Intermediate Temperature Solid Oxide Fuel Cells Research Articles

A high-performance composite cathode based on thermal expansion complementation for SOFC

The discrepancy in thermal expansion coefficients (TECs) between the cobalt-based cathode and the electrolyte presents a notable obstacle in attaining optimal performance levels for solid oxide fuel cells (SOFCs). Here we propose to introduce negative thermal expansion (NTE) component Sm0.85Zn0.15MnO3 (SZM) to SrNb0.1Co0.9O3−δ (SNC) cathode to prepare SNC-xSZM (x = 0, 10, 20 and 30 %) composite cathode materials. The impact of incorporating negative thermal expansion material on the composition and properties of the matrix materials were examined by X-ray diffraction, thermal dilatometer, high-resolution transmission electron microscopy, and electrochemical workstation. The results show that SNC-xSZM can achieve more ideal thermal matching with Ce0.8Gd0.2O1.9 (GDC), and the thermal expansion coefficient decreases observably from 25.47 × 10−6 K−1 for x = 0 to 13.74 × 10−6 K−1 for x = 30 %. The optimal comprehensive electrochemical performance is obtained for SNC-20SZM, which possesses the minimum polarization resistance (Rp) of 0.012 Ω cm2 at 700 °C. The SNC-20SZM-based cell shows a maximum peak power density (PPD) of 1.22 W cm−2 while exhibiting stable operation for a continuous duration of 120 h at a constant current of 0.8 A cm−2, with performance remaining optimal. Moreover, SNC-20SZM demonstrates exceptional durability and stability over prolonged durations even in high CO2 atmospheres. An innovative approach for enhancing the development of intermediate-temperature solid oxide fuel cells (IT-SOFCs) involves incorporating SZM in the SNC cathode, thereby augmenting electrochemical performance and narrowing the gap in the thermal expansion coefficient among SOFC modules.

CO2/Cr-tolerance and oxygen reduction reaction of novel high-entropy perovskite cathode for intermediate temperature solid oxide fuel cell

The development and exploration of cathode oxides with outstanding electrocatalytic activity are critical processes aimed at achieving a decrease in the operation temperature of solid oxide fuel cells (SOFC). Herein, a novel high-entropy oxide, La0.2Pr0.2Nd0.2Sm0.2Gd0.2BaCoFeO5+δ (HEP), which incorporates five lanthanide species (La, Pr, Nd, Sm, and Gd) in the A-site of perovskite, has been specifically developed and assessed as selected cathode for intermediate-temperature SOFC. Investigations of phase structure, chemical compatibility, oxygen transport characteristics, oxygen reaction kinetic, thermal expansion, surface chemical state, conductivity, as well as CO2/Cr-durability are thoroughly performed to assess the basic physicochemical properties of the HEP cathodes. The HEP cathode possesses good operational stability, moderate thermal expansion behavior, fast oxygen transport dynamics, and superior chemical compatibility with the electrolyte. At 700 °C, the polarization resistance low to 0.072 Ω cm2 and output power density high to 332.2 mW cm−2 were obtained for the symmetrical and electrolyte-supported single cells. Furthermore, a stable current density is obtained for the single cell operating at 600 °C and 0.5 V for 100 h. Analysis of electrochemical impedance spectra (EIS) and distribution of relaxation time (DRT) data at different oxygen partial pressures reveal that the charge-transfer and oxygen ions ionization processes at intermediate frequencies present a significant limiting step in the rate of the oxygen reduction reaction. However, under realistic utilization conditions, cathodes of cells often endure irreversible performance degradation owing to the Cr deposition from interconnects or CO2 poisoning in air. Hence, the behavior of Cr and CO2 poisoning is also systematically investigated in symmetrical cell measurements; the results confirm that the HEP cathode displays good resistance to Cr and CO2 poisoning. Overall, our findings indicate that the HEP material is regarded as a favored ceramic cathode for SOFC.

In situ construction of A-site high-entropy perovskites with interfacial CeO2 for a high-performance IT-SOFC air-electrode.

Developing an intermediate-temperature solid oxide fuel cell (IT-SOFC) is one of the most promising ways of achieving carbon neutrality, but its air-electrode is restricted by the conflict between the sluggish catalytic activity and durability. Herein, an A-site high-entropy perovskite composite La0.2Ba0.2Sr0.2Ca0.2Ce0.2-xCoO3-δ-xCeO2 (LBSCCC-CeO2) air-electrode material is fabricated via a one-step self-constructing strategy, which shows excellent oxygen reduction activity and stability due to the high-entropy structure and the synergy effect between LBSCCC and interfacial CeO2. This work provides a new way of fabricating high-performance air-electrodes in IT-SOFCs.

Boosting the electrochemical performance of oxygen electrodes via the formation of LSCF-BaCe0.9–xMoxY0.1O3–δ triple conducting composite for solid oxide fuel cells: Part II

This research is the continuation of our previous work, in which we introduced novel proton-conducting electrolytes BaCe0.9–xMoxY0.1O3–δ (BCMxY; x = 0.025, 0.05). In this study, we explore the potential of the proton-conducting BCM0.025Y electrolyte by creating a composite with La0.6Sr0.4Co0.2Fe0.8O3–δ (LSCF) to form triple conducting electrodes for solid oxide fuel cells (SOFC). The formation of the LSCF-BCM0.025Y composite enhances both the three-phase reaction interface length and the concentration of oxygen vacancies, contributing to improved dissociation rates and enhanced oxygen adsorption. The desired characteristics, including density, structure, composition, electrochemical performance, and thermal stability, have been confirmed through a comprehensive set of analyses including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), electrochemical impedance spectroscopy (EIS), and thermogravimetric analysis (TGA) coupled with differential scanning calorimetry (DSC), respectively. The cell configuration of Ni-YSZ | BCZY | LSCF-BCM0.025Y exhibited a remarkable maximum power density (MPD) of 418.7 mW cm−2, which is approximately 29 % higher than that achieved with a typical LSCF cathode (325.6 mW cm−2) at an operating temperature of 600 °C. The outstanding performance and enduring stability of the LSCF-BCM0.025Y composite over a 500 h period demonstrate its potential as a promising cathode material for intermediate-temperature SOFCs.

Ce-doped promotes the phase stability and electrochemical performance of SrCoO3-δ cathode for intermediate-temperature solid oxide fuel cells

The development of cathode with high oxygen reduction reaction (ORR) activity is crucial for intermediate-temperature solid oxide fuel cells (IT-SOFCs). SrCoO3-δ oxides, a mixed ion-electron conductivity (MIEC), are promising cathode materials. However, pure SrCoO3-δ exhibits a hexagonal or rhombohedral structure with poor electrical properties, limiting its application in IT-SOFCs. In this work, high-valence Ce4+ is doped at the A-site of SrCoO3-δ perovskite to improve the phase structural stability and electrochemical activity of SrCoO3-δ. The findings reveal that Ce4+ doping in small amounts significantly advances the conductivity and ORR activity due to enhanced structural stability. Among the series of samples, Sr0.95Ce0.05Co3-δ (SCC005) presents the best electrochemical performance. Moreover, the addition of Ce0.8Gd0.2O2-δ (GDC) further reduces polarization resistance by about ∼7 times. The peak power density of 1.3 W cm−2 is obtained at 750 °C for the SCC05-30%GDC cathode. The results indicate that A-site Ce doping is a promising strategy to enhance the ORR activity of SrCoO3-δ oxides.

High entropy double perovskite cathodes with enhanced activity and operational stability for solid oxide fuel cells

Rare-earth site high entropy double perovskite oxides with different molar ratios have been evaluated as the cathodes for intermediate-temperature solid oxide fuel cells (IT-SOFC). The effect of configuration entropy on crystal structure, electrical conductivity, electrochemical performance and stability are investigated. Our results reveal that the activity of all high entropy oxides show enhanced electrochemical activity. Among them, the equimolar one (HEO) exhibits the highest activity with a low polarization resistance of 0.05 Ω cm2 at 700 °C. Moreover, it exhibits excellent stability in the CO2-containing atmosphere. The enhanced activity and operational stability can be attributed to reduced surface Ba segregation and the formation of active and robust BaCoO3-δ nanoparticles on HEO surface, rather than BaCO3 and Co3O4 phases. This work indicates that configurational entropy engineering is very effective for rational surface composition regulation.

Structural and electrical properties of Gd and W co-doped La2Mo2O9 as electrolyte for IT-SOFCs

In this study, a modified sol-gel method was employed to synthesize Gd and W co-doped La2Mo2O9 (LMX). The impact of Gd and W co-doping on the pristine LMX lattice was examined using X-Ray diffraction, and the local structural parameters were analyzed through Rietveld refinement. The findings indicate that both the pure and co-doped LMX samples possess a cubic structure with a P213 space group. To investigate the electrical performance of the lanthanum molybdate (La2Mo2O9) both in its pure form and when co-doped with Gd and W, electrochemical impedance spectroscopy was conducted. The results demonstrated that co-doping enhances the conductivity of oxy-ions compared to pure LMX. Specifically, La1.7Gd0.3Mo1.7W0.3O9 (LMXG3) exhibited a higher ionic conductivity of approximately 2 x 10−2 Scm−1 at a temperature of 650 °C, surpassing the conductivity of the pure LMX sample and other co-doped LMX samples. This investigation highlights the potential of the Gd and W co-doped LMX system as a solid electrolyte for intermediate-temperature solid oxide fuel cells (IT-SOFCs).

Study of structural, electrical, and electrochemical properties of Sr3-xPrxFe1.8Co0.2O7-δ cathode for IT-SOFCs

Developing new cathode materials for intermediate-temperature solid oxide fuel cells (IT-SOFCs) is still challenging. In this study, co-doped Sr3Fe2O7-δ Ruddlesden-Popper (R-P) (Sr3-xPrxFe1.8Co0.2O7-δ x = (0–0.3)) cathode is synthesized by the polymer complex technique as a cathode for IT-SOFCs. The synthesized powders show a desired tetragonal structure of Sr3-xPrxFe1.8Co0.2O7-δ with an I4/mmm space group. The effect of Pr and Co on the physical, thermal, electrical, and electrochemical properties of the cathodes is investigated. The results reveal that Pr/Co co-doping improves electrochemical properties while increasing the electrical resistivity and average thermal expansion coefficients (TECs). To evaluate the long-term thermal stability of the cathode, they are heated at 800 °C for 100 h in the air, and no contaminant is found. In the optimal amount of Pr and Co (Sr2.7Pr0.3Fe1.8Co0.2O7-δ), area-specific resistance (ASR) of 0.058 Ω.cm2 and maximum output power density of 745 mW/cm2 are obtained at 800 °C. Strong oxygen-reducing reaction (ORR) activity and long-term thermal stability make Sr2.7Pr0.3Fe1.8Co0.2O7-δ an appropriate alternative cathode material for IT-SOFC.

Effects of Bi2O3 doping on structural and electrical properties of Ce0.8Sm0.2O1.9 electrolyte for solid oxide fuel cells

The study investigates the impact of Bi2O3 doping on the crystal structure, density, and ionic conductivity of Ce0.8Sm0.2O1.9, a type of samarium-doped ceria oxide (SDC). The material is intended for use as a solid electrolyte in intermediate temperature solid oxide fuel cells (IT-SOFCs). The SDC-based electrolyte was created using the auto-combustion technique, with various molar ratios of Bi2O3. Phase compositions, microstructure, and ionic conductivity of all ceria ceramics were analysed using XRD, SEM and impedance analyses, respectively. The language is formal, clear, objective, and value-neutral, using high-level, standard language with consistent technical terms. Grammar, spelling, and punctuation are correct. Consistent citation and footnote style are maintained. The samples are single-phase ceramics that crystallise into a cubic fluorite type structure with space group Fm-3 m, as confirmed by the X-ray diffraction pattern. Technical abbreviations are explained. The structure ensures a logical flow of information with causal connections between statements. No filler words or biased language are used. SDC/Bi2O3 composite powders exhibit high sintering activity. The relative density of all samples sintered at 1300 ºC for 5 h was more than 96%, which is higher than that achieved by pure SDC electrolyte sintered at 1400 ºC (94.06%). Electrochemical performance results demonstrate that adding an appropriate amount of Bi2O3 can significantly enhance the conductivity of SDC materials. The SDC-based electrolyte containing 9 mol% of Bi2O3 (SDCB9) demonstrates the maximum conductivity of 43.5 mS·cm−1 at 800 °C, surpassing that of pure SDC which measures 26.86 mS·cm−1.

Experimental study and first-principles calculation of enhanced electrochemical properties of Bi0.7Sr0.3FeO3-δ (BSFO) – La0.8Sr0.2MnO3-δ (LSM) composite cathodes for intermediate-temperature solid oxide fuel cells

In order to enhance the electrochemical performance of cobalt-free Bi0.7Sr0.3FeO3-δ (BSFO) cathodes for intermediate-temperature solid oxide fuel cells (IT-SOFCs), a composite cathode consisting of BSFO and La0.8Sr0.2MnO3-δ (LSM) is developed. The optimized polarization resistance of the composite cathode (0.11 Ω cm2 at 800 °C) is found to be only 61 % that of pure BSFO (0.18 Ω cm2 at 800 °C), indicating a significant improvement in performance. The first-principles calculation indicates that the enhanced electrochemical performance is mainly due to the domain of low oxygen vacancy formation energies of BSFO-LSM-L interfaces (Evac, −3.63 eV) and LSM (Evac, −3.11 eV). The anode-supported single cell of NiO-SDC/SDC/BSFO－LSM shows a peak power density of 825.83 mW cm−2 at 800 °C using wet H2 (∼3 vol% H2O) as fuels and ambient air as oxidants. In addition, the single cell exhibits a good stability at the electric current density 400 mA cm−2 for 50 h measured at 650 °C.

Study on the composite structure of cobalt-free oxides as cathodes for intermediate temperature solid oxide fuel cells (IT-SOFCs)

Summary: Solid Oxide Fuel Cells (SOFCs) represent a promising technology for efficient and clean energy conversion. This study focuses on the design and development of a novel cathode material for SOFCs, specifically exploring the use of a free-cobalt cathode within a composite structure. Investigating the structure of cobalt-free composites of Ba0.5Sr0.5FeO3-δ (BSF) and Ba0.5Sr0.5Fe0.8B0.2O3-δ (B=Cu, Zn) (BSFB) have been prepared and evaluated as cathodes for IT-SOFCs. The solid-state reaction was employed for generating and modifying the composite structure of the model system. The decomposition reaction and the formation of perovskite structure have been observed using thermal gravimetric analysis and X-ray diffraction. The study encompasses experimental procedures, data processing using GSAS software, and the application of the Rietveld method to achieve precise analysis results. Rietveld analysis outcomes offer intricate details about the crystal structure, encompassing crystal unit parameters, and scale factors. The solid-state reaction led to the reduction in the weight of the composite during the heating process. The decomposition reaction of oxides was generated between 650 to 950 oC. The average of total weight loss during the period treatment was achieved up to 18 % and the perovskite phase formed in the composite structure. A single-phase perovskite from a cubic structure with space group Pm-3m was demonstrated by all composite’s models. The lattice parameter and a unit cell volume were obtained from the model system of BSF, BSFC and BSFZ, respectively. This study explores the potential development of SOFCs technology with the hope of making a positive contribution to advancing clean and sustainable energy solutions in the future

Towards sustainable electrochemistry: green synthesis and sintering aid modulations in the development of BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) IT-SOFC electrolytes

In this study, BaZr0.87Y0.1M0.03O3−δ perovskite electrolytes with sintering aids (M = Mn, Co, and Fe) were synthesized by a sustainable approach using spinach powder as a chelating agent and then compared with chemically synthesized BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes for intermediate temperature SOFCs. This is the first example of such a sustainable synthesis of perovskite materials with sintering aids. Structural analysis revealed the presence of a cubic perovskite structure in BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) samples synthesized by both green and conventional chemical methods. No significant secondary phases were observed in the samples synthesized by a sustainable approach. The observed phenomena of plane shift were because of the disparities between ionic radii of the dopants, impurities, and host materials. The surface morphology analysis revealed a denser microstructure for the electrolytes synthesized via green routes due to metallic impurities in the organic chelating agent. The absence of significant impurities was also observed by compositional analysis, while functional groups were identified through Fourier-transform infrared spectroscopy. Conductivity measurements showed that BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes synthesized by oxalic acid have higher conductivities compared to BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes synthesized by the green approach. The button cells employing BaZr0.87Y0.1Co0.03O3−δ electrolytes synthesized by the chemical and green routes achieved peak power densities 344 and 271 mW·cm−2 respectively, suggesting that the novel green route can be applied to synthesize SOFC perovskite materials with minimal environmental impact and without significantly compromising cell performance.

Sr-deficient medium-entropy Sr1-xCo0.5Fe0.2Ti0.1Ta0.1Nb0.1O3-δ cathodes with high Cr tolerance for solid oxide fuel cells

In this work, Sr-deficiency is proposed as an effective strategy to improve the oxygen reduction reaction (ORR) activity and Cr tolerance of medium-entropy Sr1-xCo0.5Fe0.2Ti0.1Ta0.1Nb0.1O3-δ (S1-xCFTTN, x=0–0.15) cathodes for intermediate temperature solid oxide fuel cells (IT-SOFCs). With proper Sr-deficiency, S0.95CFTTN possesses the highest electrical conductivity and fastest oxygen exchange kinetics within tested samples. The optimized cathode yields outstanding ORR activity with a polarization resistance of 0.024 Ω cm2 at 700 °C, much lower than 0.037 Ω cm2 for SCFTTN cathode. Based on these, an anode-supported cell with S0.95CFTTN cathode exhibits a peak power density of 1153.5 mW cm−2 at 800 °C, much higher than that with SCFTTN cathode. Moreover, the S0.95CFTTN cathode displays dramatically enhanced Cr tolerance ability, which is due to the Sr-deficient diminishes surface Sr segregation and subsequent the formation of SrCrO4. Our results indicate appropriate Sr-deficiency is an effective approach to enhance the ORR activity and stability of SOFC cathodes.

Microstructure and electrical conductivity of La10Si6O27–La0.9Sr0.1Ga0.8Mg0.2O2.85 composite electrolytes for SOFCs

Composite ceramic electrolytes with heterostructure have attracted wide attention from the scientific community due to their enhanced conductivity and stability compared with single component electrolytes. Along these lines, in this work, to improve the conductivity of lanthanum silicate, a series of La10Si6O27 (LSO) - La0.9Sr0.1Ga0.8Mg0.2O2.85 (LSGM) electrolytes were developed, which were composed of apatite/perovskite heterostructure. The phase composition, heterogeneous structure, and morphology of the samples were investigated by performing X-ray diffraction (XRD), transmission electron microscopy (TEM) measurements, as well as, field emission scanning electron microscopy (FE-SEM) for in-depth analysis. In addition, the Archimedes method was employed to test the relative density of the samples. X-ray photoelectron spectroscopy (XPS) was used to examine changes in oxygen vacancies at different LSGM contents. Compared with the pure LSO material, the content of oxygen vacancies increases significantly and the conductivity is highest when the LSGM content is 10 %, which indicates that the newly formed oxygen vacancies in the composite LSO-LSGM electrolyte play an important role in improving the ionic conductivity. At 400 °C, the conductivity of 90 wt%LSO:10 wt%LSGM was 3.4 times that of pure LSO, and at 600 °C, the conductivity of 90 wt%LSO:10 wt%LSGM was an order of magnitude higher than that of pure LSO. From the electrochemical impedance spectra (EIS) analysis, it was shown that the small resistance achieved by the grain boundary was the main reason for its excellent performance. Our results provide valuable insights for the design of more composite electrolytes for intermediate-temperature SOFCs.

Characterization of B‐Site Sc‐doped La2Ni1-xScxO4+δ (x=0, 0.05, 0.10, and 0.15) perovskites as cathode materials for IT-SOFCs

Cathode materials play a crucial role in enabling the widespread adoption of intermediate-temperature solid oxide fuel cells (IT-SOFC) for commercial applications. This study utilized the sol-gel method to prepare a range of perovskite oxides, specifically Sc-doped La2Ni1-xScxO4+δ (x = 0, 0.05, 0.10, and 0.15), without the use of cobalt. The investigation focused on making a study of how the introduction of Sc doping affected the thermal stability, electrochemical properties, and structure of cathode materials. XRD, FE-SEM, and electrochemical workstations were subjected to structural characterization and performance testing of materials. The findings indicate that all the prepared materials have a typical Ruddlesden-Popper structure, and an abundance of additional oxygen can be generated in close proximity to the interstitial by incorporating Sc into the cathode of La2Ni1-xScxO4+δ to increase the oxygen vacancy and improve the catalytic activity of ORR. La2Ni0.9Sc0.1O4+δ has the highest oxygen surface exchange kinetics, the dissociative adsorption of oxygen is the rate-limiting step at the cathode. At a temperature of 700 °C, the lowest polarization resistance of La2Ni0.9Sc0.1O4+δ is 0.1298 Ω cm2, while the single cell with La2Ni0.9Sc0.1O4+δ as the cathode achieves an impressive peak power density of 0.462 W cm−2, thus demonstrating exceptional long-term stability. La2Ni0.9Sc0.1O4+δ is expected to be a potential high-performance IT-SOFC cathode material.

Tailoring the electrochemical reduction kinetics of dual-phase BaCe0.5Fe0.5O cathode via incorporating Mo for IT-SOFCs

The BaCe0.5Fe0.5O3-δ (BCF) cathode consists of the ion-electron mixed conducting phase BaCe0.15Fe0.85O3-δ (BCF1585) and the proton-conducting phase BaCe0.85Fe0.15O3-δ (BCF8515). In this paper, the electrochemical performance is improved by incorporating the high valence element Mo into the BCF and applied to intermediate-temperature solid oxide fuel cells (IT-SOFCs). High-temperature X-ray diffraction (HT-XRD) and O2-temperature programmed desorption (O2-TPD) results show that Mo doping enhances the structural stability of BCF. The X-ray photoelectron spectroscopy (XPS) results suggest that the introduction of Mo increases the amount of adsorbed oxygen and thus the oxygen reduction reaction (ORR) catalytic activity. Compared to BCF, the polarization impedance of BaCe0.5Fe0.45Mo0.05O3-δ (BCFM) at 800°C is 0.154 Ω·cm2, a reduction of 22%. Meanwhile, the BCFM output power at 800°C is 778.01 mW·cm-2, an improvement of 32.17%, and maintains a stable current density after 250 h at 0.7 V. The results demonstrate that Mo doping is an effective strategy to enhance the electrochemical performance of BCF.

Hetero-structured composite cathodes by electrospinning with high CO2-poisoning tolerance for solid oxide fuel cells

The sluggish oxygen reduction reaction (ORR) kinetics significantly hinder the development of intermediate temperature solid oxide fuel cells (IT-SOFC). Herein, a heterostructure composite fibers cathode composed of Ba0.9La0.1Co0.7Fe0.2Nb0.1O3-δ and Sm0.2Ce0.8O2-δ (BLCFN-SDC fibers) has been co-synthesized by electrospinning method, which exhibited excellent electrochemical activity, CO2 tolerance and long-term stability. The polarization resistance (Rp) of BLCFN-SDC fibers cathode at 700 °C is only 0.050 Ω cm2, much lower than those of single-phase BLCFN fibers (0.069 Ω cm2) and BLCFN powders (0.073 Ω cm2). Such improvement can be attributed to the extended three-phase boundary (TPB) and more exposed oxygen reduction reaction (ORR) active sites. Besides, the unique fibers structure provides continuous charge transport paths, which improve its conductivity. Furthermore, BLCFN-SDC fibers exhibits excellent CO2 tolerance in high concentration CO2 atmosphere, benefited from the low CO2 adsorption characteristics and stability of SDC. The results suggest that such heterostructure fibers cathode with excellent ORR activity and CO2 durability might provide a novel method to design efficient catalysts for SOFCs and other energy conversion devices.

Influence of K+ substitution on germanium doped strontium silicate (Sr3-3xK3xSi3-3yGe3yO9-δ; 0 ≤ x ≤ 0.20, y=0.1) for application as solid electrolyte

The different alkali metal substitution strategies of the strontium meta-silicate based ion conductors have been enormously cross-examined to synthesize cost-effective novel electrolyte for Intermediate Temperature Solid Oxide Fuel Cells (IT-SOFCs). In the present investigation, crystal structure, phase formation, microstructure, total conductivity and stability of the Potassium and Germanium incorporated Sr3Si3O9 based system, Sr3-3xK3xSi3-3yGe3yO9-δ (0 ≤ x ≤ 0.20, y = 0.1), is examined for their application as solid electrolyte for electrochemical devices such as ITSOFCs. These samples have been made via solid state reaction route. X-ray Rietveld refinement method was used for the structural investigation. Raman and FT-IR spectroscopy were performed to examine the phase formation and absorption of light by the bonds of vibrating molecules to provide molecular characteristics and vibrational modes of the molecules. The X-ray Photoelectron Spectroscopy study was used to validate the characteristic valence states of the constituting elements. Thermo-gravimetric analysis was performed to inspect the thermal stability and weight changes in the compounds during heating process. In the SEM and EDS mapping, an amorphous phase of K2Si2O5 can be visualized which seems to segregate along grain boundaries and this amorphous complexion augmented with K+ dopant concentration. AC Electrical impedance spectroscopy studies suggest that the ionic conduction in Sr3-3xK3xSi3-3yGe3yO9-δ could be from the oxide ions along with mobility of K+ ions of the glassy phase. In this study, we also tried to get the optimal doping condition with compositions to minimize numerous concern of the system.

Surface modulated B-site doping of PrBa0.5Sr0.5Co2-xFexO5+δ as highly efficient cathode for intermediate-temperature solid oxide fuel cells

Layered perovskite oxides (PrBaCo2O5+δ) have gained widespread interest as promising electrodes in intermediate-temperature solid oxide fuel cells (IT-SOFCs) because of their excellent oxygen diffusion and transport performance. However, it remains a great challenge to simultaneously realize thermal match and sufficient operational stability in existing IT-SOFCs. Herein, the layered perovskite PrBa0.5Sr0.5Co2-xFexO5+δ (PBSCFx) with strong oxygen reduction reaction (ORR) activity in half-cell and high power density in single cell was designed by partial substitution of Co with Fe. A systematic and comprehensive elaboration on the composition-structure-property relationships of PBSCFx was proposed. Furthermore, the complex electrochemical behavior of the single cell was investigated using equivalent circuit method (ECM) and distribution of relaxation time (DRT). Impressively, the polarization impedance of PBSCF05 (x = 0.5) is only 0.037 Ω·cm2 (T = 750 °C). The single cell with PBSCF05-GDC as the cathode can reach the maximum power density of 0.996 W/cm2 (T = 800 °C), and exhibits good stability in 216 h of long-term operation (T = 750 °C). The superior electrochemical performance of PBSCF05 is mainly attributed to the reduction of high frequency and intermediate frequency polarization resistance, which corresponds to the enhanced transfer process of oxygen ions, oxygen surface exchange and charge transfer process. This work highlights a simple B-site doping strategy to achieve the thermal match in IT-SOFCs, and furthermore, it expands the opportunities for effective utilization of ECM and DRT technology in the high-performance of IT-SOFCs.

Development of conducting Bi0.5Sr0.5FeO3–δ-Gd0.1Ce0.9O2–δ composite cathodes for IT-SOFCs

Decreasing the working temperature of solid oxide fuel cells (SOFCs) to 400 °C–600 °C is a primary concern for current fuel cell research. Unfortunately decrease in operating temperatures leads to increase in cathode polarization, which deteriorates electrochemical activity of the cathode for oxygen reduction reaction (ORR). Consequently, the search of new cathode materialsis one of the critical bottle-neck towards the development of intermediate-temperature SOFCs (IT-SOFCs). In this study, we have successfully synthesized Bi0.5Sr0.5FeO3-δ and Bi0.5Sr0.5FeO3-δ-Gd0.1Ce0.9O2-δ((1-x) BSFO-xGDC) composite cathodes with varying compositions (x = 50, 40, 30, and 20wt%). The crystal structure, microstructure, electrochemical properties and performance stability of these composite cathodes have been comprehensively evaluated using techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). Our results demonstrate that the introduction of Gd0.1Ce0.9O2-δ( GDC) has a significant impact on the electrochemical performance of the composite cathodes. Among the different compositions studied, the cathode with a composition of x = 70 wt% exhibits particularly promising electrochemical properties. The electrode resistance polarization of 70BiSFO-30GDC is 0.39 Ωcm2 and 0.8 Ωcm2 for symmetrical and half-cell at 600 °C. The preliminary results of this study reveal that the 70BiSFO-30GDC composite cathode demonstrates remarkable ORR activity. Further investigations and comprehensive analyses are warranted to validate and explore the full potential of the 70BiSFO-30GDC composite cathode in the context of SOFC applications.