TY - JOUR
T1 - Reducing the chemical expansion coefficient in ceria by addition of zirconia
AU - Bishop, S. R.
AU - Marrocchelli, D.
AU - Fang, W.
AU - Amezawa, K.
AU - Yashiro, K.
AU - Watson, G. W.
PY - 2013/4
Y1 - 2013/4
N2 - For the first time, the role of isovalent Zr substitution in cerium oxide on the non-stoichiometry induced dilation (chemical expansion) was investigated. Chemical expansion was derived experimentally using HTXRD, dilatometry, and TGA measurements on Pr0.1Zr0.4Ce0.5O 1.95-δ and computationally with DFT calculations on Zr 0.5Ce0.5O2-δ. Though Zr was found to increase the reducibility and the corresponding chemical expansion of ceria in the studied range, the relationship between chemical expansion and non-stoichiometry (the chemical expansion coefficient) was significantly smaller (54% less) than that observed in ceria, and consistent with predictions from the authors' previous work. The origin of the reduced chemical expansion coefficient, associated with a larger contraction of the lattice around oxygen vacancies, is explained using DFT calculations and corroborated with prior investigations of enhanced reducibility of ceria-zirconia. Additionally, implications of this discovery for solid oxide fuel cells and heterogeneous catalyst systems are also discussed.
AB - For the first time, the role of isovalent Zr substitution in cerium oxide on the non-stoichiometry induced dilation (chemical expansion) was investigated. Chemical expansion was derived experimentally using HTXRD, dilatometry, and TGA measurements on Pr0.1Zr0.4Ce0.5O 1.95-δ and computationally with DFT calculations on Zr 0.5Ce0.5O2-δ. Though Zr was found to increase the reducibility and the corresponding chemical expansion of ceria in the studied range, the relationship between chemical expansion and non-stoichiometry (the chemical expansion coefficient) was significantly smaller (54% less) than that observed in ceria, and consistent with predictions from the authors' previous work. The origin of the reduced chemical expansion coefficient, associated with a larger contraction of the lattice around oxygen vacancies, is explained using DFT calculations and corroborated with prior investigations of enhanced reducibility of ceria-zirconia. Additionally, implications of this discovery for solid oxide fuel cells and heterogeneous catalyst systems are also discussed.
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U2 - 10.1039/c3ee23917a
DO - 10.1039/c3ee23917a
M3 - Article
AN - SCOPUS:84875659290
SN - 1754-5692
VL - 6
SP - 1142
EP - 1146
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 4
ER -