Time resolved optical emission spectroscopy of cross-beam pulsed laser ablation on graphite targets

2007 ◽  
Vol 367 (4-5) ◽  
pp. 351-355 ◽  
Author(s):  
R. Sanginés ◽  
C. Sánchez Aké ◽  
H. Sobral ◽  
M. Villagrán-Muniz
Keyword(s):  
Laser Ablation ◽  
Emission Spectroscopy ◽  
Optical Emission Spectroscopy ◽  
Pulsed Laser ◽  
Optical Emission ◽  
Pulsed Laser Ablation ◽  
Time Resolved

Pulsed laser ablation-deposition of La0.5Sr0.5CoO3 for use as electrodes in nonvolatile ferroelectric memories

1996 ◽  
Vol 11 (6) ◽  
pp. 1514-1519 ◽  
Author(s):  
R. Dat ◽  
O. Auciello ◽  
D. J. Lichtenwalner ◽  
A. I. Kingon
Keyword(s):  
Laser Ablation ◽  
Emission Spectroscopy ◽  
Smooth Surface ◽  
Optical Emission Spectroscopy ◽  
Pulsed Laser ◽  
Optical Emission ◽  
Pulsed Laser Ablation ◽  
Deposition Parameters ◽  
Ferroelectric Memories ◽  
Oxygen Interaction

La0.5Sr0.5CoO3 (LSCO) thin films have been deposited on (100) MgO substrates using pulsed laser ablation-deposition (PLAD). The crystallographic orientation of LSCO was found to be dependent on the surface treatment of (100) MgO prior to deposition. PLAD deposition parameters were optimized to yield LSCO films with an RMS surface roughness of 40–50 Å. A smooth surface morphology was reproduced as long as the oxygen content of the LSCO target was preserved. Otherwise, “splashing” occurred which resulted in the transfer of condensed particles from molten spherical globules of LSCO from the target to the substrate. Splashing was subsequently eliminated and smooth surface quality was restored after annealing the LSCO target at 550 °C in oxygen for 3 h. Optical emission spectroscopy (OES) of the LSCO's plume identified excited atomic cobalt neutrals, excited singly ionized strontium and lanthanum, and excited molecular LaO species. Oxygen interaction with the plume produced no new species. Furthermore, the OES data suggest that the observed LaO molecules were not created by the chemical reaction between La and O2 during ablation, but were ejected directly from the target during the PLAD process.

scholarly journals Imaging spectroscopy of Ag plasmas produced by infrared nanosecond laser ablation

2019 ◽  
Vol 34 (3) ◽  
pp. 489-497 ◽  
Author(s):  
J. J. Camacho ◽  
M. Oujja ◽  
M. Sanz ◽  
A. Martínez-Hernández ◽  
I. Lopez-Quintas ◽  
...  
Keyword(s):  
Laser Ablation ◽  
Emission Spectroscopy ◽  
Optical Emission Spectroscopy ◽  
Imaging Spectroscopy ◽  
Pulsed Laser ◽  
Optical Emission ◽  
Pulsed Laser Ablation ◽  
Nanosecond Laser ◽  
Nanosecond Laser Ablation

Spatially and temporally resolved optical emission spectroscopy has been used to study plasmas formed by 1064 nm pulsed laser ablation of silver targets in a vacuum.

scholarly journals Dynamics of Transient Plasmas Generated by ns Laser Ablation of Memory Shape Alloys

2020 ◽  
Author(s):  
Stefan Andrei Irimiciuc ◽  
Norina Forna ◽  
Andrei Agop ◽  
Maricel Agop ◽  
Stefan Toma ◽  
...  
Keyword(s):  
Laser Ablation ◽  
Pulsed Laser Deposition ◽  
Emission Spectroscopy ◽  
Pulsed Laser ◽  
Optical Emission ◽  
Laser Deposition ◽  
Global Dynamics ◽  
Time Resolved ◽  
Laser Ablation Process ◽  
Key Techniques

Understanding the underline fundamental mechanism behind experimental and industrial technologies embodies one of the foundations of the advances and tailoring new materials. With the pulsed laser deposition being one of the key techniques for obtaining complex biocompatible materials with controllable stoichiometry, there is need for experimental and theoretical advancements towards understanding the dynamics of multi component plasmas. Here we investigate the laser ablation process on Cu-Mn-Al and Fe-Mn-Si by means of space-and time-resolved optical emission spectroscopy and fast camera imaging. In a fractal paradigm the space–time homographic transformations were correlated with the global dynamics of the ablation plasmas.

Optical Detection of Slow Excited Neutrals in Plasma-Assisted Excimer Laser Ablation

1995 ◽  
Vol 397 ◽  
Author(s):  
P. Mukherjee ◽  
P. Sakthivel ◽  
S. Witanachchi
Keyword(s):  
Laser Ablation ◽  
Excimer Laser ◽  
Emission Spectroscopy ◽  
Optical Emission Spectroscopy ◽  
Temporal Dynamics ◽  
Optical Emission ◽  
Ring Electrode ◽  
Time Resolved ◽  
Excimer Laser Ablation ◽  
Slow Moving

ABSTRACTThe observation of a slow optically excited component in the excimer laser-ablated YBCO plume due to the presence of a biased ring electrode is reported. The temporal dynamics of the plume were investigated by using time-of-flight (TOF) optical emission spectroscopy (OES). Time-resolved emission signals reveal excitation and resultant fluorescence from slow-moving plume species in the presence of the discharge.

scholarly journals Time-Resolved Quadrupole Mass Spectrometric Studies on Pulsed Laser Ablation of TiO2

1999 ◽  
Vol 18 (3) ◽  
pp. 99-109 ◽  
Author(s):  
Yongxin Tang ◽  
Zhenhui Han ◽  
Qizong Qin
Keyword(s):  
Laser Ablation ◽  
Continuous Wave ◽  
Center Of Mass ◽  
Pulsed Laser ◽  
Pulsed Laser Ablation ◽  
Ionic Species ◽  
Mass Spectrometric ◽  
Quadrupole Mass ◽  
Time Resolved ◽  
Ambient Oxygen

Pulsed laser ablation of TiO2 at 355 nm and 532 nm has been investigated using an angleand time-resolved quadrupole mass spectrometric technique. The major ablated species include O (m/e = 16), O2 (m/e = 32), Ti (m/e = 48), TiO (m/e = 64) and TiO2 (m/e = 80). The time-of-flight (TOF) spectra of ablated species are measured for the ionic and neutral ablated species, and they can be fitted by a Maxwell – Boltzmann (M – B) distribution with a center-of-mass velocity. The measured angular distributions of the ionic species (O+ and Ti+) and the neutral species (O and Ti) can be fitted with cos⁡nθ and a cos⁡θ + (1−a)cos⁡nθ, respectively. In addition, a continuous wave oxygen molecular beam is introduced into the ablated plume, and the enhancement of the signal intensities of TiO is observed. It implies that the ablated Ti atoms/ions species can react with ambient oxygen molecules in the gas phase. In the meanwhile, the physicochemical mechanism of pulsed laser ablation of TiO2 is discussed.

Sign in / Sign up

Export Citation Format

Share Document