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Tae Won Nam

Publications and source records attributed to Tae Won Nam.

2 recordsLinked to original sources

High Spectral Energy Density All-Fiber Nanosecond Pulsed 1.7 $μ$m Light Source for Photoacoustic Microscopy

We present a high spectral energy density all-fiber nanosecond pulsed 1.7 $μ$m light source specifically designed for photoacoustic microscopy (PAM). The system targets the first overtone absorption of C-H bonds near 1720 nm within the near-infrared-III (NIR-III) window, where lipids exhibit strong optical absorption and tissues benefit from reduced scattering and high permissible fluence. To achieve narrow linewidth, high pulse energy, and high pulse repetition rate (PRR), we developed a master oscillator fiber amplifier architecture based on stimulated Raman scattering. A 1589.80 nm Raman pump and a custom-built narrow-linewidth Raman seed laser were employed to generate spectrally pure 1719.44 nm pulses with an approximately 0.10 nm linewidth. The proposed light source delivers nanosecond pulses of approximately 5 ns with high pulse energy of at least 2.2 $μ$J and tunable PRRs up to 300 kHz, resulting in a spectral energy density of approximately 22 $μ$J/nm, which is significantly higher than that of conventional 1.7 $μ$m light sources. The performance of the NIR-PAM system was validated through resolution testing with a 1951 USAF target, demonstrating a spatial resolution of approximately 4.14 $μ$m and an axial resolution of approximately 85.5 $μ$m. Phantom imaging of CH$_2$-rich polymer films and ex vivo lipid-rich biological tissues confirmed the system's high spatial fidelity and strong contrast for lipid-specific structures. This compact, stable, and spectrally refined light source with high spectral energy density can offer an effective solution for high-resolution, label-free molecular imaging and represents a promising platform for clinical photoacoustic imaging applications involving lipid detection and metabolic disease diagnostics.

physics.optics↗

Template Dissolution Interfacial Patterning of Single Colloids for Nanoelectrochemistry and Nanosensing

Deterministic positioning and assembly of colloidal nanoparticles (NPs) onto substrates is a core requirement and a promising alternative to top down lithography to create functional nanostructures and nanodevices with intriguing optical, electrical, and catalytic features. Capillary-assisted particle assembly (CAPA) has emerged as an attractive technique to this end, as it allows controlled and selective assembly of a wide variety of NPs onto predefined topographical templates using capillary forces. One critical issue with CAPA, however, lies in its final printing step, where high printing yields are possible only with the use of an adhesive polymer film. To address this problem, we have developed a template dissolution interfacial patterning (TDIP) technique to assemble and print single colloidal AuNP arrays onto various dielectric and conductive substrates in the absence of any adhesion layer, with printing yields higher than 98%. The TDIP approach grants direct access to the interface between the AuNP and the target surface, enabling the use of colloidal AuNPs as building blocks for practical applications. The versatile applicability of TDIP is demonstrated by the creation of direct electrical junctions for electro- and photoelectrochemistry and nanoparticle-on-mirror geometries for single particle molecular sensing.

cond-mat.soft↗