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Phys. Rev. Lett. 99, 215901 (2007) [4 pages]

Zero Thermal Expansion in a Nanostructured Inorganic-Organic Hybrid Crystal

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Y. Zhang1,*, Z. Islam2, Y. Ren2, P. A. Parilla1, S. P. Ahrenkiel1, P. L. Lee2, A. Mascarenhas1, M. J. McNevin3, I. Naumov4, H.-X. Fu4, X.-Y. Huang5, and J. Li5
1National Renewable Energy Laboratory, 1617 Cole Boulevard, Golden, Colorado 80401, USA
2Advanced Photon Source, Argonne National Laboratory, 9700 S. Cass Avenue, Argonne, Illinois 60439, USA
3Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, USA
4Department of Physics, University of Arkansas, Fayetteville, Arkansas 72701, USA
5Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA

Received 9 May 2007; published 19 November 2007

There are very few materials that exhibit zero thermal expansion (ZTE), and of these even fewer are appropriate for electronic and optoelectronic applications. We find that a multifunctional crystalline hybrid inorganic-organic semiconductor, β-ZnTe(en)0.5 (en denotes ethylenediamine), shows uniaxial ZTE in a very broad temperature range of 4–400 K, and concurrently possesses superior electronic and optical properties. The ZTE behavior is a result of compensation of contraction and expansion of different segments along the inorganic-organic stacking axis. This work suggests an alternative route to designing materials in a nanoscopic scale with ZTE or any desired positive or negative thermal expansion (PTE or NTE), which is supported by preliminary data for ZnTe(pda)0.5 (pda denotes 1,3-propanediamine) with a larger molecule.

© 2007 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevLett.99.215901
DOI:
10.1103/PhysRevLett.99.215901
PACS:
65.40.De, 61.10.−i, 61.46.−w, 63.22.+m

*yong_zhang@nrel.gov