XPS determination of the oxygen coefficient k(O) = 2 + x and ionic (U4+, U5+, and U6+) composition of oxides UO(2+)x formed on the surfaces of differently oriented (hkl) planes of thin UO2 films on LSAT (Al10La3O51Sr14Ta7) and YSZ (yttria-stabilized zirconia) substrates was performed. The U 4f and 0 1s core- electron peak intensities as well as the U Sf relative intensity before and after the (129)xe(23)+ and U-238(31+) irradiations were employed. It was found that the presence of uranium dioxide film in air results in formation of oxide UO2+x on the surface with mean oxygen coefficients k(O) in the range 2.07-2.11 on LSAT and 2.17-2.23 on YSZ substrates. These oxygen coefficients depend on the substrate and weakly on the crystallographic orientation. On the basis of the spectral parameters it was established that uranium dioxide films AP2,3 on the LSAT substrates have the smallest ko values, and from the XRD. and EBSD results it follows that these samples have a regular monocrystalline structure. The XRD and EBSD results indicate that samples APS-7 on the YSZ substrates have monocrystalline structure; however, they have the highest k(O) values. The observed difference in the ko values was probably caused by the different nature of the substrates: the YSZ substrates provide 6.4% compressive strain, whereas (001) LSAT substrates result only in 0.03% tensile strain in the UO2 films. Xe-129(23+) irradiation (92 MeV, 4.8 X 10(15) ions/cm(2)) of uranium dioxide films on the LSAT substrates was shown to destroy both long-range ordering and uranium close environment, which results in an increase of uranium oxidation state and regrouping of oxygen ions in uranium dose environment. U-238(31+) (110 MeV, 5 X 10(10), 5 X 10(11), 5 X 10(12) ions/cm(2)) irradiations of uranium dioxide films on the YSZ substrates were shown to form the lattice damage only with partial destruction of the long-range ordering.
机构:
Commiss European Communities, Joint Res Ctr, Inst Transuranium Elements ITU, DE-76125 Karlsruhe, GermanyASCR, Inst Phys, Prague 18221, Czech Republic
Bao, Z.
Havela, L.
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Charles Univ Prague, Fac Math & Phys, CR-12116 Prague, Czech RepublicASCR, Inst Phys, Prague 18221, Czech Republic
机构:
Commiss European Communities, Joint Res Ctr, Inst Transuranium Elements ITU, DE-76125 Karlsruhe, GermanyASCR, Inst Phys, Prague 18221, Czech Republic
Gouder, T.
Caciuffo, R.
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Commiss European Communities, Joint Res Ctr, Inst Transuranium Elements ITU, DE-76125 Karlsruhe, GermanyASCR, Inst Phys, Prague 18221, Czech Republic
机构:
Chalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, SwedenChalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, Sweden
Hansson, N. L.
Tam, P. L.
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Chalmers Univ Technol, Dept Ind & Mat Sci, SE-41296 Gothenburg, SwedenChalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, Sweden
Tam, P. L.
Ekberg, C.
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Chalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, SwedenChalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, Sweden
Ekberg, C.
Spahiu, K.
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Chalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, Sweden
Swedish Nucl Fuel & Waste Management Co, SE-10124 Stockholm, SwedenChalmers Univ Technol, Nucl Chem Ind Mat Recycling, SE-41296 Gothenburg, Sweden