2019
DOI: 10.7567/1347-4065/ab3368
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Femto- and nano-second laser-induced damages in chalcogenide glasses

Abstract: We have studied damaging behaviors in bulk As2Se3, Se and As2S3 glasses using fs and ns laser pulses. Threshold fluence of laser damages markedly varies with excitations and materials. Under sub-gap fs pulses with photon-energy of ħω = 1.6 eV, the threshold in As2S3 is roughly twice that of the other two glasses, and photo-crystallization appears in Se. For ns pulses, all the glasses under bandgap (ħω = 2.3 eV) illumination possess higher thresholds than those under mid-gap (ħω = 1.2 eV) illumination. These ob… Show more

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Cited by 5 publications
(4 citation statements)
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“…Presumably, modification of As 2 S 3 requires higher energies of laser pulses because the As–S chemical bonds are stronger than those of As–Se (260 and 230 kJ/mol, respectively) [ 43 ]. Typically, ablation threshold for As 2 Se 3 was reported to be almost twice less than for As 2 S 3 [ 44 , 45 ].…”
Section: Resultsmentioning
confidence: 99%
“…Presumably, modification of As 2 S 3 requires higher energies of laser pulses because the As–S chemical bonds are stronger than those of As–Se (260 and 230 kJ/mol, respectively) [ 43 ]. Typically, ablation threshold for As 2 Se 3 was reported to be almost twice less than for As 2 S 3 [ 44 , 45 ].…”
Section: Resultsmentioning
confidence: 99%
“…The measured Raman spectra of detonation and HP-HT nanodiamond films show pronounced peaks with frequency shifts of 1329 and 1330 cm −1 , respectively (see Figure 2a). Taking into account the known dependences of the Raman shifts of carbon nanomaterials on the excitation wavelength [53] and the nanoparticle size [54], one can attribute these peaks to nanodiamonds (sp 3 -form of carbon). The decomposition of the spectra presented in Figure 2a shows that the full width at half maximum (FWHM) of diamond lines of HP-HT and detonation nanodiamonds are 8 and 22 cm −1 , respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Thin CuSe/Se films with a thickness of 130 nm and dimensions of 15 35 mm were synthesized on a glass substrate by successive vacuum thermal deposition of Se and Cu, according to the procedure described in one of our previous publications [14]. To stabilize the residual Se [53,54], the synthesized film structure was annealed at a temperature of • for 30 min. As a result, the selenium from an unstable amorphous phase was into a stable polycrystalline trigonal selenium (t-Se).…”
Section: Methodsmentioning
confidence: 99%
“…Thin CuSe/Se films with a thickness of 130 nm and dimensions of 15 × 35 mm were synthesized on a glass substrate by successive vacuum thermal deposition of Se and Cu, according to the procedure described in one of our previous publications [14]. To stabilize the residual Se [53,54], the synthesized film structure was annealed at a temperature of 140 • C for 30 min. As a result, the selenium from an unstable amorphous phase was transformed into a stable polycrystalline trigonal selenium (t-Se).…”
Section: Methodsmentioning
confidence: 99%