A critical component for all high-power laser systems that is particularly susceptible to laser damage is the antireflective coating, which maximizes energy transmission and minimizes scattered and stray light. We demonstrate the ability to generate substrate-engraved nanostructured surfaces (NS) for scalable and designable antireflective (AR) coatings that are monolithic to the substrate and can handle peak power levels comparable to the bulk material. Experimentally measured reflectance from these fabricated structures has validated our effective index theory-based transmission matrix model, demonstrating the designability of the AR properties. Upon exposure to sufficiently high fluences, a new mode of damage, nanostructured surface damage, has been observed and is likely the result of thermally driven material reflow accompanied by plasma initiation on the nanostructured surface. At 1053 nm, nanostructured surface damage onsets at 39 J / c m 2 with sample cleaning and 74 J / c m 2 after laser conditioning—very close to the reference substrate at 81 J / c m 2 . At 351 nm we show damage onset of 30 J / c m 2 , with reference substrate material damage onset of 47 J / c m 2 . Therefore, damage is close to the bulk material and represents an improvement with respect to other methods. The nanostructured surfaces were found to be mechanically durable and able to withstand cleaning procedures with sonication. Under normal incidence mechanical testing with a 200 µm radius indenter tip, the AR performance of these nanostructured surfaces was minimally impacted at pressures orders of magnitude higher than an average fingerprint pressure—indicating that incidental handling contact will not affect NS structures. Mechanical damage is attributed to plastic compression, not fracturing of the NS features. We demonstrate for the first time, to the best of our knowledge, that NS AR coatings, despite being rich in etched surface features, can tolerate laser fluences comparable to unprocessed optical surfaces. Furthermore, laser-damage features of NS indicate a unique non-growing failure mode whereby following absorption the featureless damage site does not precipitate future damage growth, reducing considerably the burdens for managing optics processing in high-power laser systems.

We have used photon pair correlations generated via spontaneous parametric downconversion (SPDC) to measure the fluorescence lifetime of the organic dye rhodamine 6 G, demonstrating that fluorescence lifetime measurements can be achieved using a continuous wave (CW) laser, without pulsed or modulated lasers. Our entangled photon method, quantum fluorescence lifetime (Q-FL) measurements, uses one photon to excite fluorescence and the resulting fluorescence photon is timed and referenced to the arrival time of the other entangled photon. Thus, we can exploit the short timescale of photon pair correlations to conduct experiments that are typically carried out with pulsed lasers and we show that the inherent timing of the photons is fast enough to resolve the nanosecond scale fluorescence lifetime of the sample. This measurement paves the way towards using the time correlations of entangled photons for fluorescence imaging; capitalizing on the presence of fast, sub-100 ps correlations that have not been demonstrated classically.