Van Vleck paramagnetism in undoped and Lu-doped bulk ceria

Maxim Varenik, Xiao Dong Zhang, Gregory Leitus, Nimrod Yavo, Raanan Carmieli, Ellen Wachtel, Xin Guo, Igor Lubomirsky

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The magnetic properties of undoped, bulk CeO2 are not fully understood. In contrast to nanocrystalline ceria that exhibits paramagnetism attributed to Ce3+ at grain surfaces, bulk ceria is weakly paramagnetic, despite the absence of magnetic ions. In the present work, the magnetic susceptibility of bulk ceria ceramics doped with Lu3+, which has neither spin nor orbital angular momentum, was measured in order to assess the relative contributions of the crystal lattice, residual Ce3+ and oxygen vacancies to the overall bulk magnetization. We observed a magnetic response consisting of two parts: temperature independent (5-300 K) magnetic susceptibility, and Curie-Weiss paramagnetism. The temperature independent susceptibility decreases linearly with Lu content, and becomes diamagnetic at 30 mol% Lu. The Curie-Weiss magnetism visible at low temperatures was identified as resulting from a few ppm of Fe contaminant. However, Fe contamination does not contribute to the temperature independent paramagnetism. No contribution from Ce3+ could be detected. The fact that the magnetization decreases with Lu content, even though the concentration of oxygen vacancies, and the lattice defects associated with them, increases, indicates that neither is coupled to the magnetic field. Weak, temperature-independent paramagnetism in non-metals is usually attributed to a second order, Van Vleck-type magnetization. However, Van Vleck paramagnetism requires that the population of the first excited state be constant within the range of temperatures investigated. We discuss possible modifications of the large band gap electronic structure of undoped ceria which could account for our observations.

Original languageEnglish
Pages (from-to)27019-27024
Number of pages6
JournalPhysical Chemistry Chemical Physics
Volume20
Issue number42
DOIs
StatePublished - 31 Oct 2018
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018 The Royal Society of Chemistry.

Funding

The authors express their appreciation to the Israel Science Foundation and the National Science Foundation of the People’s Republic of China joint ISF-NSF grant # (2211/15)(51561145006) for funding this research. The research is also made possible, in part, by the generosity of the Harold Perlman Family.

FundersFunder number
ISF-NSF2211/15, 51561145006
National Science Foundation of the People’s Republic of China
Israel Science Foundation

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