Elliptically polarized high-order harmonics opens a path toward the study of ultrafast dynamics in circular dichroism of magnetic materials, chiral molecules, and electronic spin motion. Recently, efficient high-order harmonic generation with controllable ellipticity has attracted considerable attention in experiment and theory. Here, we experimentally demonstrate a scenario using cross-linearly-polarized two-color fields consisting of a fundamental field and its second harmonic (SH). Through adjusting the relative phase, crossing angle, and intensity ratio of the cross-linearly-polarized two-color field, we obtain ellipticity-tunable high-order harmonics, with ellipticity up to $\varepsilon =0.73$. Meanwhile, the elliptically polarized high-order harmonics preserve high efficiency. Furthermore, when the intensity of the SH field is stronger than that of the fundamental field, the even order harmonics will become several times stronger than the odd order harmonics with opposite helicity.

In this work, we present an experimental study on the acoustic vibrations of ZnO nanoparticles array with different concentration of Ga dopings by using femtosecond pump-probe technique. The Ga-doped ZnO (GZO) nano-triangle particles with the sizes of 190, 232 and 348 nm are fabricated by nanosphere lithography and pulsed laser deposition method. The result indicates that the frequency of acoustic vibrations of GZO nanoparticles decrease as the Ga-concentration is increased. Importantly, the vibration period of the GZO nanoparticles at the same Ga doping concentration show a nonlinear increase as the nanoparticle size is increased, which is different from the common linear dependency in undoped ZnO nanoparticles. It may be attributed to the crystal structure distortion and elastic characteristics variation due to Ga doping, and the elastic modulus at 7.3% Ga doping is decreased by 30%–60% for GZO nanoparticles with different sizes. The study can be very helpful for evaluating the crystal structure distortion and elastic characteristics of doped nano-materials with optical methods. Besides, it can offer a complementary method of thermal management in ZnO based optoelectronic devices.

We theoretically demonstrate the control of the polarization direction of isolated attosecond pulses (IAPs) with inhomogeneous two-color fields synthesized by an 800-nm fundamental pulse and a 2000-nm control pulse having crossed linear polarizations. The results show that by using the temporally and spatially shaped field, the high-order harmonic generation (HHG) process can be efficiently controlled. An ultra-broad supercontinuum ranging from 150th to 400th harmonics which covers the water window region is generated. Such a supercontinuum supports the generation of a 64-as linearly polarized IAP, whose polarization direction is at about 45° with respect to the x axis. Moreover, we analyze the influence of the inhomogeneity parameters and the relative angle of the fundamental and control pulses on the IAP generation. It is shown that the polarization direction of the IAP can rotate in a wide range approximately from 8° to 90° relative to the x axis when the inhomogeneity parameters and the relative angle vary.

We theoretically investigate high-order harmonic generation from nanowire in inhomogeneous laser field. By solving the time-dependent Schrödinger equation, the simulated harmonic spectrum exhibits a double-plateau structure. The cutoff of the second plateau is extended and the intensity of the high-order harmonics in the second plateau is increased by about two to three orders of magnitude compared with that from the homogeneous laser field. Moreover, we analyze the influence of the inhomogeneous laser field polarization orientation to the nanowire. It is shown that the intensity of the high-order harmonics in the second plateau can be effectively controlled by varying the inhomogeneity parameter and the laser field polarization orientation to the nanowire. These phenomena are attributed to the time-dependent population of the electron, which has a strong relevance with the intensity of the harmonic.