Si-rich Al2O3 films grown by RF magnetron sputtering: structural and photoluminescence properties versus annealing treatment
© Korsunska et al.; licensee Springer. 2013
Received: 6 October 2012
Accepted: 6 May 2013
Published: 7 June 2013
Silicon-rich Al2O3 films (Si x (Al2O3)1−x) were co-sputtered from two separate silicon and alumina targets onto a long silicon oxide substrate. The effects of different annealing treatments on the structure and light emission of the films versus x were investigated by means of spectroscopic ellipsometry, X-ray diffraction, micro-Raman scattering, and micro-photoluminescence (PL) methods. The formation of amorphous Si clusters upon the deposition process was found for the films with x ≥ 0.38. The annealing treatment of the films at 1,050°C to 1,150°C results in formation of Si nanocrystallites (Si-ncs). It was observed that their size depends on the type of this treatment. The conventional annealing at 1,150°C for 30 min of the samples with x = 0.5 to 0.68 leads to the formation of Si-ncs with the mean size of about 14 nm, whereas rapid thermal annealing of similar samples at 1,050°C for 1 min showed the presence of Si-ncs with sizes of about 5 nm. Two main broad PL bands were observed in the 500- to 900-nm spectral range with peak positions at 575 to 600 nm and 700 to 750 nm accompanied by near-infrared tail. The low-temperature measurement revealed that the intensity of the main PL band did not change with cooling contrary to the behavior expected for quantum confined Si-ncs. Based on the analysis of PL spectrum, it is supposed that the near-infrared PL component originates from the exciton recombination in the Si-ncs. However, the most intense emission in the visible spectral range is due to either defects in matrix or electron states at the Si-nc/matrix interface.
KeywordsSi-rich-Al2O3 Si nanocrystallites Photoluminescence XRD Raman scattering
Silicon nanocrystallites (Si-ncs) attract considerable interest due to a significant transformation of optical and electrical properties in materials that contain them. These changes are caused by the quantum confinement effect [1–3]. Light-emitting Si-ncs embedded in dielectric hosts have potential applications in optoelectronic devices because of their compatibility with the existing manufacturing infrastructure for silicon integrated circuits.
Among different dielectric materials, silicon oxide is the most addressed as a host for Si-ncs [4, 5]. During the last decades, the properties of Si-nc-SiO2 systems have been widely investigated. Bright luminescence in a wide spectral range at room temperature originates from recombination of excitons in Si-ncs; the variation of their sizes allows tuning of the emission wavelength from the blue to the near infrared [3–6]. In addition to the attractive photoluminescence property, these materials can be used for a new generation of solar cells . Furthermore, Si-ncs embedded in dielectric matrices have regained interest as candidates for non-volatile memory applications . However, because of the downscaling of microelectronic devices, silicon oxide met its limit as a gate material due to high leakage current. In this regard, high-k dielectrics such as ZrO2, HfO2, and Al2O3 are considered as promising gate dielectrics due to the lower equivalent oxide thickness. Also, Si-ncs embedded in such high-k host offer a wider application for non-volatile memories due to the higher performance of the corresponding devices [9, 10].
From the photonic application viewpoint, Al2O3 is an interesting host material for optical communication. The relatively higher refractive index of Al2O3 (1.73 at 1.95 eV) in comparison with that of SiO2 (1.46 at 1.95 eV) at similar bandgap energies allows better light confinement, making compact device structures possible. Indeed, alumina-based waveguides that are very important for optical communications have been developed [11, 12]. Alumina co-doped with Si-ncs and Er3+ ions is more promising than similarly co-doped silica due to higher solubility of Er3+ ions in alumina host. However, in spite of promising properties, Si-nc-Al2O3 materials were not well addressed.
Several approaches have been used to form Si-ncs in amorphous and/or crystalline Al2O3. Most known methods are Si ion implantation [13, 14] and electron beam evaporation followed by subsequent high-temperature annealing as well as laser ablation . For these systems, the successful Si-nc formation was already demonstrated. However, in spite of the relative simplicity of magnetron sputtering technique and its wide application for the fabrication of Si-rich SiO2 materials [5, 8], only few groups applied this method for deposition of Si-rich alumina .
The present paper reports the fabrication of Si-rich Al2O3 films with different Si content by magnetron co-sputtering and the effect of post-deposition processing on the structural and luminescent properties of these materials.
The Si-rich Al2O3 films were deposited by radio frequency (RF) magnetron co-sputtering of two separate 2-in. targets (pure Si and Al2O3) on a long quartz substrate at room temperature. The use of long substrate allowed the variation of the composition along film length in a single deposition run. The length and the width of deposited film were 140 and 4 mm, respectively. The distance between the targets and the substrate was fixed at 64 mm. The background vacuum in the chamber was about 1 × 10−5 Pa prior to the deposition with the pure argon plasma. The RF power applied on Si and Al2O3 targets were 40 and 80 W, respectively. Apart from Si-rich Al2O3 films, pure Si and pure Al2O3 were deposited at the same conditions from one target only. The deposition time was 250 min for each deposition run. The as-deposited original films were cut then to smaller (1 cm in length) segments (called hereafter as samples) to simplify the investigation of their properties.
To study the chemical composition of the films, their refractive index and thickness, the spectroscopic ellipsometry measurement was performed by means of a Jobin-Yvon ellipsometer (UVISEL, HORIBA Ltd., Kyoto, Japan), where the incident light was scanned in the range of 1.5 to 4.5 eV under an incident angle of 66.3°. The fitting of the experimental data was performed using DeltaPsi2 software (HORIBA Ltd., Kyoto, Japan)  and allowed to get information about variation of refractive index and thickness along the film length. Additionally, the film thickness was controlled by means of a Dektak 3030 Profilometer (Veeco, Plainview, NY, USA). The thickness obtained by both methods was found to increase gradually from about 660 nm (Al2O3 side) up to about 1,280 nm (Si side).
To form Si-ncs in the alumina host, two post-fabrication treatments were applied. The former was a conventional annealing (CA) in a horizontal furnace at 1,150°C for 30 min in a nitrogen flow. Another one was a rapid thermal annealing (RTA) at 1,050°C for 1 min either in air or nitrogen atmosphere.
To investigate the evolution of the microstructure and the luminescent properties of the films, we applied a Horiba Jobin-Yvon T-64000 Raman spectrometer (HORIBA Ltd., Kyoto, Japan) equipped with confocal microscope and automated piezo-driven XYZ stage. The measurements were performed at the center of each segment. The micro-Raman scattering (μ-RS) and micro-photoluminescence (μ-PL) spectra were detected in 100- to 900-cm−1 and in 500- to 900-nm spectral ranges, respectively. A 488.0-nm line of Ar-Kr ion laser was used as the excitation source. The laser power on the sample surface was always kept below 5 mW to obtain the best signal-to-noise ratio, preventing a laser heating of the investigated sample. The spectral resolution of the spectrometer was less than 0.15 cm−1. X-ray diffraction (XRD) in our study was carried out using Philips X’Pert-MRD diffractometer (PANalytical B.V, Almelo, The Netherlands) with Cu Kα radiation (λ = 0.15418 nm) in a grazing geometry. The structural investigations were performed at 300 K, whereas the PL was measured at 300 and 80 K.
Results and discussion
Spectroscopic ellipsometry analysis
It is known that spectroscopic ellipsometry is a fast, sensitive, and non-destructive method for thin-film characterization [18–20]. It requires no special environments and can be easily integrated into semiconductor processing. The spectral dependencies of ellipsometric angles (Ψ and Δ) are defined from the fundamental equation of ellipsometry , where and are the complex reflection coefficients for parallel and perpendicular polarizations of light, respectively. These dependencies of Ψ and Δ can be fitted with appropriate modeling approaches to extract the film thickness and optical constants (refractive index, n, and extinction coefficient, k) based on the best fit between experimental and simulated spectra [18, 20].
where n∞ is a refractive index at high frequency, f i is an oscillator strength, Γ j is an amortization factor, ω i and ω g are frequencies of free oscillator. Two dependences, Is = I⋅sin2Ψ⋅sinΔ and Ic = I⋅sin2Ψ⋅cosΔ, where and E0 is the amplitude of electric field of incident light, were fitted.
As for Si-rich Al2O3 films grown from both targets, their dispersion curves are found to be between the curves corresponded to pure Al2O3 and amorphous silicon. They demonstrate gradual shift toward the dependence for amorphous Si with Si content increase (Figure 1a). This means that the film can be considered rather as a mixture of Al2O3 and Si (or SiO x with x < 1), then a mixture of Al2O3 with SiO2 similar to the case described for Si-rich HfO2 films . All the films were found to be amorphous as confirmed by Raman scattering and XRD data (see below). Thus, hereafter, we consider our Si-rich Al2O3 film as an effective medium, which macroscopic properties are determined by the relative fractions of Si and Al2O3, i.e., Si x (Al2O3)1−x.
where ε i and ν i are the complex optical dielectric function and volume fraction for the i th component, respectively; ν is the effective dielectric function corresponding to the measured value for the film. The results of this simulation are presented for the n taken at 2.0 eV (Figure 1b). The dots on this curve correspond to the experimental n values obtained by fitting of ellipsometry data (taken also at 2.0 eV). This approach allows rough estimation of the x variation along the film length (Figure 1b). Taking into account Eqs. (2) and (3) and the values of corresponding refractive indexes (Figure 1a), the relative fraction of Si phase was found to vary from x ≈ 0.92 (n = 3.22 ± 0.01; Si-rich side) to x ≈ 0.05 (n = 1.73 ± 0.01; Si-poor side) (Figure 1b). It should be noted that for x > 0.7, our films grown from Si and Al2O3 targets can be considered rather as Al2O3-rich Si films than Si-rich alumina. In this regard, hereafter, the samples with x < 0.7 will be only analyzed.
Raman scattering spectra
Since important information on the structure of amorphous/nanocrystalline silicon can be obtained from its Raman scattering spectra [26, 27], we investigated these spectra for as-deposited and annealed films versus x.
This ωТО shift indicates ‘unrelaxed’ microstructure of a-Si in our samples due to either point defects (caused a ΔΘ distortion) or tensile strain field [26, 27]. Based on Eqs. (4) and (5), the ΔΘ value was found to be ΔΘ ≈ 20° (x = 0.45) and ΔΘ ≈ 18° (x = 0.68) that exceeds significantly the ΔΘ values obtained for ‘relaxed’ a-Si (about ΔΘ = 7° to 11° [26, 27]). This is an evidence of the significant short-range disorder in a-Si phase in our samples, which can result from numerous point defects or small size of a-Si clusters. At the same time, the ΔΘ values obtained from Eq. (6) are much higher: ΔΘ ≈ 70° (x = 0.45) and ΔΘ ≈ 63° (x = 0.68). This can be explained by significant middle-range disorder that can be caused by the contribution of elastic strains [26, 27]. In our case, they are tensile since the ωТО shifts to the lower wavenumbers.
The observation of Raman spectrum of a-Si in the as-deposited films with x ≥ 0.38 is the evidence of a-Si clusters' formation during film deposition. Meanwhile, when x < 0.42, the intensity of the Raman spectra decreases significantly; the ГTO and the ITA/TO values increase, and the ωТО shifts to the lower frequencies. This testifies to disorder enhancement and can be caused by the decrease the sizes and number of a-Si clusters.
After either CA or RTA treatment, a narrow and high-energy peak is observed, indicating the formation of Si nanocrystallites. For both treatments, with the x decrease the peak position (ωТО-Si-nc) slightly shifts toward the higher wavenumbers accompanied by the decrease of its full width at half maximum (ΓTO-Si-nc) (Figure 2b). It is observed in the range of ωТО-Si-nc = 517.3 to 518.6 cm−1 for CA samples and ωТО-Si-nc = 513.6 to 516.0 cm−1 for RTA samples. At the same time, for the samples with the same x values, Raman peak position is essentially controlled by annealing conditions: the increase of temperature and duration results in its high-wavenumber shift (about 5 cm−1) (Figure 2b). Observed variation of the ωТО-Si-nc and ΓTO-Si-nc versus the x (Figure 2b) contradicts to that expected for quantum confinement effect, because with the x decrease, the Si-nc sizes have to reduce, demonstrating the shift of ωТО-Si-nc toward the lower wavenumbers and the increase of the ΓTO-Si-nc.
As one can see from Figure 2b, besides Si-nc-related peak, the features in the ranges from 100 to 180 cm−1 and 420 to 480 cm−1 are present. This means that all annealed samples contain the amorphous silicon phase, which amount increases with the x rise. This can explain the shift of Raman peak position toward lower wavenumbers for higher x values.
It is worth to note that the ωТО-Si-nc for the Si-nc formed in sapphire at 700°C to 1,050°C is observed in the range from 520 to 525 cm−1 and is shifted to the higher-energy side with respect to peak position of intrinsic c-Si. This indicates the Si-nc in sapphire are under the compressive stress . In contrast in our samples, the ωТО-Si-nc is shifted to the lower wavenumbers (below 519 cm−1). This ‘red’ shift can be caused either by the quantum confinement effect or by the tensile strain between the Si-rich Al2O3 film and the quartz substrate. Going further, based on the XRD data obtained for these samples (see below), we can explain this ωТО shift by the strain between the film and the substrate that is in agreement with the μ-RS data obtained for as-deposited samples. It should be noted that most probable explanation of the smaller shift of the ωТО-Si-nc value after CA treatment in comparison with that after RTA one is the relaxation of tensile stress due to longer time and higher temperature of CA treatment.
The presented results show that the ωТО peak position for annealed samples does not allow correct estimation of the variation of Si-nc sizes because of mechanical stress and presence of amorphous Si phase. Thus, an additional study of structural properties of the samples was performed by means of X-ray diffraction method.
XRD diffraction study
The RTA samples showed the same Si-related XRD peaks, but they are broader (Figure 3, inset). There was not significant effect of the atmosphere of the RTA treatment (either air or nitrogen) on XRD patterns. No diffraction peak from crystalline Al2O3 was detected which indicates that the Si-ncs are embedded in an amorphous matrix.
The mean size of the Si-ncs (<dSi>) was calculated using the Scherer formula. It was found that for x = 0.5 to 0.68, they did not depend practically on the x values but were affected by the treatment conditions. The estimation showed that <dSi> ≈ 14 nm for CA samples and <dSi> ≈ 5 nm for RTA samples. However, it does not exclude the existence of the smaller crystallites in the samples.
The comparison of the XRD data (Figure 3) and the μ-RS spectra (Figure 2) obtained for the same annealed samples showed that the ‘red’ shift of the Si-related TO phonon in the μ-RS spectra (to about 517.3 cm−1) is observed for the Si-nc with <dSi> ≈ 14 nm when a quantum confinement effect is negligible. This allows concluding that the tensile stress between the film and the substrate affects significantly the peak position of the TO phonon in Raman scattering spectra (Figure 2).
Light-emitting properties of the samples
PL after conventional annealing treatment
Figure 4 represents the PL spectra of CA samples measured at 300 K. These spectra contain two broad PL bands, whose maxima are observed at 575 to 600 nm and 700 to 750 nm. In the samples with x = 0.5 to 0.68, these PL bands are well separated, whereas for the films with x = 0.38, they are overlapped significantly (Figure 4). For x = 0.18 to 0.32, the PL intensity of the first band (peaked at 575 to 600 nm) appears to exceed essentially the magnitude of the second PL band (centered at 700 to 750 nm), while the contribution of the second band is more pronounced for the samples with x = 0.38 to 0.68. As Figure 4 shows the first band consists of two components with maxima positions at about 560 and about 600 nm. The former one (about 560 nm) is clearly seen in the sample with x = 0.18 and is similar to PL emission from F22+ centers in Al2O3. Furthermore, it presents in other spectra also, testifying to the incorporation of Si inclusions into Al2O3 matrix. At the same time, both components are strongly overlapped in the samples with x = 0.32 to 0.68 (Figure 4).
PL after rapid thermal annealing
The RTA treatment of the samples in nitrogen atmosphere results in the weak PL emission, whereas the RTA treatment in air causes a much brighter visible emission (Figure 4) that is in agreement with the data of Ref. . The broad PL spectrum can be considered as overlapping of several PL bands (similar to the case of CA treatment).
PL spectra of annealed samples versus temperature of measurement
To elucidate the origin of PL emission from the films investigated, the PL spectra were measured also at 80 K. It should be expected that peak position and intensity of PL bands related to defects in oxide matrixes will not change in the intensity and peak position under cooling down to 80 K because of deep-level-related intra-defect transition. In fact, the most oxide defects demonstrate such PL behavior in the 80 to 300 K range. In contrast, the PL band, related to exciton recombination in quantum confinement Si-ncs, has to demonstrate the shift of its peak position to higher-energy side (up to approximately 41 meV) due to Si bandgap increase [30, 31] accompanied by the increase of PL intensity . However, it is worth to note that the appearance of the strains as well as their sign (tensile or compressive) results either in the increase or in the decrease of this PL shift .
As one can see from Figure 6b, in CA samples with the x ≤ 0.32, where PL spectrum is dominated by one band with peak position at 575 to 600 nm, its peak position and intensity do not depend on temperature. Thus, one can conclude that this emission in our Si-rich Al2O3 films originates from the defects. Such a band was observed in Si-rich Al2O3 materials [36, 37] as well as in Si-rich SiO2 samples . In the former case, it was ascribed to F22+ centers in Al2O3, whereas in the latter case to E′ and NBOHC defects in SiO2. Thus, this emission can be ascribed to the defects located near Si-nc/host interface (i.e., in the shell that covered these Si-ncs). This shell can consist of both alumina and silica [13, 16].
The PL spectra of RTA samples are complex, and they have complicated temperature behavior. As one can see from Figure 6a, PL peak position, observed for sample with x = 0.5 at 700 to 750 nm, is independent on temperature, whereas the intensity of short-wavelength wing (500 to 650 nm) does not change with cooling (Figure 6a). At the same time, a broadening of PL band toward longer wavelengths and slight increase of its intensity in maximum are observed. The independence of the intensity of short-wavelength component (500 to 650 nm) is similar to the data obtained for CA samples that allows its ascribing to the radiative recombination of carriers via host defects.
Since PL spectrum of RTA samples contains several overlapped PL components with very weak features, its deconvolution can be hardly performed. Thus, we used the subtraction of the PL spectrum detected at 300 K from that measured at 80 K. It is seen that PL intensity in the 780- to 900-nm spectral range increases with cooling (Figure 6a, curve 3). The most probable reason for this increase is the rise of the contribution of carrier recombination in Si-ncs to the PL spectrum that is in agreement with the data of Ref. [5, 32] (Figure 6a). At the same time, the PL component peaked at 700 to 750 nm can be attributed to the defects located at Si-nc/matrix interface because slight increase of its maximum magnitude is apparently due to overlapping with near-infrared component which intensity increases with cooling (Figure 6a, curve 3).
Based on the PL results, one can conclude that the main contribution to the PL spectra in our samples is given by the carrier recombination through different defects. The high concentration of interface and matrix defect (in particular, the high intensity of PL band at 700 to 750 nm) obviously hinders the observation of exciton recombination.
The effect of annealing treatment on structural and light emission properties of Si phase-rich Al2O3 films with different Si contents was investigated. The formation of amorphous Si clusters upon deposition process was observed for the films with x ≥ 0.38. The annealing results in the formation of Si crystallites whose mean size depends on the type of post-deposition treatment. The conventional annealing of the samples with x = 0.5 to 0.68 causes the formation of Si-ncs with the mean size of about 14 nm, whereas similar samples submitted to rapid thermal annealing show the presence of Si-ncs with sizes of about 5 nm. Two main broad PL bands were observed in the 500- to 900-nm spectral range with peak positions at 575 to 600 nm and 700 to 750 nm as well as near-infrared tail. The low-temperature measurements revealed that the first PL band was unchanged with cooling, while the slight increase of maximum intensity of the second one was obviously due to overlapping with near-infrared band. Such behavior of visible PL bands differs from that expected for quantum confined Si-ncs that allowed ascribing them to interface and/or matrix defects. At the same time, the analysis of PL spectrum shape allows ascribing the near-infrared PL component (780 to 900 nm) to the exciton recombination inside Si-ncs.
This work was supported by the National Academy of Sciences of Ukraine, Ministry of Art and Science of Israel. One of the authors (LK) would like to acknowledge also the French National Research Agency for partial financial support.
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