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Huang Hua, Zhu Changfei, Liu Wei. The Prepration of p-Type Transparant Conducting Oxides CuCr1-xCaxO2 and Research about Its Electrical and Optical Property[J]. Chinese Journal of Chemical Physics , 2004, 17(2): 161-164. DOI: 10.1088/1674-0068/17/2/161-164
Citation: Huang Hua, Zhu Changfei, Liu Wei. The Prepration of p-Type Transparant Conducting Oxides CuCr1-xCaxO2 and Research about Its Electrical and Optical Property[J]. Chinese Journal of Chemical Physics , 2004, 17(2): 161-164. DOI: 10.1088/1674-0068/17/2/161-164

The Prepration of p-Type Transparant Conducting Oxides CuCr1-xCaxO2 and Research about Its Electrical and Optical Property

Funds: Project supported by the Chinese Academy of Sciences and the Ministry of Education P. R. C.
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  • Received Date: March 02, 2003
  • Transparant conducting oxides showing the combination of high electrical conductivity and high transparency for visible light have been based on electron doping into a conduction band. For p-type delafossite oxides,the valence band is commonly the oxygen 2p band. Doping to produce holes in this band but the electronic conductivity of such p-type oxides is highly activated and can generally only be measured at temperatures well above room temperature. So it is very desirable to improve conductivity by doping wide-gap delafossites as transparant conducting oxides nowadays. The article reported the prepration and characterization of Ca-doped CuCrO2 monophasic delafossites. It was found that conductivity had a notable improvement after Ca-doped and reached 3. 2×10-2 S/cm for x=0.06 Ca-doped at room temperature and the structures had not been changed. The temperature dependence of electrical conductivity around room temperture was consistent with thermal activation type very well from 200 K to 300 K. The activation energe was 0. 36 eV before doping,but it changed to 0.27 eV when Ca-doped. This phenomenon suggest that in pure non-doped CuCrO2,carrier was the Cu+ d. After Ca-doped,the Cu2+ was formed from the Cu+ by a charge compensating process when the divalent Ca2+ substituted for the trivalent Cr3+ . The Seebeck coefficients being large positive constants implied that all the samples were p-type conducting oxides.
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