| 1. |
- Barbe, Jeremy, et al.
(författare)
-
Silicon nanocrystals on amorphous silicon carbide alloy thin films : Control of film properties and nanocrystals growth
- 2012
-
Ingår i: Thin Solid Films. - : Elsevier. - 0040-6090 .- 1879-2731. ; 522, s. 136-144
-
Tidskriftsartikel (refereegranskat)abstract
- The present study demonstrates the growth of silicon nanocrystals on amorphous silicon carbide alloy thin films. Amorphous silicon carbide films [a-Si1 − xCx:H (with x < 0.3)] were obtained by plasma enhanced chemical vapor deposition from a mixture of silane and methane diluted in hydrogen. The effect of varying the precursor gas-flow ratio on the film properties was investigated. In particular, a wide optical band gap (2.3 eV) was reached by using a high methane-to-silane flow ratio during the deposition of the a-Si1 − xCx:H layer. The effect of short-time annealing at 700 °C on the composition and properties of the layer was studied by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. It was observed that the silicon-to-carbon ratio in the layer remains unchanged after short-time annealing, but the reorganization of the film due to a large dehydrogenation leads to a higher density of SiC bonds. Moreover, the film remains amorphous after the performed short-time annealing. In a second part, it was shown that a high density (1 × 1012 cm− 2) of silicon nanocrystals can be grown by low pressure chemical vapor deposition on a-Si0.8C0.2 surfaces at 700 °C, from silane diluted in hydrogen. The influence of growth time and silane partial pressure on nanocrystals size and density was studied. It was also found that amorphous silicon carbide surfaces enhance silicon nanocrystal nucleation with respect to SiO2, due to the differences in surface chemical properties.
|
|
| 2. |
- Borges, J., et al.
(författare)
-
Microstructural evolution of Au/TiO2 nanocomposite films : The influence of Au concentration and thermal annealing
- 2015
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 580, s. 77-88
-
Tidskriftsartikel (refereegranskat)abstract
- Nanocomposite thin films consisting of a dielectric matrix, such as titanium oxide (TiO2), with embedded gold (Au) nanoparticles were prepared and will be analysed and discussed in detail in the present work. The evolution of morphological and structural features was studied for a wide range of Au concentrations and for annealing treatments in air, for temperatures ranging from 200 to 800 degrees C. Major findings revealed that for low Au atomic concentrations (at.%), there are only traces of clustering, and just for relatively high annealing temperatures, T >= 500 degrees C. Furthermore, the number of Au nanoparticles is extremely low, even for the highest annealing temperature, T = 800 degrees C. It is noteworthy that the TiO2 matrix also crystallizes in the anatase phase for annealing temperatures above 300 degrees C. For intermediate Au contents (5 at.% <= C-Au <= 15 at.%), the formation of gold nanoclusters was much more evident, beginning at lower annealing temperatures (T >= 200 degrees C) with sizes ranging from 2 to 25 nm as the temperature increased. A change in the matrix crystallization from anatase to rutile was also observed in this intermediate range of compositions. For the highest Au concentrations (>20 at.%), the films tended to form relatively larger clusters, with sizes above 20 nm (for T >= 400 degrees C). It is demonstrated that the structural and morphological characteristics of the films are strongly affected by the annealing temperature, as well as by the particular amounts, size and distribution of the Au nanoparticles dispersed in the TiO2 matrix.
|
|
| 3. |
- Borges, J., et al.
(författare)
-
Thin films composed of gold nanoparticles dispersed in a dielectric matrix : The influence of the host matrix on the optical and mechanical responses
- 2015
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 596, s. 8-17
-
Tidskriftsartikel (refereegranskat)abstract
- Gold nanoparticles were dispersed in two different dielectric matrices, TiO2 and Al2O3, using magnetron sputtering and a post-deposition annealing treatment. The main goal of the present work was to study how the two different host dielectric matrices, and the resulting microstructure evolution (including both the nanoparticles and the host matrix itself) promoted by thermal annealing, influenced the physical properties of the films. In particular, the structure and morphology of the nanocomposites were correlated with the optical response of the thin films, namely their localized surface plasmon resonance (LSPR) characteristics. Furthermore, and in order to scan the future application of the two thin film system in different types of sensors (namely biological ones), their functional behaviour (hardness and Young's modulus change) was also evaluated. Despite the similar Au concentrations in both matrices (similar to 11 at.%), very different microstructural features were observed, which were found to depend strongly on the annealing temperature. The main structural differences included: (i) the early crystallization of the TiO2 host matrix, while the Al2O3 one remained amorphous up to 800 degrees C; (ii) different grain size evolution behaviours with the annealing temperature, namely an almost linear increase for the Au:TiO2 system (from 3 to 11 nm), and the approximately constant values observed in the Au:Al2O3 system (4-5 nm). The results from the nanoparticle size distributions were also found to be quite sensitive to the surrounding matrix, suggesting different mechanisms for the nanoparticle growth (particle migration and coalescence dominating in TiO2 and Ostwald ripening in Al2O3). These different clustering behaviours induced different transmittance-LSPR responses and a good mechanical stability, which opens the possibility for future use of these nanocomposite thin film systems in some envisaged applications (e.g. LSPR-biosensors).
|
|
| 4. |
- Donzel-Gargand, Olivier, 1986-, et al.
(författare)
-
Surface defect passivation by a thin metallic barrier for Cu(InxGa1-x)Se2 co-evaporation on Cr-steel substrates
- 2016
-
Ingår i: Thin Solid Films. - : Elsevier. - 0040-6090 .- 1879-2731. ; 619, s. 220-226
-
Tidskriftsartikel (refereegranskat)abstract
- The use of Cr-steel substrates for the fabrication of Cu(In,Ga)Se2 (CIGS) solar cells is highly desirable and is a topic of considerable research interest. However, solar cells on non-treated steel substrates often exhibit decreased performance compared to their homologues on soda lime glass substrates. This is partly attributed to out-diffusion of steel components (Fe, Cr, Mn, etc.) into the solar cell. To avoid this contamination, thin film barriers can be added on top of the steel surface, but they do not always prevent the diffusion completely. In this paper we study the potential of using Cr and Ti as thin barrier layers. We find that local surface defects on the steel, several micrometers in height, lead to cracks in the back contact as well as in the barrier layers. Advanced transmission electron microscopy (TEM) techniques reveal that elemental diffusion and chemical reactions occur at these openings during heat treatments in Se atmosphere. TEM-energy dispersive X-ray spectroscopy (TEM-EDX) analysis in combination with calculation of the solid state diffusion coefficient demonstrate that a Cr-barrier sacrificially protects the Cr-steel substrate, blocking most of the Fe out-diffusion, whereas a Ti-barrier is less efficient.
|
|
| 5. |
- Droulias, Sotirios A., et al.
(författare)
-
Crystal perfection by strain engineering : The case of Fe/V (001)
- 2017
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 636, s. 608-614
-
Tidskriftsartikel (refereegranskat)abstract
- We study the effect of bilayer thickness at fixed volume fraction on the structural quality of Fe/V (001)superlattices. We find that such artificial metallic superlattices can be manufactured with excellent crystalquality and layering up to at least 50 Å in repeat distance (K = LFe +LV). For an intended fixed ratio of theconstituents: LFe/LV= 1/7, out-of-plane coherence lengths comparable to the thicknesses of the sampleswere obtained. We evaluate the strain in- and out-of-plane of both layers as a function of the bilayer thicknessand comment on the growth using the framework of linear elasticity theory. We interpret the stabilityof the superlattice against crystal degradation due to the alternating compressive and tensile strain, yieldingclose to ideal lattice matching to the substrate.
|
|
| 6. |
- Frisk, Andreas, 1983-, et al.
(författare)
-
Composition, structure and magnetic properties of ultra-thin Fe/Ni multilayers sputter deposited on epitaxial Cu/Si(001)
- 2018
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 646, s. 117-125
-
Tidskriftsartikel (refereegranskat)abstract
- Sputter deposited symmetric multilayers of (n Fe)/(n Ni), with individual thicknesses from n = 4 to n = 48 monolayers (ML), were deposited on epitaxial Cu/Si(001), and their microstructural evolution and magnetic properties versus n have been studied. Elemental layering can be seen with transmission electron microscopy down to n = 4 ML layer thickness, although an intermixed region characterized by a finite interface width is found to be present. This width is composed of the interface roughness as well as the interdiffusion between layers, but the relative contributions from these two sources could not be concluded by the techniques used. The measured elemental layering and X-ray reflectivity (XRR) give an upper limit to the interface width which must be smaller than the thinnest layers, 4 ML. Electron energy loss spectroscopy (EELS), depth profiling X-ray photoelectron spectroscopy (XPS) and also XRR reveal that Fe has a higher tendency to mix with Ni than vice versa. XPS does not have the resolution to measure this thin elemental layering: composition variations for n = 8 ML which are clearly seen by EELS are barely resolved by XPS. The structure was determined by X-ray diffraction, and an epitaxial fcc (001) structure is found to be maintained throughout the multilayers up to n less than or similar to 8 ML. For larger n values, relaxation starts by Fe-fcc(001) layers changing into Fe-bcc(110), which is then followed by Ni-fcc(001) changing from (001) to (111) orientation along the growth direction. A decreased total measured magnetic moment for the fully epitaxial multilayers can be explained by the fcc Fe layers being partly anti-ferromagnetic, whereas the relaxed multilayers exhibit the expected magnetic properties of (bcc Fe) +(fcc Ni).
|
|
| 7. |
- Korelis, Panagiotis T., et al.
(författare)
-
Highly amorphous Fe90Zr10 thin films, and the influence of crystallites on the magnetism
- 2010
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 519:1, s. 404-409
-
Tidskriftsartikel (refereegranskat)abstract
- A method for depositing highly amorphous, iron-rich Fe100-xZrx thin films on to room temperature substrates is presented. The method involves co-depositing Fe and Zr on to an amorphous AlZr layer. Experimental proof that the structures are completely amorphous is given by transmission electron microscopy and polarized neutron reflectometry. The reflectometry measurements also give an indication of the impact that Fe crystallite impurities have on the magnetic structure and properties of amorphous FeZr. The results are consistent with previous investigations on bulk samples, which showed that crystalline impurities make the magnetic structure more non-collinear.
|
|
| 8. |
|
|
