for low temperature solid oxide fuel cells (LT-SOFCs)
- 2013
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In: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 38:36, s. 16524-16531
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Journal article (peer-reviewed)abstract
- Ceria-based electrolyte materials have great potential in low and intermediate temperature solid oxide fuel cell applications. In the present study, three types of ceria-based nanocomposite electrolytes (LNK-SDC, LN-SDC and NK-SDC) were synthesized. One-step co-precipitation method was adopted and different techniques were applied to characterize the obtained ceria-based nano-composite electrolyte materials. TGA, XRD and SEM were used to analyze the thermal effect, crystal structure and morphology of the materials. Cubic fluorite structures have been observed in all composite electrolytes. Furthermore, the crystallite sizes of the LN-SDC, NK-SDC, LNK-SDC were calculated by Scherrer formula and found to be in the range 20 nm, 21 nm and 19 nm, respectively. These values emphasize a good agreement with the SEM results. The ionic conductivities were measured using EIS (Electrochemical Impedance Spectroscopy) with two-probe method and the activation energies were also calculated using Arrhenius plot. The maximum power density was achieved 484 mW/cm(2) of LNK-SDC electrolyte at 570 degrees C using the LiCuZnNi oxide electrodes.
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- Bohn Lima, Raquel, et al.
(author)
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Modeling and studies in direct carbon-biomass fuel cell for power generation
- 2013
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In: Abstracts of Papers, 245th ACS National Meeting & Exposition, New Orleans, LA, United States, April 7-11, 2013. ; , s. ENFL-526-
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Conference paper (other academic/artistic)abstract
- Several factors such as the global energy supply security and the need for generating efficient and clean energy have increased the interest in the research related to alternative fuel and energy systems. Among these alternative systems, the biomass-fuelled integrated Direct Carbon Fuel Cell (DCFC) with solid oxide fuel cell (SOFC)/molten carbonate fuel cell (MCFC) systems have been identified as one of key energy technologies for the future since it combines the merits of renewable energy sources and carbon/hydrogen energy systems.The modeling of energy systems plays a crucial role in the estn. of the performance and selection of the configuration and the operation parameters of these systems. In the case of integrated DCFC - SOFC/MCFC systems, there are many aspects that should be considered for a complete and robust model. The lack of such a model for integrated DCFC - SOFC/MCFC and biomass systems in the literature have been the main motivation for this study.
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- Khan, M. Ajmal, et al.
(author)
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Effect of titania concentration on the grain boundary conductivity of calcium-doped ceria electrolyte
- 2014
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In: Ceramics International. - : Elsevier BV. - 0272-8842 .- 1873-3956. ; 40:7, s. 9775-9781
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Journal article (peer-reviewed)abstract
- A solid-state technique was used to synthesize ceria-based (CDC-xT, in which x=0-1 mol%) solid electrolyte ceramics. The effects of doping the ceramic solid electrolyte (CDC) with titanium oxide were studied with regard to densification, crystal structure, morphology, electro-impedance spectroscopy and fuel cell performance. TiO2 doping afforded materials a 95% relative density at 940 degrees C, approximately 200 degrees C lower than the temperature required without titanium oxide. The addition of titanium oxide (TiO2) reduced the CDC sintering temperature and significantly improved the grain boundary conduction. The minimum grain boundary resistivity was obtained at 0.8 mol% TiO2. X-ray diffraction (XRD) results showed that the lattice parameters enhanced with increased titanium oxide concentrations up to 0.8 mol%, revealing the solubility limit for Caria's fluorite structure. The optimum doping level (0.8 mol%) is provided maximum conductivity. Conductivities were measured using EIS (Electrochemical Impedance Spectroscopy) with a two-probe method, and the activation energies were calculated using the Arrhenius plots. The maximum power density (660 mW/cm(2)) was achieved with CDC 0.8T electrolyte at 650 degrees C using LiCuZnNi oxide electrodes.
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- Lima, Raquel Bohn, et al.
(author)
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Direct lignin fuel cell for power generation
- 2013
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In: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 3:15, s. 5083-5089
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Journal article (peer-reviewed)abstract
- Lignin, the second most abundant component after cellulose in biomass, has been examined in this study as a fuel for direct conversion into electricity using direct carbon fuel cells (DCFC). Two different types of industrial lignins were investigated: Lignosulfonate (LS) and Kraft lignin (KL), in their commercial forms, after their blending with commercial active carbon (AC) or after alteration of their structures by a pH adjustment to pH 10. It was found that the open circuit voltage (OCV) of the DCFC could reach around 0.7 V in most of the trials. Addition of active carbon increased the maximum current density from 43-57 to 83-101 mA cm(-2). The pH adjustment not only increased the maximum current density but also reduced the differences between the two types of lignins, resulting in an OCV of 0.68-0.69 V and a maximum current density of 74-79 mA cm(-2) from both lignins. Typical power density was 12 (for KL + AC) and 24 mW cm(-2) (for LS + AC). It is concluded that a direct lignin fuel cell is feasible and the lignin hydrophilicity is critical for the cell performance.
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- Oyarce, Alejandro, et al.
(author)
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Direct sorbitol proton exchange membrane fuel cell using moderate catalyst loadings
- 2014
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In: Electrochimica Acta. - : Elsevier BV. - 0013-4686 .- 1873-3859. ; 116, s. 379-387
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Journal article (peer-reviewed)abstract
- Recent progress in biomass hydrolysis has made it interesting to study the use of sorbitol for electricity generation. In this study, sorbitol and glucose are used as fuels in proton exchange membrane fuel cells having 0.9 mg cm(-2) PtRu/C at the anode and 0.3 mg cm(-2) Pt/C at the cathode. The sorbitol oxidation was found to have slower kinetics than glucose oxidation. However, at low temperatures the direct sorbitol fuel cell shows higher performance than the direct glucose fuel cell, attributed to a lower degree of catalyst poisoning. The performance of both fuel cells is considerably improved at higher temperatures. High temperatures lower the poisoning, allowing the direct glucose fuel cell to reach a higher performance than the direct sorbitol fuel cell. The mass specific peak power densities of the direct sorbitol and direct glucose fuel cells at 65 degrees C was 3.2 mW Mg-catalyst(-1) and 3.5 mW Mg-catalyst(-1), respectively. Both of these values are one order of magnitude larger than mass specific peak power densities of earlier reported direct glucose fuel cells using proton exchange membranes. Furthermore, both the fuel cells showed a considerably decrease in performance with time, which is partially attributed to sorbitol and glucose crossover poisoning the Pt/C cathode.
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