Laser-induced optical breakdown by femtosecond pulses is extraordinarily precise when the energy is near threshold. Despite numerous applications, the basis for this deterministic nature has not been determined. We present experiments that shed light on the basic mechanisms of light-matter interactions in this regime, which we term ''optics at critical intensity.'' We find that the remarkably sharp threshold for laser-induced material damage enables the structure or properties of materials to be modified with nanometer precision. Through detailed study of the minimum ablation size and the effects of polarization, we propose a fundamental framework for describing light-matter interactions in this regime. In surprising contrast to accepted damage theory, multiphoton ionization does not play a significant role. Our results also reject the use of the Keldysh parameter in predicting the role of multiphoton effects. We find that the dominant mechanism is Zener ionization followed by a combination of Zener and Zenerseeded avalanche ionization. We predict that the minimum feature size ultimately depends on the valence electron density, which is sufficiently high and uniform, to confer deterministic behavior on the damage threshold even at the nanoscale. This behavior enables nanomachining with high precision, which we demonstrate by machining highly reproducible nanometer-sized holes and grooves in dielectrics.

Two Yb(3+) -doped KY(WO(4))(2) regenerative amplifiers, one end pumped by two 1.6-W single-stripe diodes at 940 nm and the other side pumped by one 20-W diode bar at 980 nm, are demonstrated. When the regenerative amplifiers are injected, 40-muJ , 400-fs and 65-muJ , 460-fs pulses at a 1-kHz repetition rate are obtained following compression from the end- and side-pumped amplifiers, respectively.

Ni/Al nanostructured multilayer foils were machined with femtosecond pulse-length laser irradiation at various fluences. Scanning electron microscopy, back-scattered electron detection, and atomic force microscopy were used to characterize the resulting laser modified regions. We show that material removal at the micron scale is possible with no ignition of a self-propagation reaction emanating from the irradiated areas, a danger minimized by the fact that the extremely short time duration of the pulse produces negligible heat dissipation into the multilayer system. Nevertheless, initial AFM and BSE results give indication that multilayers may be intermixing and reacting locally in areas smaller than the laser beam diameter, though the exact ignition mechanism is still to be determined.