scholarly journals High Pressure X-ray Diffraction as a Tool for Designing Doped Ceria Thin Films Electrolytes

Coatings ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 724
Author(s):  
Sara Massardo ◽  
Alessandro Cingolani ◽  
Cristina Artini

Rare earth-doped ceria thin films are currently thoroughly studied to be used in miniaturized solid oxide cells, memristive devices and gas sensors. The employment in such different application fields derives from the most remarkable property of this material, namely ionic conductivity, occurring through the mobility of oxygen ions above a certain threshold temperature. This feature is in turn limited by the association of defects, which hinders the movement of ions through the lattice. In addition to these issues, ionic conductivity in thin films is dominated by the presence of the film/substrate interface, where a strain can arise as a consequence of lattice mismatch. A tensile strain, in particular, when not released through the occurrence of dislocations, enhances ionic conduction through the reduction of activation energy. Within this complex framework, high pressure X-ray diffraction investigations performed on the bulk material are of great help in estimating the bulk modulus of the material, and hence its compressibility, namely its tolerance toward the application of a compressive/tensile stress. In this review, an overview is given about the correlation between structure and transport properties in rare earth-doped ceria films, and the role of high pressure X-ray diffraction studies in the selection of the most proper compositions for the design of thin films.

1999 ◽  
Author(s):  
Ravhi S. Kumar ◽  
A. Sekar ◽  
N. Victor Jaya ◽  
S. Natarajan

2014 ◽  
Vol 1033-1034 ◽  
pp. 1235-1238
Author(s):  
Tao Bai ◽  
Shi Gen Zhu

Rare earth doped titaniumdioxide (TiO2) thin films (rare earth-doped TiO2) have been successfully prepared on a glass substrate by a sol–gel route. After the rare earth-doped TiO2thin films were calcined at 773K for 1h, the effect of rare earth-doping on the properties were investigated using X-ray diffraction (XRD), scanning electronmicroscopy (SEM), ultraviolet–visible spectroscopy and thermogravimetric techniques (TG/DTG). The XRD results showed that rare earth-doped TiO2thin films contained only a single crystalline phase of anatase TiO2after calcining at 773K for 1h. SEM micrographs showed that rare earth-doped TiO2thin films have smooth surfaces containing granular nanocrystallines and are without cracks. The UV–vis absorption spectra showed that the absorption of the rare earth-doped TiO2thin films has a red-shift. From ambient to 1273K, it is about 12% of mass loss because of the volatilizing of water and organic and the phase transformation.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Michael Zoller ◽  
Hubert Huppertz

AbstractThe rare earth oxoborates REB5O8(OH)2 (RE = Ho, Er, Tm) were synthesized in a Walker-type multianvil apparatus at a pressure of 2.5 GPa and a temperature of 673 K. Single-crystal X-ray diffraction data provided the basis for the structure solution and refinement. The compounds crystallize in the monoclinic space group C2 (no. 5) and are composed of a layer-like structure containing dreier and sechser rings of corner sharing [BO4]5− tetrahedra. The rare earth metal cations are coordinated between two adjacent sechser rings. Further characterization was performed utilizing IR spectroscopy.


2013 ◽  
Vol 710 ◽  
pp. 170-173
Author(s):  
Lian Ping Chen ◽  
Yuan Hong Gao

It is hardly possible to obtain rare earth doped CaWO4thin films directly through electrochemical techniques. A two-step method has been proposed to synthesize CaWO4:(Eu3+,Tb3+) thin films at room temperature. X-ray diffraction, energy dispersive X-ray analysis, spectrophotometer were used to characterize their phase, composition and luminescent properties. Results reveal that (Eu3+,Tb3+)-doped CaWO4films have a tetragonal phase. When the ratio of n (Eu)/n (Tb) in the solution is up to 3:1, CaWO4:(Eu3+,Tb3+) thin film will be enriched with Tb element; on the contrary, when the ratio in the solution is lower than 1:4, CaWO4:(Eu3+,Tb3+) thin film will be enriched with Eu element. Under the excitation of 242 nm, sharp emission peaks at 612, 543, 489 and 589 nm have been observed for CaWO4:(Eu3+,Tb3+) thin films.


2008 ◽  
Vol 1122 ◽  
Author(s):  
Gianguido Baldinozzi ◽  
David Simeone ◽  
Dominique Gosset ◽  
Mickael Dollé ◽  
Georgette Petot-Ervas

AbstractWe have synthesized Gd-doped ceria polycrystalline samples (5, 10, 15 %mol), having relative densities exceeding 95% and grain sizes between 30 and 160 nm after axial hot pressing (750 °C, 250 MPa). The samples were prepared by sintering nanopowders obtained by sol-gel chemistry methods having a very narrow size distribution centered at about 16 nm. SEM and X-ray diffraction were performed to characterize the sample microstructures and to assess their structures. We report ionic conductivity measurements using impedance spectroscopy. It is important to investigate the properties of these systems with sub-micrometric grains and as a function of their composition. Therefore, samples having micrometric and nanometric grain sizes (and different Gd content) were studied. Evidence of Gd segregation near the grain boundaries is given and the impact on the ionic conductivity, as a function of the grain size and Gd composition, is discussed and compared to microcrystalline samples.


Coatings ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 432 ◽  
Author(s):  
Nursultan Kainbayev ◽  
Mantas Sriubas ◽  
Darius Virbukas ◽  
Zivile Rutkuniene ◽  
Kristina Bockute ◽  
...  

Samarium-doped ceria (SDC) and gadolinium-doped ceria (GDC) thin films were formed by e-beam vapor deposition on SiO2 substrate, changing the deposition rate and substrate temperature during the deposition. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-Ray spectrometry (EDS) were employed in order to investigate the structure ad morphology of the films. A single Raman peak describing the structure of undoped CeO2 was observed at a frequency of 466 cm−1. Doping of cerium oxide with rare-earth elements shifted the peak to lower frequencies (for Sm—462 cm−1). This shift occurs due to the increased number of oxygen vacancies in doped cerium oxide and it depends on the size and concentration factor of the dopant. It was found that wavenumbers and their intensity differed for the investigated samples, even though the peaks resembled each other in shape. The indicated bands for doped ceria originated as a result of the Raman regime (F2g) of fluorite dioxide associated with the space group (Fm3m). The observed peak‘s position shifting to a lower frequency range demonstrates the symmetric vibrations of oxygen ions around Ce4+ ions in octahedra CeO8. Raman shift to the lower frequencies for the doped samples has two reasons: an increase in oxygen vacancies caused by doping cerium oxide with rare-earth materials and the size factor, i.e., the change in frequency Δω associated with the change in the lattice constant Δa.


2000 ◽  
Vol 658 ◽  
Author(s):  
A. Morata-Orrantia ◽  
S. García-Martín ◽  
E. Morán ◽  
U. Amador ◽  
M. A. Alario-Franco

ABSTRACTThe lithium ion conducting properties of materials of composition La0.58Li0.26TiO3, Nd0.58Li0.26TiO3, La0.67Li0.25Ti0.75Al0.25O3 and La0.29Li0.12NbO3 have been compared in relation with their microstructure. All the oxides have powder X-ray diffraction patterns characteristic of a perovskite-related structure with lattice parameters a∼√2ap, b∼√2ap, c∼2ap (p refers to cubic perovskite). However, some important differences are observed in their microstructure by SAED and HRTEM. Ordering between vacancies, Li+ and La3+ or Nd3+ and twinning of the NbO6 or TiO6 octahedra tilting system are shown in La0.29Li0.12NbO3 and Nd0.58Li0.26TiO3, which are the materials having a lower ionic conductivity. The La0.58Li0.26TiO3 and La0.67Li0.25Ti0.75Al0.25O3 oxides do not show ordering between cations.


2012 ◽  
Vol 531-532 ◽  
pp. 204-207
Author(s):  
Lian Ping Chen ◽  
Yuan Hong Gao

It is hardly possible to obtain rare earth doped CaWO4thin films directly through electrochemical techniques. A two-step method has been proposed to synthesize Tb3+-doped CaWO4thin films. X-ray diffraction, energy dispersive X-ray analysis, spectrophotometer were used to characterize their phase, composition and luminescent properties. Results reveal that Tb3+-doped CaWO4films have a tetragonal phase. The ratio of n(Tb)/[n(Ca)+n(Tb)+n(Na)] decreases with the increase of pH value of TbCl3solutions. When the pH value (adjusted by NaOH) is higher than 5, Na element has been detected in CaWO4:Tb3+thin films. Based on the analysis on the composition and luminescence, it can be concluded that the pH value of TbCl3solutions must be no higher than 9.1, otherwise, no Tb3+-doped CaWO4thin films can be obtained. Under the excitation of 237 nm, sharp emission peaks at 543 and 489 nm have been observed for Tb3+-doped CaWO4:Tb3+thin films.


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