- Nano Express
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Visible and infrared emission from Si/Ge nanowires synthesized by metal-assisted wet etching
© Irrera et al.; licensee Springer. 2014
Received: 4 December 2013
Accepted: 30 January 2014
Published: 12 February 2014
Multi-quantum well Si/Ge nanowires (NWs) were realized by combining molecular beam epitaxy deposition and metal-assisted wet etching, which is a low-cost technique for the synthesis of extremely dense (about 1011 cm−2) arrays of NWs with a high and controllable aspect ratio. In particular, we prepared ultrathin Si/Ge NWs having a mean diameter of about 8 nm and lengths spanning from 1.0 to 2.7 μm. NW diameter is compatible with the occurrence of quantum confinement effects and, accordingly, we observed light emission assignable to the presence of Si and Ge nanostructures. We performed a detailed study of the photoluminescence properties of the NWs, with particular attention to the excitation and de-excitation properties as a function of the temperature and of the excitation photon flux, evaluating the excitation cross section and investigating the presence of non-radiative phenomena.
61.46.Km; 78.55.-m; 78.67.Lt
Semiconductor nanowires (NWs) represent a very promising material to become the building blocks for future electronic  and photonic [2, 3] devices, photovoltaic cells [3, 4], and sensors . Further unexpected applications can be foreseen by fully exploiting the enhanced potentialities of NWs composed by more than a single semiconductor; within this context, the presence of Si/Ge multi-quantum wells (MQWs) inside a NW could be particularly intriguing because it allows putting together two different confined semiconductors, which absorb and emit photons at different wavelengths. In spite their enormous potentialities, the current research on Si/Ge NWs is still in a quite preliminary stage, mainly as far as their light emission properties are concerned , due to the difficulties involved with their synthesis. In fact, ‘bottom-up’ approaches based on the vapor–liquid-solid growth (VLS) mechanism , due to the presence of the Gibbs-Thomson effect, do not allow obtaining the NW diameter values (lower than 10 nm) which are necessary to observe light emission. Furthermore, the metal catalyst (generally Au) used in VLS-based approaches is usually incorporated inside the growing NWs, acting as a deep non-radiative recombination center, negatively altering both electrical and optical properties .
Metal-assisted wet etching processes were recently proposed as a very promising alternative method for the synthesis of Si NWs having a size compatible with the occurrence of quantum confinement effects [9, 10]. In these processes, the role of metal is to catalyze Si oxidation induced by H2O2; afterwards, SiO2, selectively formed where metal and Si are in contact, is etched by HF. Metal catalysts are usually added to the etching solution as a salt (typically AgNO3) ; however, this approach leads to the formation of dendrites, whose subsequent removal can damage the NWs . Note also that NWs with sizes compatible with quantum confinement effects were never obtained by etching processes assisted by metal salts . Recently, we proposed a modified metal-assisted wet etching process, in which the salt was replaced by a thin metal film [2, 12, 13]. This process was demonstrated to be a fast and low-cost technique to fabricate Si NWs since it does not require any kind of expensive and time-consuming lithographic techniques. It also allows the control of several structural parameters like aspect ratio, diameter, density, orientation, and doping type and level; in particular, a unique feature of this process is the possibility to obtain NWs with an extremely small diameter, such as to exhibit a strong light emission at room temperature due to quantum confinement effects [2, 12]. Moreover, since metal-assisted etching is accomplished at room temperature, metal is not incorporated inside the NWs, but it remains trapped at the bottom of the etched regions and can be easily removed by an appropriate etching solution. Metal-assisted wet etching was already used for the synthesis of Si/Ge NWs; the proposed procedure involves the pre-patterning of the substrate by anodic aluminium oxide masks, but no light emission was reported .
In this paper, we demonstrate that it is possible to synthesize light-emitting Si/Ge NWs by metal-assisted wet etching of Si/Ge MQW grown by molecular beam epitaxy (MBE) on a Si substrate. We report a detailed study on the structural and optical properties of this system which, remarkably, exhibits both visible (due to Si) and infrared (IR; due to Ge) light emissions.
NW structural characterization was performed by scanning electron microscopy (SEM) and Raman spectroscopy. SEM analyses were performed using a field emission Zeiss Supra 25 microscope (Oberkochen, Germany). Micro-Raman spectra were acquired using a HR800 spectrometer (Horiba-Jobin Yvon, Kyoto, Japan), exciting the system with the 364-nm line of an Ar+ laser, that allows to avoid the spectral contribution of the substrate due to its low penetration depth in Si (about 12 nm). The exciting beam has a power of 20 μW to prevent heating effects and it was focused on the sample with about 1 μm2 spot area through a fluorinated × 60 (NA = 0.9) Olympus microscope objective (Tokyo, Japan).
Photoluminescence (PL) measurements were performed by pumping with the 488-nm line of an Ar+ laser. Pump power was varied from 1 to 200 mW, corresponding to a photon flux φ ranging from 3.1 × 1019 to 6.2 × 1021 cm−2 · s−1, and the laser beam was chopped through an acousto-optic modulator at a frequency of 55 Hz. The PL signal was analyzed by a single-grating monochromator and detected by a photomultiplier tube in the visible and by a liquid-nitrogen-cooled Ge detector or an IR-extended photomultiplier tube in the IR. Spectra were recorded with a lock-in amplifier using the acousto-optic modulator frequency as a reference. Time-resolved measurements were made by pumping the system at a steady state, then switching off the laser beam, and detecting how the PL signal at a fixed wavelength decreases as a function of time. The overall time resolution of the system is 200 ns. Low-temperature measurements were performed by using a closed cycle He cryostat with the samples kept in vacuum at a pressure of 10−5 Torr.
Results and discussion
Relevant variations of the PL spectrum are found by decreasing the temperature down to 11 K. Indeed, the intensity of the Si-related signal strongly decreases by decreasing temperature, as previously reported in the case of pure Si NWs . On the other hand, a PL signal appears in the IR region at about 1,240 nm (red squares), as shown in Figure 5b. The peak position is in agreement with literature data concerning light emission from Ge nanostructures [19–21]. It is noteworthy that the emission is enhanced by about a factor of 5 with respect to that one coming from the unetched MQW, shown in the same figure as blue squares, which suggests that stronger quantum confinement effects are operating in the NWs (where Ge regions can be considered as nanodots) with respect to the MQW. To this end, we also underline that NWs cover only about the 50% of the sample surface, so that the actual enhancement factor of the PL intensity for Si/Ge NWs accounts for at least an order of magnitude. Although ultrathin Si/Ge NWs were already successfully synthesized [6, 14], to our knowledge, the above-reported data constitute the first evidence of simultaneous light emission from both Si and Ge nanostructures in Si/Ge NWs.
We also measured the time-decay curves of the Ge-related PL signal at 1,220 nm as a function of the temperature, as shown in Figure 6b. Decays become faster by increasing the temperature and cannot be fitted by a single exponential function, so that lifetime (τ) values were evaluated by taking the time at which the PL signal becomes 1/e of its initial value. The observed decreasing τ values from 7.0 μs at 11 K to 0.6 μs at 80 K provide a clear evidence that non-radiative phenomena occur and quench the luminescence. This behaviour is a clear indication of the fact that fast non-radiative phenomena, such as Auger processes or thermally activated quenching processes , influence the de-excitation of Si/Ge NWs. The efficiency of such processes increases by increasing the temperature; indeed, they are able to completely quench the IR PL signal at room temperature.
where N is the total amount of excitable emitting centers, N* is the excited emitting center population, σ is the excitation cross section, φ is the photon flux impinging on the sample, and τ is the lifetime of the excited state, taking into account both radiative and non-radiative processes.
where is the saturation value of IPL. From a fit to the data of Figure 7a by using Equation 2 (shown as a red line), we obtain a στ value of 5.3 × 10−22 cm2 · s−1. Since the lifetime value is 0.5 μs, the measured excitation cross section results to be 1.1 × 10−15 cm2. We remark that, in the presence of Auger processes, the measured lifetime is a function of the excitation density, so that the use of a constant lifetime in Equation 1 represents an approximation. Accordingly, the analysis shown in Figure 7a essentially leads to an estimate of the order of magnitude of the excitation cross section, which however results in good agreement with literature data on Ge nanostructures .
We have demonstrated that a metal-assisted wet etching process can be effectively used to etch Si/Ge MQW and to produce ultrathin Si/Ge NWs which exhibit room temperature PL in the visible range, due to quantum-confined Si nanostructures, and low-temperature PL in the IR range, due to the nanometric Ge layers.
The IR PL emission from the Ge nanostructures is strongly influenced by the occurrence of non-radiative Auger processes, which determines a strong temperature quenching of the PL. In spite of this limitation, the capability of the metal-assisted wet etching technique to synthesize wires in which two semiconductors, characterized by different absorption and emission spectra, are put together opens the ways to new and unexpected applications of NWs in photonics and photovoltaics.
The financial support of MIUR through the project ENERGETIC (PON02_00355_3391233) is acknowledged. The authors thank Carmelo Percolla and Salvo Tatì for the expert technical assistance.
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