The effects of Au insertion in solid-phase crystallization for amorphous Ge films on SiO2/Si substrates were investigated to achieve oriented crystalline Ge. After high-temperature annealing above 300 °C, Au atoms were highly diffused in the amorphous Ge layer. The resulting crystalline Ge consisted of random grains formed by crystal nucleation in the entire Ge region. However, when annealing temperature was decreased to below 250 °C, Au atoms were localized at their initial position even after a long annealing (20 h). Moreover, formation of preferentially (111)-oriented crystalline Ge was achieved without using the metal-induced layer-exchange crystallization method. These results suggest that crystal nucleation preferentially occurs at the amorphous Ge/Au interface, and subsequently the nucleus growth progresses into the Ge layer.
We report the magnetic dead layer at the interfaces between Fe and Si(111) surfaces. We prepared two ultrathin iron-silicides, c(8×4) prepared at 900 K and p(2×2) at 700 K, and clean reconstructed 7×7 surface for the silicon templates. By using magneto-optical Kerr effect, we found that at room temperature the ferromagnetic order appears at 5.5 ML, 8.2 ML, and 10.9 ML for Fe/c(8×4) silicide, Fe/p(2×2) silicide, and Fe/Si(111)-7×7 surface, respectively. From the thickness dependent magnetization measurements, we decided the magnetic dead layer for Fe/c(8×4) silicide, Fe/p(2×2) silicide, and Fe/Si(111)-7×7 to be 3.0 ML, 5.0 ML, and 7.5 ML, respectively. Our results indicate that the c(8×4) iron silicide surface prevents further silicide formation more effectively than the p(2×2) silicide and Si(111)-7×7 surface.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.