Variable-range hopping conduction in epitaxial CrN(001)

X. Y. Zhang, J. S. Chawla, B. M. Howe, and D. Gall
Phys. Rev. B 83, 165205 – Published 25 April 2011

Abstract

Epitaxial CrN(001) layers, grown by dc magnetron sputtering on MgO(001) substrates at growth temperatures Ts = 550–850 °C, exhibit electronic transport that is dominated by variable-range hopping (VRH) at temperatures <120 K. A transition from Efros-Shklovskii to Mott VRH at 30 ± 10 K is well described by a universal scaling relation. The localization length decreases from 1.3 nm at Ts = 550 °C to 0.9 nm for Ts = 600–750 °C, but increases again to 1.9 nm for Ts = 800–850 °C, which is attributed to changes in the density of localized states associated with N vacancies that form due to kinetic barriers for incorporation and enhanced desorption at low and high Ts, respectively. The low-temperature transport data provide lower limits for the CrN effective electron mass of 4.9me, the donor ionization energy of 24 meV, and the critical vacancy concentration for the metal-insulator transition of 8.4 × 1019 cm3. The room temperature conductivity is dominated by Hubbard band states near the mobility edge and decreases monotonically from 137 Ω1cm1 for Ts = 550 °C to 14 Ω1cm1 for Ts = 850 °C due to a decreasing structural disorder, consistent with the measured x-ray coherence length that increases from 7 to 36 nm for Ts = 550 to 850 °C, respectively, and a carrier density that decreases from 4 × 1020 to 0.9 × 1020 cm3, as estimated from optical reflection and Hall effect measurements. The absence of an expected discontinuity in the conductivity at ∼280 K suggests that epitaxial constraints suppress the phase transition to a low-temperature orthorhombic antiferromagnetic phase, such that CrN remains a cubic paramagnetic insulator over the entire measured temperature range of 10–295 K. These results contradict previous experimental studies that report metallic low-temperature conduction for CrN, but support recent computational results suggesting a band gap due to strong electron correlation and a stress-induced phase transition.

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  • Received 21 January 2011

DOI:https://doi.org/10.1103/PhysRevB.83.165205

©2011 American Physical Society

Authors & Affiliations

X. Y. Zhang1, J. S. Chawla1, B. M. Howe2, and D. Gall1

  • 1Department of Materials Science and Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA
  • 2Department of Materials Science and the Frederick Seitz Materials Research Laboratory, University of Illinois, 104 South Goodwin Avenue, Urbana, Illinois 61801, USA

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Vol. 83, Iss. 16 — 15 April 2011

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