RESUMEN
Molybdenum carbides (MoC and Mo2C) are being reported for various applications, for example, catalysts for sustainable energies, nonlinear materials for laser applications, protective coatings for improving tribological performance, and so on. A one-step method for simultaneously fabricating molybdenum monocarbide (MoC) nanoparticles (NPs) and MoC surfaces with a laser-induced periodic surface structure (LIPSS) was developed by using pulsed laser ablation of a molybdenum (Mo) substrate in hexane. Spherical NPs with an average diameter of 61 nm were observed by scanning electron microscopy. The X-ray diffraction pattern and electron diffraction (ED) pattern results indicate that a face-centered cubic MoC was successfully synthesized for the NPs and on the laser-irradiated area. Notably, the ED pattern suggests that the observed NPs are nanosized single crystals, and a carbon shell was observed on the surface of MoC NPs. The X-ray diffraction pattern of both MoC NPs and LIPSS surface indicates the formation of FCC MoC, agreeing with the results of ED. The results of X-ray photoelectron spectroscopy also showed the bonding energy attributed to Mo-C, and the sp2-sp3 transition was confirmed on the LIPSS surface. The results of Raman spectroscopy have also supported the formation of MoC and amorphous carbon structures. This simple synthesis method for MoC may provide new possibilities for preparing Mo x C-based devices and nanomaterials, which may contribute to the development of catalytic, photonic, and tribological fields.
RESUMEN
In this study, we developed a one-step method for fabricating hydrophobic surfaces on copper (Cu) substrates. Cuprous oxide (Cu2O) with low free energy was successfully formed after low-fluence laser direct irradiation. The formation of Cu2O enhanced the hydrophobicity of the Cu substrate surface, and the contact angle linearly increased with the proportion of Cu2O. The Cu2O fabricated by low-fluence laser treatment showed the same crystal plane orientation as the pristine Cu substrate, implying an epitaxial growth of Cu2O on a Cu substrate.
RESUMEN
A laser-fabricated metallic resonator based on a double-slit array (DSA) is numerically and experimentally demonstrated at terahertz frequencies. Such free-standing resonators achieve a sharp resonance with high quality (Q) factor, arising from a distortion of symmetry-protected bound states in the continuum (BIC). By breaking the structural symmetry of DSAs, the BIC with infinite Q-factor can be transformed into quasi-BICs, and the Q-factors decrease gradually as the asymmetry parameter increases. We analyzed the influence of the imperfection in experimental samples such as the round edge and the trapezoid shape on the transmission properties of DSAs. Different from the DSAs composed of ideal perfect electrical conductors, copper DSAs show lower Q-factor because of the Ohmic loss. The effect of metal thickness on the quasi-BICs for DSAs is also investigated. Results exhibit that thinner resonators can achieve sharper quasi-BICs. These findings suggest that such metallic resonators with high Q-factors have great potential for practical applications in electromagnetic wave filtering and biomolecular sensing.
RESUMEN
The induction of surface cleavage along the crystalline structure of a zinc oxide substrate (plane orientation: 0001) by femtosecond laser pulses (wavelength: 1030 nm) has been reported; a scanning electron microscope image of the one-pulse (pulse energy: 6-60 µJ) irradiated surface shows very clear marks from broken hexagons. This cleavage process differs from the general laser-induced melt process observed on the surfaces of narrower-bandgap semiconductors and other metal materials. This phenomenon is discussed using a multi-photon absorption model, and the pulse-energy dependence of the cleavage depth (less than 3 µm) is quantitatively analyzed. Laser-induced cleavage is found not to occur under multi-pulse irradiation; when more than four pulses are irradiated upon the same spot, the general laser-induced melt process becomes dominant. This cleavage-melt shift is considered to be caused by the enhancement of absorption due to the initial pulses, which is supported by our measurement of cathodoluminescence.
