Faculty Publications
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Item Record-low sintering-temperature (600 °c) of solid-oxide fuel cell electrolyte(Elsevier Ltd, 2016) Prasad Dasari, H.P.; Ahn, K.; Park, S.-Y.; Hong, J.; Kim, H.; Yoon, K.J.; Son, J.-W.; Kim, B.-K.; Lee, H.-W.; Lee, J.-H.One of the major problems arising with Solid-Oxide Fuel Cell (SOFC) electrolyte is conventional sintering which requires a very high temperature (>1300 °C) to fully densify the electrolyte material. In the present study, the sintering temperature of SOFC electrolyte is drastically decreased down to 600 °C. Combinational effects of particle size reduction, liquid-phase sintering mechanism and microwave sintering resulted in achieving full density in such a record-low sintering temperature. Gadolinium doped Ceria (GDC) nano-particles are synthesized by co-precipitation method, Lithium (Li), as an additional dopant, is used as liquid-phase sintering aid. Microwave sintering of this electrolyte material resulted in decreasing the sintering temperature to 600 °C. Micrographs obtained from Scanning/Transmission Electron Microscopy (SEM/TEM) clearly pointed a drastic growth in grain-size of Li-GDC sample (?150 nm) than compared to GDC sample (<30 nm) showing the significance of Li addition. The sintered Li-GDC samples displayed an ionic conductivity of ?1.00 × 10-2 S cm-1 at 600 °C in air and from the conductivity plots the activation energy is found to be 0.53 eV. © 2016 Elsevier B.V. All rights reserved.Item Praseodymium doped ceria as electrolyte material for IT-SOFC applications(Elsevier Ltd, 2018) Shajahan, I.; Ahn, J.; Nair, P.; Medisetti, S.; Patil, S.; Niveditha, V.; Uday Bhaskar Babu, G.; Prasad Dasari, H.P.; Lee, J.-H.Praseodymium-doped ceria (PDC, Ce0.9Pr0.1O2) electrolyte material for intermediate temperature solid oxide fuel cells (IT-SOFCs) has been successfully synthesised by EDTA-citrate method. From X-Ray diffraction (XRD), fluorite structure along with a crystallite size of 5.4 nm is obtained for PDC nanopowder calcined at 350 °C/24 h. Raman spectroscopy confirmed the structure, presence of oxygen vacancies with the manifestation of the main peak at 457 cm?1 and with a secondary peak at 550 cm?1. From Transmission Electron Microscopy (TEM) analysis, the average particle size is around 7–10 nm and selected area electron diffraction (SAED) patterns further confirmed the fluorite structure of PDC nanopowder. The PDC nanopowder displayed a BET surface area of 65 m2/g with a primary particle size of ?13 nm (calculated from BET surface area). Dilatometer studies revealed a multi-step shrinkage behaviour with the multiple peaks at 522, 1171 and 1461 °C which may be originated due to the presence of multiple size hard agglomerates. The PDC electrolyte pellet sintered at 1500 °C displayed an ionic conductivity of 1.213E-03 S cm?1 along with an activation energy of 1.28eV. Instead of a single fluorite structure, XRD of sintered PDC pellet showed multiple structures (Fluorite structure (CeO2) and cubic structure (PrO2). © 2018 Elsevier B.V.Item Surface morphology and phase stability effect of Ceria-Hafnia (CHx) binary metal oxides on soot oxidation activity(Elsevier B.V., 2018) Anjana, A.P.; Prasad Dasari, H.P.; Harshini, H.; Babu, G.U.B.CeO2-HfO2 (CHx) binary metal oxides over whole composition range (0–100%) are synthesised using the EDTA-Citrate method and calcined at 600 °C/5 h. From XRD analysis, the sample series are classified as fluorite (F) phase for CH10-CH30, hybrid (F + M) phase for CH40-CH90 and monoclinic (M) phase for CH100 sample, respectively and the results were further confirmed using Raman spectroscopy. From SEM analysis, a clear surface morphology change is noticed for fluorite, hybrid and monoclinic phases of the CHx binary metal oxides. Further, Selected Area Electron Diffraction (SAED) analysis also confirmed the single and hybrid phases of CHx binary metal oxides. The soot oxidation for the CHx binary metal oxides displayed high catalytic activity for Fluorite phase (CH10 ? CH30) samples and a decrease in catalytic activity is noticed for the Hybrid phase (CH40 ? CH90) samples. The change in catalytic activity coincides with the change in the surface morphology and phase change for the CHx binary metal oxides. Among the Fluorite phase samples, CH10 sample displayed the highest catalytic activity (T50 = 430 °C) with higher surface area (29 m2/g), lower particle size (26 nm), lower degree of agglomeration (? = 2.8) higher surface oxygen concentration (44%). Isothermal-Time-on-stream (ITOS) analysis also showed that the CH10 sample can achieve T50 in a shorter time than compared to other CHx binary metal oxides. Surface morphology and phase stability can also play as key descriptors in screening CHx binary metal oxides for soot oxidation activity. © 2018 Elsevier B.V.Item Ceria-Terbium-based electrospun nanofiber catalysts for soot oxidation activity and its kinetics(Taiwan Institute of Chemical Engineers, 2024) Patil, S.S.; Kumar, R.; Prasad Dasari, H.P.Background: Ceria-based materials have an excellent potential to be catalysts for catalytic three-way converters in the automobile industry. Developing Ceria-based nanofiber catalysts can be a significant approach for further exploring the application of these materials in automobile industries. Methods: In this study, Ag, Cu, or Co doped Ceria–Terbium nanofibers were synthesized using the electrospinning technique. The obtained nanofiber catalysts were characterized using FE-SEM, XRD, FT-Raman Spectroscopy, and BET-BJH analysis and tested for soot oxidation activity and its kinetics. Significant findings: FE-SEM examination reveals that the obtained nanofibers have a diameter ranging from around 100 to 600 nm. CeTbCo nanofibers exhibited a reduced particle size and enhanced pore formation. The XRD investigation revealed that all the nanofibers displayed a face-centered fluorite structure of CeO2. In Raman spectroscopy analysis, CeTbCo nanofibes showed the emergence of a secondary Co3O4 phase. The CeTbCo nanofiber catalyst showed better SBET (specific surface area) (66 m2/g) and average pore size (12.08 nm) and total pore volume (0.223 cc/g)), better soot oxidation activity (T50 = 347 ℃) than other nanofiber catalysts. The CeTbCo nanofiber catalyst exhibited an activation energy of 132 kJ mol−1 and a pre-exponential factor (ln (A)) of 25.63 min−1. © 2024 Taiwan Institute of Chemical Engineers