Published December 1996 | Version v1
Journal article

Site dependence of large oxygen isotope effect in Y0.7Pr0.3Ba2Cu3O6.97

  • 1. Morris Research, Inc., 44 Marguerita Road, Kensington, California 94707 (United States)
  • 2. Center for Advanced Materials, Lawrence Berkeley Laboratory, Berkeley, California 94720 (United States)

Description

We report site-selective oxygen isotope effects on Tc and penetration depth in Y0.7Pr0.3Ba2Cu3O6.97 and in YBa2Cu3O7-δ. In Pr-substituted (underdoped) samples with 18O in only the CuO2 plane-sites, the Tc shift was -1.46 K vs -1.7 K for 18O at all sites; the αO values are 0.2 and 0.24. The corresponding Tc shifts in pure YBa2Cu3O7-δ were -0.24 K and -0.3 K. The shift is dominated by CuO2 planar oxygen mass in both compounds, and not by the apical sites. Thus, apical site isotope induced charge transfer to CuO2 planes does not seem a viable explanation for the isotope effects in YBCO. Our results indicate that the oxygen related phonons in the CuO2 planes play a significant role in the pairing mechanism. copyright 1996 The American Physical Society

Additional details

Publishing Information

Journal Title
Physical Review. B, Condensed Matter
Journal Volume
54
Journal Issue
21
Journal Page Range
p. 14982-14985.
ISSN
0163-1829
CODEN
PRBMDO