We introduce a method for direct patterning of Ni electrodes through selective laser direct writing (LDW) of NiO nanoparticle (NP) ink. High-resolution Ni patterns are generated from NiO NP thin films by a vacuum-free, lithography-free, and solution-processable route. In particular, a continuous wave laser is used for the LDW reductive sintering of the metal oxide under ambient conditions with the aid of reducing agents in the ink solvent. Thin (∼ 40 nm) Ni electrodes of glossy metallic surfaces with smooth morphology and excellent edge definition can be fabricated. By applying this method, we demonstrate a high transmittance (>87%), electrically conducting panel for a touch screen panel application. The resistivity of the Ni electrode is less than an order of magnitude higher compared to that of the bulk Ni. Mechanical bending test, tape-pull test, and ultrasonic bath test confirm the robust adhesion of the electrodes on glass and polymer substrates.

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This work is concerned with the kinetics of laser-induced reductive sintering of nonstoichiometric crystalline nickel oxide (NiO) nanoparticles (NPs) under ambient conditions. The mechanism of photophysical reductive sintering upon irradiation using a 514.5 nm continuous-wave (CW) laser on NiO NP thin films has been studied through modulating the laser power density and illumination time. Protons produced due to hightemperature decomposition of the solvent present in the NiO NP ink, oxygen vacancies in the NiO NPs, and electronic excitation in the NiO NPs by laser irradiation all affect the early stage of the reductive sintering process. Once NiO NPs are reduced by laser irradiation to Ni, they begin to coalesce, forming a conducting material. In situ optical and electrical measurements during the reductive sintering process take advantage of the distinct differences between the oxide and the metallic phases to monitor the transient evolution of the process. We observe four regimes: oxidation, reduction, sintering, and reoxidation. A characteristic time scale is assigned to each regime.

The transient pressure generated by the interaction of short-pulsed laser light with the liquid–solid interface is studied quantitatively. A KrF excimer laser beam of tens of nanoseconds pulse duration irradiates water on a solid surface and induces rapid thermal expansion and explosive vaporization. The pressure pulses launched into water by such processes are detected experimentally by the photoacoustic probe beam deflection method and a broadband piezoelectric transducer. The peak intensities of the traveling pressure wave measured by these two methods are compared with the theoretical thermoelastic predictions. The measurements show that a compressional pressure wave packet is radiated from the water-solid interface with the peak intensity of the order of 1 MPa at laser fluences up to about 100 mJ/cm2. Simultaneous monitoring of the bubble growth kinetics by the optical specular reflectance probe has been performed. It is observed that the pressure generation is enhanced by the bubble expansion in the superheated water for laser fluences exceeding the bubble nucleation thresholds.

Organic light emitting material direct writing is demonstrated based on nanomaterial enabled laser transfer. Through utilization of proper nanoparticle size and type and the laser wavelength choice, a single laser pulse could transfer well-defined and arbitrarily shaped tris-(8-hydroxyquinoline)Al patterns ranging from several microns to millimeter size. The unique properties of nanomaterials allow laser induced forward transfer at low laser energy (0.05 J/cm2) while maintaining good fluorescence. The technique may be well suited for the mass production of temperature sensitive organic light emitting devices.