1. Introduction
Perovskite-related materials, particularly transition metal oxides, have garnered significant attention due to their versatile structural properties and wide range of potential applications in fields such as catalysis, solid oxide fuel cells, electrodes and gas sensors [1]-[4]. Among these materials, A2BB’O6-δ-type double perovskites have shown promise due to their tunable oxygen deficiency, which can enhance their ionic conductivity and catalytic properties [5]. One material of growing interest is Ca2FeGaO6-δ, a compound where gallium (Ga) and iron (Fe) occupy the B-sites, forming a unique framework capable of accommodating varying oxygen vacancies (δ) [6].
The characterization of such materials is essential for understanding their structural and electrochemical properties. Scanning Electron Microscopy (SEM) is a powerful technique for investigating the surface morphology and microstructural details at the submicron scale. In the case of Ca2FeGaO6-δ, SEM analysis provides critical insights into grain size, texture, and porosity, all of which influence the material’s overall performance in technological applications.
This study presents a detailed SEM analysis of Ca2FeGaO6-δ, focusing on its microstructure and the impact of oxygen vacancies on its morphology. By correlating the SEM data with the material’s composition and structural characteristics, we aim to better understand the material’s potential for high-performance applications.
2. Experimental
Solid-state synthesis method was used to synthesize the material, Ca2FeGaO6-δ. The powders of the precursor compounds, CaCO3 (Alfa Aesar, 99.95%), Fe2O3 (Alfa Aesar, 99.998%) and Ga2O3 (Sigma Aldrich, 99.99%) were mixed in the stoichiometric proportions and ground together using an agate mortar and pestle, pressed into a pellet, and calcined in air at 1000˚C for 24 h in MTI muffle furnace. The samples were then reground and sintered at 1200˚C for 24 h in the same environment, followed by slow cooling. The heating and cooling rates were 100˚C/h. The phase purity and structure of the polycrystalline samples were determined by powder X-ray diffraction (XRD) at room temperature using Cu Kα1 radiation (λ = 1.54056 Å). The GSAS software [7] and EXPGUI interface [8] were used for Rietveld refinements [9]. The microstructures were studied using high-resolution field emission scanning electron microscopy (JEOL-SEM).
3. Crystal Structure of Ca2FeGaO6-δ
The oxygen-deficient perovskite Ca2FeGaO6-δ crystallizes in the orthorhombic Pcmn space group [6]. The refined XRD profile of Ca2FeGaO6-δ is shown in Figure 1. The structure is derived from the typical ABO3 perovskite framework [10], where Ca2+ ions occupy the A-site, while Fe3⁺ and Ga3⁺ cations are distributed over the B-site. The oxygen sublattice is incomplete due to the oxygen deficiency, denoted by δ, leading to potential oxygen vacancies that affect the material’s electrical and ionic conductivity.
In this orthorhombic structure, the Fe3+ and Ga3+ cations are octahedrally coordinated by oxygen, forming corner-sharing FeO6 and GaO6 octahedra. The partial occupancy of oxygen sites due to δ introduces distortions in the octahedra, causing deviations from ideal octahedral symmetry. These distortions manifest as tilting and rotation of the octahedra, which are characteristic of oxygen-deficient perovskites and contribute to the overall structural complexity.
The Ca2+ ions are coordinated by oxygen in an irregular geometry, positioned in the large interstitial sites between the octahedral units. The oxygen vacancies distributed throughout the structure, can significantly influence both the ionic conductivity and the structural stability of the material.
Figure 1. Powder X-ray diffraction data of Ca2FeGaO6-δ. The black crosses, red lines, green vertical lines, and blue solid lines represent the raw data, the model, Bragg peak positions, and plot differences.
The Pc symmetry results in alternating tilts of the FeO6 and GaO6 octahedra along the c-axis, while distortions along the a and b axes are accommodated through shifts in the positions of the oxygen anions. This tilting system and the oxygen-deficient nature of the material are expected to contribute to unique physical properties, including mixed ionic-electronic conductivity and potential thermoelectric or catalytic behavior.
The unit cell dimensions and atomic coordinates, refined through X-ray diffraction (XRD) studies, reveal that the structure maintains orthorhombic symmetry, though subtle variations in bond lengths and angles arise from the presence of oxygen vacancies and the different ionic radii of Fe3⁺ and Ga3⁺. These structural features are key to understanding the material’s physical properties, including its electrical conductivity and potential applications in energy-related fields.
4. Scanning Electron Microscopy (SEM) Analysis
The SEM analysis of the oxygen-deficient brownmillerite, Ca2FeGaO6-δ reveals crucial insights into the material’s surface morphology, particle size distribution, and microstructural characteristics, which are important for understanding its physical and chemical behavior.
The SEM images display a well-defined polycrystalline structure, as shown in Figure 2, with grains ranging from sub-micron to a few microns in size. These grains exhibit an irregular shape, often angular or faceted, which is typical of perovskite-derived materials synthesized through solid-state reactions. The grain size ranges from 6.6 μm to 31.74 μm width dimension, as seen in the top left SEM image. The length of the grains ranges from very small to 33.3 μm. The presence of grain boundaries between the crystallites is evident, and these interfaces could play a significant role in ionic and electronic transport within the material. Additionally, some regions show signs of intergranular porosity, likely a result of oxygen vacancies within the brownmillerite lattice.
At higher magnifications, the microstructure exhibits distinct surface features, such as terrace-like step formations, which are indicative of the layered nature of brownmillerite structures. These terraces arise from the alternating octahedral and tetrahedral layers within the material and contribute to the complex grain morphology. The rough texture observed on the surface may be linked to oxygen deficiency (δ), leading to defects and slight lattice distortions that affect surface stability.
Further analysis of the microstructure highlights the presence of micropores and small voids, which are distributed across the grain surfaces. These pores are likely associated with the oxygen vacancy ordering within the brownmillerite phase, contributing to the material’s low density and potentially enhancing its catalytic or ion transport properties. The pore distribution may also suggest incomplete densification during the synthesis process, or it could be a result of the loss of oxygen during cooling.
Figure 2. SEM images of Ca2FeGaO6-δ. Left: ×500 magnification, and right: ×2000 magnification.
Energy-dispersive X-ray spectroscopy (EDS) coupled with SEM confirms the elemental composition of the material, showing a uniform distribution of Ca, Fe, Ga, and O across the sample, as displayed in Figure 3. The elemental mapping reveals no significant segregation of iron or gallium, suggesting homogeneity within the grains. The oxygen content appears to be slightly reduced in certain regions, further supporting the presence of ordered oxygen vacancies and structural inhomogeneities that contribute to the brownmillerite behavior of Ca2FeGaO6-δ.
Porosity decreases a material’s thermal conductivity or its ability to conduct heat. This is because porosity reduces the number of direct paths for heat conduction, increases thermal resistance, and reduces solid-to-solid contact [11]. The conductivity of a material is determined by how easily electrons can move through it. Collisions between electrons and atoms in the material slow down the electrons and increase the material’s resistivity. Materials with higher conductivity allow electrons to move through more easily, resulting in fewer collisions [11].
The overall surface morphology observed in SEM supports the notion that the microstructural features, including grain size, porosity, and surface roughness, may directly influence the material’s electrochemical properties, such as ionic conductivity and catalytic activity. The porosity, in particular, could enhance gas diffusion in catalytic applications, while the grain boundaries may serve as pathways for ionic conduction in energy storage devices.
Figure 3. SEM images of Ca2FeGaO6-δ for elemental mapping.
5. Conclusion
In conclusion, the SEM analysis of the oxygen-deficient brownmillerite Ca2FeGaO6-δ has provided key insights into the material’s microstructural characteristics, including its irregular grain morphology, significant porosity, and the presence of oxygen vacancies. These structural features are strongly linked to the functional properties of the material, particularly its potential in applications requiring catalytic activity, ionic conductivity, and gas diffusion. The non-uniform grain growth and porous structure suggest that oxygen vacancies play a pivotal role in shaping the material’s performance, potentially enhancing its reactivity and transport properties. These findings contribute to a deeper understanding of the relationship between the microstructure and the functional behavior of Ca2FeGaO6-δ, paving the way for further investigations into optimizing its properties for practical applications in energy storage, sensors, and catalytic technologies. Future studies may focus on refining the synthesis process to control grain size and oxygen vacancy distribution, ultimately improving the material’s performance in advanced technological applications.
Acknowledgements
This work is partly supported by the National Science Foundation Tribal College and University Program Instructional Capacity Excellence in TCUP Institutions (ICE-TI) grant award # 2225648. A part of this work is supported by NSF TCUP Tribal Enterprise Advancement Center grant no. HRD 1839895. A part of the work is supported by AIHEC-coordinated NASA TCU Building Bridges, Grant Number 80NSSC24M0025. Additional support for the work came from ND EPSCOR STEM equipment grants. Permission was granted by the United Tribes Technical Colleges (UTTC) Environmental Science Department to publish this information. The views expressed are those of the authors and do not necessarily represent those of United Tribes Technical College.