Phys. Rev. B 63, 184507 (2001) [6 pages]O K-edge and Cu L23-edge XANES study on the concentration and distribution of holes in the (Pb2/3Cu1/3)3Sr2(Y, Ca)Cu2O8+z superconductive phase |
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M. Karppinen * and M. Kotiranta
Laboratory of Inorganic and Analytical Chemistry, Helsinki University of Technology, FIN-02015 Espoo, Finland
H. Yamauchi
Materials and Structures Laboratory, Tokyo Institute of Technology, Yokohama 226-8503, Japan
P. Nachimuthu and R. S. Liu
Department of Chemistry, National Taiwan University, Taipei, Taiwan, Republic of China
J. M. Chen
Synchrotron Radiation Research Center (SRRC), Hsinchu, Taiwan, Republic of China
Received 28 August 2000; published 17 April 2001
By means of high-resolution O K-edge and Cu L23-edge x-ray absorption near-edge-structure spectroscopy continuous increase of the CuO2-plane hole concentration with increasing Casubstitution level has been established for the superconductive, oxygen-depleted (z≈0) (Pb2/3Cu1/3)3Sr2(Y1-xCax)Cu2O8+z [(Pb2/3Cu1/3)-3212] phase with a three-layer PbO-Cu-PbO charge-reservoir block. For the O K-edge absorption, a pre-edge peak at ∼528.3 eV is seen, originating from the excitation of the O 1s electron to the O 2p hole state located in the CuO2 plane. With increasing Ca-substitution level, the intensity of this peak continuously increases within the substitution range studied, i.e., 0<~x<~0.5. Consistently, with increasing x, the shoulder on the high-energy side of the main absorption peak at ∼932.0 eV in the Cu L23-edge spectra, i.e., a feature typically assigned to formally trivalent copper, enhances. From the Cu L23-edge spectra it was furthermore confirmed that the charge-reservoir copper remains in the monovalent state, indicating that the holes created through Ca substitution are directed solely into the superconductive CuO2 plane. In terms of increasing the CuO2-plane hole concentration, Ca substitution was found to work more efficiently in (Pb2/3Cu1/3)-3212 as compared to, e.g., the related Bi-2212 phase.
©2001 The American Physical Society
URL: http://link.aps.org/abstract/PRB/v63/e184507
DOI: 10.1103/PhysRevB.63.184507
PACS: 74.62.Dh, 61.10.Ht, 74.72.Jt
* Present address: Materials and Structures Laboratory, Tokyo Institute of Technology, Yokohama 226-8503, Japan.
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