25.01.2008
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 25.01.2008   Карта сайта     Language По-русски По-английски
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25.01.2008

Nature 451, 445-448 (24 January 2008) | doi:10.1038/nature06442; Received 3 July 2007; Accepted 25 October 2007



Emergent reduction of electronic state dimensionality in dense ordered Li-Be alloys


Ji Feng1,4, Richard G. Hennig2, N. W. Ashcroft3 & Roald Hoffmann1




  1. Department of Chemistry and Chemical Biology, Cornell University, Baker Laboratory, Ithaca, New York 14853-1301, USA
  2. Department of Materials Science and Engineering, Cornell University, Bard Hall, Ithaca, New York 14853-1501, USA
  3. Laboratory of Atomic and Solid State Physics and Cornell Center for Materials Research, Cornell University, Clark Hall, Ithaca, New York 14853-2501, USA
  4. Present address: Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.


Correspondence to: N. W. Ashcroft3Roald Hoffmann1 Correspondence and requests for materials should be addressed to N.W.A. (Email: nwa@ccmr.cornell.edu) and R.H. (Email: rh34@cornell.edu).




High pressure is known to influence electronic structure and crystal packing, and can in some cases even induce compound formation between elements that do not bond under ambient conditions1, 2, 3. Here we present a computational study showing that high pressure fundamentally alters the reactivity of the light elements lithium (Li) and beryllium (Be), which are the first of the metals in the condensed state and immiscible under normal conditions4, 5. We identify four stoichiometric LixBe1-x compounds that are stable over a range of pressures, and find that the electronic density of states of one of them displays a remarkable step-like feature near the bottom of the valence band and then remains almost constant with increasing energy. These characteristics are typical of a quasi-two-dimensional electronic structure, the emergence of which in a three-dimensional environment is rather unexpected. We attribute this observation to large size differences between the ionic cores of Li and Be: as the density increases, the Li cores start to overlap and thereby expel valence electrons into quasi-two-dimensional layers characterized by delocalized free-particle-like states in the vicinity of Be ions.



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