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@article{ad3dd2aa99d0443b841a7a8deb1e71a6,
title = "Thermodynamics of gaseous strontium and calcium cerates studied by Knudsen effusion mass spectrometry and estimation of relative electron ionization cross-section for CeO2(g)",
abstract = "Rationale: Ceria-based systems are of great interest because of their unique properties. Such systems may be used as anode materials for SOFCs or in oxygen sensors. The exploitation of these materials often requires high temperatures. In such conditions, the partial or complete evaporation of materials is possible. Therefore, knowledge of the values of partial pressures and thermodynamic properties is essential to predict and/or prevent possible consequences and accidents. Methods: Knudsen effusion mass spectrometry was used to determine partial pressures of vapor species over the SrO–CeO2 and CaO-CeO2 systems. Measurements of partial pressures were performed with a MS-1301 mass spectrometer. Vaporization was carried out using molybdenum or tungsten effusion cells. A theoretical study of gaseous strontium and calcium cerates was performed by several quantum chemical methods: density functional theory (DFT) M06, DFT PBE0, and MP2. Results: The minimum value of relative electron ionization cross-section for CeO2 was estimated. In the temperature range of 2218–2249 K above the SrO-CeO2 system and of 2128–2208 K above the CaO-CeO2 system, gaseous M, MO, MO, CeO2, O, O2 and MCeO3 (M = Sr, Ca) were found. Energetically favorable structures of gaseous SrCeO3 and CaCeO3 were found, and vibrational frequencies were evaluated in the “rigid rotor-harmonic oscillator” approximation. On the basis of the equilibrium constants of gaseous reaction MO + CeO2 = MCeO3, the standard formation enthalpy of gaseous SrCeO3 (−913 ± 26 kJ/mol) and of gaseous CaCeO3 (−917 ± 26 kJ/mol) at 298 K were determined. Conclusions: The estimated value of relative electron ionization cross-section for CeO2 is in agreement with the general rule applicable for dioxides. The stability of SrCeO3 and CaCeO3 gaseous species was confirmed by KEMS. Gas-phase reactions involving gaseous SrO (CaO) and CeO2 with gaseous SrCeO3(CaCeO3) were studied. Enthalpy of formation reaction of gaseous SrCeO3(CaCeO3) from gaseous SrO (CaO) were evaluated theoretically, and the obtained value is in agreement with the experimental one.",
keywords = "KEMS, cerates, cerium dioxide (ceria)",
author = "Шугуров, {Сергей Михайлович} and Лопатин, {Сергей Игоревич} and Жинкина, {Ольга Антоновна} and Панин, {Андрей Иванович} and Панина, {Наталья Сергеевна}",
note = "Shugurov SM, Lopatin SI, Zhinkina OA, Panin AI, Panina NS. Thermodynamics of gaseous strontium and calcium cerates studied by Knudsen effusion mass spectrometry and estimation of relative electron ionization cross-section for CeO2(g). Rapid Commun Mass Spectrom. 2024;38(21):e9894. doi:10.1002/rcm.9894",
year = "2024",
month = nov,
day = "15",
doi = "10.1002/rcm.9894",
language = "English",
volume = "38",
journal = "Rapid Communications in Mass Spectrometry",
issn = "0951-4198",
publisher = "Wiley-Blackwell",
number = "21",

}

RIS

TY - JOUR

T1 - Thermodynamics of gaseous strontium and calcium cerates studied by Knudsen effusion mass spectrometry and estimation of relative electron ionization cross-section for CeO2(g)

AU - Шугуров, Сергей Михайлович

AU - Лопатин, Сергей Игоревич

AU - Жинкина, Ольга Антоновна

AU - Панин, Андрей Иванович

AU - Панина, Наталья Сергеевна

N1 - Shugurov SM, Lopatin SI, Zhinkina OA, Panin AI, Panina NS. Thermodynamics of gaseous strontium and calcium cerates studied by Knudsen effusion mass spectrometry and estimation of relative electron ionization cross-section for CeO2(g). Rapid Commun Mass Spectrom. 2024;38(21):e9894. doi:10.1002/rcm.9894

PY - 2024/11/15

Y1 - 2024/11/15

N2 - Rationale: Ceria-based systems are of great interest because of their unique properties. Such systems may be used as anode materials for SOFCs or in oxygen sensors. The exploitation of these materials often requires high temperatures. In such conditions, the partial or complete evaporation of materials is possible. Therefore, knowledge of the values of partial pressures and thermodynamic properties is essential to predict and/or prevent possible consequences and accidents. Methods: Knudsen effusion mass spectrometry was used to determine partial pressures of vapor species over the SrO–CeO2 and CaO-CeO2 systems. Measurements of partial pressures were performed with a MS-1301 mass spectrometer. Vaporization was carried out using molybdenum or tungsten effusion cells. A theoretical study of gaseous strontium and calcium cerates was performed by several quantum chemical methods: density functional theory (DFT) M06, DFT PBE0, and MP2. Results: The minimum value of relative electron ionization cross-section for CeO2 was estimated. In the temperature range of 2218–2249 K above the SrO-CeO2 system and of 2128–2208 K above the CaO-CeO2 system, gaseous M, MO, MO, CeO2, O, O2 and MCeO3 (M = Sr, Ca) were found. Energetically favorable structures of gaseous SrCeO3 and CaCeO3 were found, and vibrational frequencies were evaluated in the “rigid rotor-harmonic oscillator” approximation. On the basis of the equilibrium constants of gaseous reaction MO + CeO2 = MCeO3, the standard formation enthalpy of gaseous SrCeO3 (−913 ± 26 kJ/mol) and of gaseous CaCeO3 (−917 ± 26 kJ/mol) at 298 K were determined. Conclusions: The estimated value of relative electron ionization cross-section for CeO2 is in agreement with the general rule applicable for dioxides. The stability of SrCeO3 and CaCeO3 gaseous species was confirmed by KEMS. Gas-phase reactions involving gaseous SrO (CaO) and CeO2 with gaseous SrCeO3(CaCeO3) were studied. Enthalpy of formation reaction of gaseous SrCeO3(CaCeO3) from gaseous SrO (CaO) were evaluated theoretically, and the obtained value is in agreement with the experimental one.

AB - Rationale: Ceria-based systems are of great interest because of their unique properties. Such systems may be used as anode materials for SOFCs or in oxygen sensors. The exploitation of these materials often requires high temperatures. In such conditions, the partial or complete evaporation of materials is possible. Therefore, knowledge of the values of partial pressures and thermodynamic properties is essential to predict and/or prevent possible consequences and accidents. Methods: Knudsen effusion mass spectrometry was used to determine partial pressures of vapor species over the SrO–CeO2 and CaO-CeO2 systems. Measurements of partial pressures were performed with a MS-1301 mass spectrometer. Vaporization was carried out using molybdenum or tungsten effusion cells. A theoretical study of gaseous strontium and calcium cerates was performed by several quantum chemical methods: density functional theory (DFT) M06, DFT PBE0, and MP2. Results: The minimum value of relative electron ionization cross-section for CeO2 was estimated. In the temperature range of 2218–2249 K above the SrO-CeO2 system and of 2128–2208 K above the CaO-CeO2 system, gaseous M, MO, MO, CeO2, O, O2 and MCeO3 (M = Sr, Ca) were found. Energetically favorable structures of gaseous SrCeO3 and CaCeO3 were found, and vibrational frequencies were evaluated in the “rigid rotor-harmonic oscillator” approximation. On the basis of the equilibrium constants of gaseous reaction MO + CeO2 = MCeO3, the standard formation enthalpy of gaseous SrCeO3 (−913 ± 26 kJ/mol) and of gaseous CaCeO3 (−917 ± 26 kJ/mol) at 298 K were determined. Conclusions: The estimated value of relative electron ionization cross-section for CeO2 is in agreement with the general rule applicable for dioxides. The stability of SrCeO3 and CaCeO3 gaseous species was confirmed by KEMS. Gas-phase reactions involving gaseous SrO (CaO) and CeO2 with gaseous SrCeO3(CaCeO3) were studied. Enthalpy of formation reaction of gaseous SrCeO3(CaCeO3) from gaseous SrO (CaO) were evaluated theoretically, and the obtained value is in agreement with the experimental one.

KW - KEMS

KW - cerates

KW - cerium dioxide (ceria)

UR - https://www.mendeley.com/catalogue/5e86fba7-e0a8-3982-aabe-96cbe3c212f5/

U2 - 10.1002/rcm.9894

DO - 10.1002/rcm.9894

M3 - Article

VL - 38

JO - Rapid Communications in Mass Spectrometry

JF - Rapid Communications in Mass Spectrometry

SN - 0951-4198

IS - 21

M1 - e9894

ER -

ID: 124124377