Room temperature photoluminescence of the freestanding silicon nanocrystals (original) (raw)
Related papers
Applied Physics B, 2009
Blue luminescent colloidal silicon nanocrystals (Si-ncs) were synthesized at room temperature by nanosecond pulsed laser ablation of a single-crystal silicon target in de-ionized water. Irregular Si-nc fragments obtained by laser ablation are stabilized into regularly shaped, spherical, and well-separated aggregates during the aging process in water. Aging in de-ionized water for several weeks improved the photoluminescence (PL) intensity. At least two weeks of aging are necessary for observation of broad blue room temperature PL with a maximum centered at 420 nm. Detailed structural analysis revealed that agglomerates after aging for several months contain Si-ncs with irregular shape smaller than the quantum confinement limit (<5 nm). These blue luminescent Si-ncs dispersed in de-ionized water exhibited a PL decay time of 6 ns, which is much faster than that of Si-ncs prepared in traditional ways (usually on the order of microseconds). The oxidized Si-ncs with quantum confinement effects are responsible for a PL band around 400 nm visible to the naked eye at room temperature.
Luminescent silicon nanostructures synthesized by laser ablation
physica status solidi (a), 2007
This paper describes the properties of silicon nanostructures synthesized by laser ablation. This is an extremely flexible technique allowing the fabrication of different kinds of nanostructures including porous films and Si nanocrystals embedded in Si oxide. Quantum confinement effects in nanostructures of indirect bandgap semiconductors have attracted great interest due to their new optical properties. This improvement of the efficiency of silicon in emitting light is a first step towards the integration of silicon in optoelectronics. Many groups are working on developing fabrication methods of Si nanocrystals and on the optimization of their luminescence properties. In particular, we describe in detail the mechanisms that govern nucleation and growth of these photoluminescent nanostructures.
Optics Express, 2009
Even with intensive research, air-stable blue light emission from silicon nanocrystals (Si-ncs) at room temperature still remains a challenge. We show that stable and blue-luminescent Si-ncs can be produced by lasergenerated plasma (nanosecond-pulsed excimer laser) confined in water. These Si-ncs exhibit quantum confinement effect due to their size and are produced with an environmentally compatible process. The effect of aging for several weeks in water and air on blue Si-ncs emission properties is compared. The oxide shell around the nanocrystalline core formed during laser processing in water offers the required conditions for the confinement of excitons that allow for stable (in either air or water) blue photoluminescence at room temperature.
Journal of Applied Physics, 2017
Silicon nanoparticles (SiNPs) are attracting attention for applications in various fields, from energy storage to bio-imaging. One of their main advantages is good photoluminescence (PL) properties combined with the relatively high bio-compatibility. Here, we fabricated SiNPs by the laser ablation of silicon single crystal in de-ionized water, employing simultaneously the picosecond pulse laser (150 ps, 1064 nm, 7 mJ/pulse) and a continuous wave (CW) laser (532 nm, 270 mW). TEM analysis (bright field TEM, HRTEM, HAADF, EDS) clearly shows that the introduction of the CW laser significantly increases the crystallinity of the produced nanoparticles, which may be crucial for many optical and electronic applications. The obtained SiNPs exhibit good blue photoluminescence properties, and the introduction of the CW laser into the fabrication process leads to the considerable increases in the photoluminescence. Additionally, we conducted a detailed analysis on the aging-time dependence and the excitation wavelength-dependent PL. The results indicate that the blue photoluminescence may be ascribed to quantum confinement effect, interface related states, and defect in the O-containing layer (shell) of the nanoparticles. We demonstrate that the relative share of these mechanisms in overall PL is significantly affected by the introduction of the CW laser to the pulse laser ablation and it may improve the applicability of the Si nanoparticles produced to a wide variety of fields. Published by AIP Publishing.
MRS Proceedings, 2008
The surface states of silicon nanocrystals (Si-ncs) considerably affect quantum confinement effects and may determinate final nanocrystals properties. Colloidally dispersed Sincs offer larger freedom for surface modification compared to common plasma enhanced chemical vapor deposition or epitaxial synthesis in a solid matrix. The Si-ncs fabrication and elaboration in water by pulsed laser processing is an attractive alternative for controlling and engineering of nanocrystal surface by environmentally compatible way. We report on the possibility of direct silicon surface ablation and Si-ncs fabrication by nanosecond pulsed laser fragmentation of electrochemically etched Si micrograins and by laser ablation of crystalline silicon target immersed in de-ionized water. Two nanosecond pulsed lasers (Nd:YAG, and excimer KrF) are successfully employed to assure fragmentation and ablation in order to produce silicon nanoparticles . Contrary to the fragmentation process, which is more efficient under Nd:YAG irradiation, the laser ablation by both lasers led to the fabrication of fine and room temperature photoluminescent Si-ncs. The processing that has natural compatibility with the environment and advanced state of fabrication technologies may imply new possibilities and applications.
The Journal of Physical Chemistry C, 2012
Blue luminescent colloidal silicon nanocrystals (Si-NCs) were produced in a two-stage process. In the first step, synthesis of Si-NCs was achieved by femtosecond pulsed laser ablation of a silicon wafer, which was immersed in deionized water. The size and the structural and the chemical characteristics of colloidal Si-NCs were investigated by TEM and EDAX analyses, and it is found out that the Si-NCs are in spherical shape and the particle diameters are in the range of 5−100 nm. In the second step, ultrasonic waves and filtering chemical-free post-treatment of colloidal Si-NCs solution was performed to reduce the particle size. High-resolution TEM (HRTEM) studies on post-treated colloidal solution clearly show that small (1−5.5 nm in diameter) Si-NCs were successfully produced. Raman spectroscopy results clearly confirms the generation of Si nanoparticles in the crystalline nature, and the Raman scattering study of post-treated Si-NCs confirms the reduction of the particle size. The UV−vis absorption and photoluminescence (PL) spectroscopy studies elucidate the quantum confinement effect of Si-NCs on the optical properties. The colloidal Si-NCs and post-treated Si-NCs solutions present strong absorption edge shifts toward UV region. Broadband PL emission behavior is observed for the initial colloidal Si-NCs, and the PL spectrum of post-treated Si-NCs presents a blue-shifted broadband PL emission behavior due to the particle size reduction effect.
Optical Materials Express, 2012
In this work, stable blue-green luminescent colloidal silicon nanocrystals (SiNCs) are fabricated by nanosecond pulsed laser ablation of a silicon target in dimethyl sulfoxide (DMSO). Transmission electron microscopy and X-ray diffraction analysis have shown the formation of spherical silicon nanocrystals in the colloid with size range of 2-5 nm. Our results show that the DMSO stabilizes the silicon nanocrystals via oxide formations on the nanocrytals surfaces by a simple route of laser ablation and a schematic representation of the process is suggested. The colloid exhibits strong blue luminescent emissions in the spectral range of 455-465 nm when excited at wavelengths near the direct band gap of the silicon nanocrystal. The luminescent emission band shifts to longer wavelengths (green light) if the excitation wavelength increases toward the indirect band gap of the SiNCs. The oxidized SiNCs with quantum confinement effects are shown to be responsible for visible photoluminescence of the colloid. The observed blue-green emission of the colloid makes it a good candidate for display, solid-state lighting and biological luminescent based devices.