High‐Temperature Proton Conduction in LaSbO4

Lanthanum orthoantimonate was synthesized using a solid‐state synthesis method. To enhance the possible protonic conductivity, samples with the addition of 1 mol % Ca in La‐site were also prepared. The structure was studied by the means of X‐ray diffraction, which showed that both specimens were sin...

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Veröffentlicht in:Chemistry : a European journal 2021-03, Vol.27 (17), p.5393-5398
Hauptverfasser: Winiarz, Piotr, Dzierzgowski, Kacper, Mielewczyk‐Gryń, Aleksandra, Gazda, Maria, Wachowski, Sebastian
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Sprache:eng
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Zusammenfassung:Lanthanum orthoantimonate was synthesized using a solid‐state synthesis method. To enhance the possible protonic conductivity, samples with the addition of 1 mol % Ca in La‐site were also prepared. The structure was studied by the means of X‐ray diffraction, which showed that both specimens were single phase. The materials crystallized in the space group P21/n. Dilatometry revealed that the material expanded non‐linearly with the temperature. The nature of this deviation is unknown; however, the calculated linear fraction thermal expansion coefficient was 9.56×10−6 K−1. Electrical properties studies showed that the material is a proton conductor in oxidizing conditions, which was confirmed both by temperature studies in wet in dry air, but also by the H/D isotope exchange experiment. The conductivity was rather modest, peaking at the order of 10−6 S cm−1 at 800 °C, but this could be further improved by microstructure and doping optimization. This is the first time protonic conductivity in lanthanum orthoantimonates is reported. Lanthanum orthoantimonate is synthesized using a solid‐state synthesis method. To enhance the possible protonic conductivity, samples with the addition of 1 mol % Ca in La‐site are also prepared and characterized by XRD. Dilatometry reveals that the material expands non‐linearly with the temperature, and electrical properties studies show that the material is a proton conductor in oxidizing conditions.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.202004561