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    Electrochemical characterization of electrolyte supported solid oxide electrolysis cell during CO2/H2O co-electrolysis
    (Springer Science and Business Media Deutschland GmbH, 2024) Shirasangi, R.; Prasad Dasari, H.P.; Saidutta, M.B.
    High-temperature co-electrolysis is studied on electrolyte-supported NiO-YSZ/NiO-SDC/ScSZ/LSCF-GDC/LSCF (NiO: Nickel Oxide, YSZ: Yttria-stabilized zirconia, SDC: Samarium-doped ceria, ScSZ: Scandia-stabilized zirconia, LSCF: Lanthanum Strontium Cobalt Ferrite, GDC: Gadolinium-doped ceria) button cell. Electrochemical impedance spectroscopy (EIS) was recorded under open-circuit voltage (OCV) and co-electrolysis mode over various operating conditions, including temperature, water vapor content, and applied voltage. Interfacial polarization resistance (Rp) is obtained from peak arcs located in the three regions: gas conversion resistance (Region I (0.01 to 0.1 Hz)), gas diffusion resistance (Region II (0.1 to 100 Hz)) and air electrode charge transfer resistance (Region III (100 to 10,000 Hz)). As the temperature increased from 700 to 850 oC, Rp decreased from 18.15 to 3.32 Ω.cm2 at 1.3 V for 10%CO2/3%H2O. From the Distribution of relaxation times (DRT) studies, one additional peak, P5 (fuel gas conversion or gas-phase diffusion in the pores of the air electrode), is observed, and Region III (100 to 10,000 Hz) consists of two additional peaks: P1 (ionic transport coupled with gas diffusion close to triple phase boundaries (TPBs)) and P2 (fuel electrode charge transfer reaction), which were not clearly distinguished from EIS. Region II dominates in the overall polarization resistance. At 800 oC, for 10%CO2/3%H2O, the Rp decreased from 6.78 to 4.82 Ω.cm2, with an increase in the applied voltage from 1.3 to 1.5 V. At 800oC/1.5 V, the Rp values are 4.41, 8.09, and 6.77 Ω.cm2 for H2O, CO2, and co-electrolysis. At 800 ºC/1.5 V, with an increase in the water vapor content from 3%H2O to 15%H2O, there is not much change in the Rp value; therefore, 10%H2O is sufficient. H2 consumption is between 23 and 36%, depending on the temperature at OCV. At 800 °C for (10%H2/10%CO2/10%H2O), co-electrolysis occurs at applied voltage, along with Reverse water gas shift (RWGS) reaction. Graphical Abstract: (Figure presented.) © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
  • Item
    CO2 concentration effects on CO2/H2O co-electrolysis in a solid oxide electrolysis button cell
    (Springer Science and Business Media Deutschland GmbH, 2025) Shirasangi, R.; Prasad Dasari, H.P.; Saidutta, M.B.
    Abstract: The influence of CO2 gas concentration on the co-electrolysis performance of an electrolyte-supported button cell (NiO-YSZ/NiO-SDC/ScSZ/LSCF-GDC/LSCF) was investigated. At 800 oC/1.5V, the interfacial polarization resistance (Rp) values for 10%CO2/15%H2O and 30%CO2/15%H2O are 7.19 and 26.91 ?.cm2, respectively. CO2 gas concentration significantly affects the Rp value. Gas diffusion resistance is dominant in the overall polarization resistance. As the CO2 concentration increases (10%?30%), H2 consumption increases, indicating RWGS dominance. For 30% CO2/15% H2O, CO2 out is slightly more than the input value due to the WGS and Boudouard reactions. As the applied voltage value increases from OCV, the H2 residue increases. H2O and CO2 co-electrolysis occurs at 1.5 V. The post-test XRD and Raman spectra results show NiO reduction and metallic Ni appearance. The post-test FE-SEM micrographs show no delamination at the air electrode/electrolyte interface, and carbon deposition is observed in the composite fuel electrode layer. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.