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Magnetic Oxide Heterostructures: EuO on Cubic Oxides ... - JuSER

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5.5. Interface engineering III: SiO x passivation of the EuO/Si interface 119<br />

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Figure 5.28.: Consistent peak fit analysis of the SiO x -passivated EuO/Si (001) interface using Si and<br />

Eu core-levels of the HAXPES experiments.<br />

itored by RHEED. Finally, the EuO/Si heterostructures are capped with 5 nm air-protective<br />

Al. In order to investigate the electronic structure at the EuO/Si interface, we conducted<br />

HAXPES studies of the EuO/Si hybrid structures at the undulator beamline P09 at PETRA III<br />

(DESY, Hamburg), 97 and at the KMC-1 dipole beamline at BESSY II (Berlin) with the HIKE<br />

endstation. 98 The Fermi edge of Au foil on the sample serves as calibration for the binding<br />

energy. Tougaard-type backgrounds are used to account for inelastic photoelectron scattering.<br />

Interface-sensitive HAXPES spectra of the EuO/Si heterostructures are depicted in Fig. 5.28a, b.<br />

Stable silicon oxide is observed at chemical shifts of 3.2 and 4.1 eV in the Si 1s spectrum,<br />

which identify Si 3+ (Si 2 O 3 ) and Si 4+ (SiO 2 ), in good agreement with recent PES studies of ultrathin<br />

SiO 2 /Si (001). 139,208 Another component at the EuO/Si interface with a chemical shift<br />

to lower BE is observed in the Si spectra as well as in the Eu3d, 4d, and 4f spectra, which is<br />

identified as a metallic Eu silicide (EuSi y ). Due to the small chemical shift of EuSi y (−0.65 eV<br />

for Si 2p), only the Si spectra and the narrow Eu 4f multiplet allow for a quantitative deconvolution<br />

of the entire silicide fraction silicide components. In case of the complex Eu 3d and<br />

4d multiplets, we can separate only the silicide component of one J final state at the lower<br />

binding energy side. A quantitative thickness determination of the SiO x passivation at the<br />

Si (001) interface and of the resulting silicide reaction layer is accomplished by consistent<br />

least squares peak fitting after Levenberg-Marquard of the HAXPES spectra. The thickness<br />

c of the interfacial passivation (SiO x ) and EuSi y reaction layers are determined from their<br />

relative spectral weight, as derived in equations (3.16) and (3.19) (in Ch. 3.4.4 on p. 51). The<br />

results are compiled in Fig. 5.29. Regarding the chemical reactivity of the EuO/Si interface<br />

we found interfacial silicides to exceed 10 Å thickness for flashed Si (001), however by applying<br />

an ultrathin SiO x interface passivation (d SiOx = 10–13 Å) silicide formation is suppressed

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