Dynamical systems based on the interplay of nonlinear feedback mechanisms are ubiquitous in nature [1][2][3][4][5] . Well-understood examples from photonics include mode locking 6 and a broad class of fractal optics 7 , including self-similarity 8 . In addition to the fundamental interest in such systems, fascinating technical functionalities that are difficult or even impossible to achieve with linear systems can emerge naturally from them 7 if the right control tools can be applied. Here, we demonstrate a method that exploits positive nonlocal feedback to initiate, and negative local feedback to regulate, the growth of ultrafast laser-induced metal-oxide nanostructures with unprecedented uniformity, at high speed, low cost and on non-planar or flexible surfaces. The nonlocal nature of the feedback allows us to stitch the nanostructures seamlessly, enabling coverage of indefinitely large areas with subnanometre uniformity in periodicity. We demonstrate our approach through the fabrication of titanium dioxide and tungsten oxide nanostructures, but it can also be extended to a large variety of other materials.The fabrication of nanostructures on surfaces is of paramount importance in nanotechnology and materials science 9 . There are several established techniques, including photolithography, electron-beam lithography, imprint lithography 10 and laser interference lithography 11 , as well as non-conventional approaches such as selfassembly 12 and direct laser writing 13 . These techniques require either high-cost, complex systems or offer limited flexibility. An alternative flexible and potentially very low-cost method is laserinduced periodic surface structuring (LIPSS). The first observation of LIPSS dates back to 1965 14 . However, after almost 50 years and a large body of published work that has demonstrated LIPSS on various metals, semiconductors and glasses [15][16][17][18][19] , the method has not found widespread use due to the stubborn problem of quality control 18,19 .Despite the evident role of self-assembly in the LIPSS process, uniformity and long-range order remain poor, a problem we identified as originating from the fact that the structures are initiated from multiple seed locations concurrently and independently, thereby producing an irregular pattern. Because the process is irreversible, without self-correction, these irregularities become frozen. Our solution to this relies on carefully exploiting feedback mechanisms to tightly regulate the formation of nanostructures induced by ultrashort pulses. This process can be summarized in three steps.(1) The laser beam, with a peak intensity close to the ablation threshold for titanium, is focused on a titanium surface, where it is scattered by existing nanostructures or any surface defects 15 . The interference of the scattered and incident fields leads to intensity variations in the immediate neighbourhood of the scattering point. (2) At points where the threshold intensity for ablation is exceeded, titanium reacts rapidly with O 2 from the air, form...

We have synthesized a series of chalcogenide glasses from the As-S-Se system that is designed to have strong nonlinearities. Measurements reveal that many of these glasses offer optical Kerr nonlinearities greater than 400 times that of fused silica at 1.25 and 1.55mum and figures of merit for all-optical switching greater than 5 at 1.55mum .

Silicon is an excellent material for microelectronics and integrated photonics1–3 with untapped potential for mid-IR optics4. Despite broad recognition of the importance of the third dimension5,6, current lithography methods do not allow fabrication of photonic devices and functional microelements directly inside silicon chips. Even relatively simple curved geometries cannot be realised with techniques like reactive ion etching. Embedded optical elements, like in glass7, electronic devices, and better electronic-photonic integration are lacking8. Here, we demonstrate laser-based fabrication of complex 3D structures deep inside silicon using 1 µm-sized dots and rod-like structures of adjustable length as basic building blocks. The laser-modified Si has a different optical index than unmodified parts, which enables numerous photonic devices. Optionally, these parts are chemically etched to produce desired 3D shapes. We exemplify a plethora of subsurface, i.e., “in-chip” microstructures for microfluidic cooling of chips, vias, MEMS, photovoltaic applications and photonic devices that match or surpass the corresponding state-of-the-art device performances.

A series of experiments aimed at determining the maximum pulse energy that can be produced by a femtosecond fiber laser is reported. Exploiting modes of pulse propagation that avoid wave breaking in a Yb fiber laser allows pulse energies up to 14 nJ to be achieved. The pulses can be dechirped to sub-100-fs duration to produce peak powers that reach 100 kW. The limitations to the maximum pulse energy are discussed.

We report the generation of 6-nJ chirped pulses from a mode-locked Yb fiber laser at 1.03 micrometre. A linear anomalous-dispersion segment suppresses wave-breaking effects of solitonlike pulse shaping at high energies. The dechirped pulse duration is 50 fs, and the energy is 5 nJ. This laser produces twice the pulse energy and average power, and approximately five times the peak power, of the previous best mode-locked fiber laser. It is to our knowledge the first fiber laser that directly offers performance similar to that of solid-state lasers such as Ti:sapphire.