One-Step Femtosecond Laser Ablation Synthesis of Sub-5 Nm Gold Nanoparticles Embedded in Silica

2018 ◽  
Author(s):  
Mallory John ◽  
Katharine Moore Tibbetts

<div> <div> <div> <p>We report the synthesis of silica-gold nanoparticles (silica-Au NPs) using a one-step femtosecond-reactive laser ablation in liquid (fs-RLAL) technique by focusing femtosecond laser pulses onto a silicon wafer immersed in an aqueous KAuCl4 solution. Characterization of the silica-Au NPs revealed two populations of Au NPs: (i) larger, isolated Au NPs with diameter 7.3±2.1 nm, and (ii) smaller Au NPs (3.4±0.8 nm) embedded in an amorphous silica matrix, along with new species of silicon observed from XPS analysis. The catalytic activity of the silica-Au NPs towards the reduction of para-nitrophenol by NaBH4 is significantly higher compared to the control Au NPs synthesized in the absence of a silicon wafer and other Au NPs recently reported in literature. The formation of the two populations of silica-Au NPs is ascribed to reaction dynamics occurring on two distinct timescales. First, the dense electron plasma formed within tens of femtoseconds of the laser pulse initiates reduction of the [AuCl4]– complex, leading to the formation of larger isolated Au NPs. Second, silicon species ejected from the wafer surface hundreds of picoseconds or later after the initial laser pulse reduce the remaining [AuCl4 ]– and encapsulate the growing clusters, forming ultrasmall Au NPs embedded in the silica matrix. The morphologies of the silica-Au NPs generated from fs-RLAL are distinct from those reported in recent RLAL experiments with nanosecond lasers, reflecting distinct mechanisms occurring on the different pulse duration timescales. </p> </div> </div> </div>

Author(s):  
Mallory John ◽  
Katharine Moore Tibbetts

<div> <div> <div> <p>We report the synthesis of silica-gold nanoparticles (silica-Au NPs) using a one-step femtosecond-reactive laser ablation in liquid (fs-RLAL) technique by focusing femtosecond laser pulses onto a silicon wafer immersed in an aqueous KAuCl4 solution. Characterization of the silica-Au NPs revealed two populations of Au NPs: (i) larger, isolated Au NPs with diameter 7.3±2.1 nm, and (ii) smaller Au NPs (3.4±0.8 nm) embedded in an amorphous silica matrix, along with new species of silicon observed from XPS analysis. The catalytic activity of the silica-Au NPs towards the reduction of para-nitrophenol by NaBH4 is significantly higher compared to the control Au NPs synthesized in the absence of a silicon wafer and other Au NPs recently reported in literature. The formation of the two populations of silica-Au NPs is ascribed to reaction dynamics occurring on two distinct timescales. First, the dense electron plasma formed within tens of femtoseconds of the laser pulse initiates reduction of the [AuCl4]– complex, leading to the formation of larger isolated Au NPs. Second, silicon species ejected from the wafer surface hundreds of picoseconds or later after the initial laser pulse reduce the remaining [AuCl4 ]– and encapsulate the growing clusters, forming ultrasmall Au NPs embedded in the silica matrix. The morphologies of the silica-Au NPs generated from fs-RLAL are distinct from those reported in recent RLAL experiments with nanosecond lasers, reflecting distinct mechanisms occurring on the different pulse duration timescales. </p> </div> </div> </div>


Solar Energy ◽  
2018 ◽  
Vol 164 ◽  
pp. 287-291 ◽  
Author(s):  
Jaffar Moideen Yacob Ali ◽  
Vinodh Shanmugam ◽  
Bianca Lim ◽  
Armin G. Aberle ◽  
Thomas Mueller

Micromachines ◽  
2019 ◽  
Vol 10 (6) ◽  
pp. 401 ◽  
Author(s):  
Mizue Mizoshiri ◽  
Keiko Aoyama ◽  
Akira Uetsuki ◽  
Tomoji Ohishi

We have fabricated Cu-based micropatterns in an ambient environment using femtosecond laser direct writing to reduce a glyoxylic acid Cu complex spin-coated onto a glass substrate. To do this, we scanned a train of focused femtosecond laser pulses over the complex film in air, following which the non-irradiated complex was removed by rinsing the substrates with ethanol. A minimum line width of 6.1 µm was obtained at a laser-pulse energy of 0.156 nJ and scanning speeds of 500 and 1000 µm/s. This line width is significantly smaller than that obtained in previous work using a CO2 laser. In addition, the lines are electrically conducting. However, the minimum resistivity of the line pattern was 2.43 × 10−6 Ω·m, which is ~10 times greater than that of the pattern formed using the CO2 laser. An X-ray diffraction analysis suggests that the balance between reduction and re-oxidation of the glyoxylic acid Cu complex determines the nature of the highly reduced Cu patterns in the ambient air.


Author(s):  
Changrui Cheng ◽  
Xianfan Xu

In this work, molecular dynamics (MD) simulations are carried out to study femtosecond laser ablation of a metal, with an emphasis on the understanding of the mechanism of laser ablation. Theoretically, it has been shown that under intense femtosecond laser irradiation, the material can undergo a volumetric phase change process; its temperature can be close to or even above the critical point. MD simulations allow us to determine the transient temperature of the irradiated material as well as the transient thermodynamic state, which explain the mechanisms of femtosecond laser ablation.


1995 ◽  
Vol 397 ◽  
Author(s):  
G. Herbst ◽  
M. Steiner ◽  
G. Marowsky ◽  
E. Matthias

ABSTRACTLaser ablation of silicon and germanium was carried out in moderate vacuum with l00fs to 400fs pulses at 248nm and intensities up to 3x1013 W/cm2. Evidence for non-thermal material removal was found. Imaged multishot ablation patterns display the intensity dependent self-structuring effect, forming well-known columnar structures. It is shown that continued irradiation of these structures eventually results in comparatively clean ablation. An increase of ablation rate with depth was observed. The reason is an intensity enhancement inside the pits by reflective focussing to a level where bond-breaking takes place. Furthermore, it was noticed that ablation contours can be significantly improved by electrically grounding the target.


2007 ◽  
Vol 539-543 ◽  
pp. 1951-1954 ◽  
Author(s):  
Tomokazu Sano ◽  
Kengo Takahashi ◽  
Akio Hirose ◽  
Kojiro F. Kobayashi

Dependence of the femtosecond laser ablation depth on the laser pulse energy was investigated for Zr55Al10Ni5Cu30 bulk metallic glass. Investigation of the femtosecond laser ablation of bulk metallic glasses has not been reported. Femtosecond laser pulses (wavelength of 800 nm, pulse width of 100 fs, pulse energies of 2 – 900 μJ) were focused and irradiated on the polished surface of metals in air. The ablation depth of the metallic glass is deeper than that of its crystallized metal at a pulse energy in the strong ablation region. We suggest that the energy loss at grain boundaries of hot electrons which is accelerated by the laser electric field influence the ablation depth in the strong ablation region.


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