Yanchun Yin

High-efficiency optical parametric chirped-pulse amplifier in BiB 3 O 6 for generation of 3 mJ, two-cycle, carrier-envelope-phase-stable pulses at 1.7 μm

We produce a 3 mJ, two-cycle (11.4 fs), 1 kHz, carrier-envelope phase (CEP)-stable laser source at 1.7 μm via a three-stage Ti:sapphire-pumped optical parametric chirped-pulse amplifier in BiB3O6. We achieve a pump-to-signal conversion efficiency of 18% in the last stage, which is, to the best of our knowledge, the highest yet achieved for near-octave bandwidth amplification. A f-to-2f measurement shows a CEP instability of 165 mrad over 1 h. This is an ideal light source for generating isolated attosecond pulses in the soft x-ray region.

Polarization gating of high harmonic generation in the water window

High harmonic spectrum from 50-350 eV is achieved via polarization gating technique using an OPCPA laser at 1.7 μm. The driving lasers carrier-envelope phase influence on the high harmonic generation yield indicates that isolated attosecond pulses are generated.

53-attosecond X-ray pulses reach the carbon K-edge

The motion of electrons in the microcosm occurs on a time scale set by the atomic unit of time—24 attoseconds. Attosecond pulses at photon energies corresponding to the fundamental absorption edges of matter, which lie in the soft X-ray regime above 200 eV, permit the probing of electronic excitation, chemical state, and atomic structure. Here we demonstrate a soft X-ray pulse duration of 53 as and single pulse streaking reaching the carbon K-absorption edge (284 eV) by utilizing intense two-cycle driving pulses near 1.8-μm center wavelength. Such pulses permit studies of electron dynamics in live biological samples and next-generation electronic materials such as diamond.Isolated attosecond pulses are produced using high harmonic generation and sources of these pulses often suffer from low photon flux in soft X-ray regime. Here the authors demonstrate efficient generation and characterization of 53 as pulses with photon energy near the water window.

High-energy two-cycle pulses at 3.2 μm by a broadband-pumped dual-chirped optical parametric amplification.

A design for efficient generation of mid-infrared pulses at 3.2 μm is presented, which is based on numerical simulations of the broadband-pumped dual-chirped optical parametric amplification (DC-OPA) in LiNbO3 doped with 5 mol.% MgO (MgO:LiNbO3). The broadband seed can be generated by difference frequency generation in KTA using spectrally-broadened Ti:Sapphire lasers. The broad DC-OPA phase-matching bandwidth-spanning from 2.4 μm to 4.0 μm-is achieved by chirping both the broadband Ti:Sapphire pump pulses and the seed pulses in such a way that the individual temporal slice of pump spectrum is able to phase match that of seed spectrum. This phase matching scheme allows the use of longer crystals without gain narrowing or loss of conversion efficiency. The theoretical conversion efficiency from the pump to the idler reaches 19.1 %, enabling generation of a few hundred mJ of mid-IR energy with an available large-aperture MgO:LiNbO3 crystal. Furthermore, the commercially available acousto-optic programmable dispersive filter (AOPDF) ensures compression of such a broad bandwidth down to 20 fs (two optical cycles at 3.2 μm).

Laser waveform control of extreme ultraviolet high harmonics from solids

Solid-state high-harmonic sources offer the possibility of compact, high-repetition-rate attosecond light emitters. However, the time structure of high harmonics must be characterized at the sub-cycle level. We use strong two-cycle laser pulses to directly control the time-dependent nonlinear current in single-crystal MgO, leading to the generation of extreme ultraviolet harmonics. We find that harmonics are delayed with respect to each other, yielding an atto-chirp, the value of which depends on the laser field strength. Our results provide the foundation for attosecond pulse metrology based on solid-state harmonics and a new approach to studying sub-cycle dynamics in solids.

High-harmonic generation in amorphous solids

High-harmonic generation in isolated atoms and molecules has been widely utilized in extreme ultraviolet photonics and attosecond pulse metrology. Recently, high-harmonic generation has been observed in solids, which could lead to important applications such as all-optical methods to image valance charge density and reconstruct electronic band structures, as well as compact extreme ultraviolet light sources. So far these studies are confined to crystalline solids; therefore, decoupling the respective roles of long-range periodicity and high density has been challenging. Here we report the observation of high-harmonic generation from amorphous fused silica. We decouple the role of long-range periodicity by comparing harmonics generated from fused silica and crystalline quartz, which contain the same atomic constituents but differ in long-range periodicity. Our results advance current understanding of the strong-field processes leading to high-harmonic generation in solids with implications for the development of robust and compact extreme ultraviolet light sources.Although higher harmonic generation from solids has become of interest in many fields, its observation is typically limited to crystalline solids. Here, the authors demonstrate that higher harmonics can be generated from amorphous solids.

Towards Terawatt Sub-Cycle Long-Wave Infrared Pulses via Chirped Optical Parametric Amplification and Indirect Pulse Shaping.

We present an approach for both efficient generation and amplification of 4–12 μm pulses by tailoring the phase matching of the nonlinear crystal Zinc Germanium Phosphide (ZGP) in a narrowband-pumped optical parametric chirped pulse amplifier (OPCPA) and a broadband-pumped dual-chirped optical parametric amplifier (DC-OPA), respectively. Preliminary experimental results are obtained for generating 1.8–4.2 μm super broadband spectra, which can be used to seed both the signal of the OPCPA and the pump of the DC-OPA. The theoretical pump-to-idler conversion efficiency reaches 27% in the DC-OPA pumped by a chirped broadband Cr2+:ZnSe/ZnS laser, enabling the generation of  Terawatt-level 4–12 μm pulses with an available large-aperture ZGP. Furthermore, the 4–12 μm idler pulses can be compressed to sub-cycle pulses by compensating the tailored positive chirp of the idler pulses using the bulk compressor NaCl, and by indirectly controlling the higher-order idler phase through tuning the signal (2.4–4.0 μm) phase with a commercially available acousto-optic programmable dispersive filter (AOPDF). A similar approach is also described for generating high-energy 4–12 μm sub-cycle pulses via OPCPA pumped by a 2 μm Ho:YLF laser.

Generation of octave-spanning mid-infrared pulses from cascaded second-order nonlinear processes in a single crystal

We report on experimental generation of a 6.8 μJ laser pulse spanning from 1.8 to 4.2 μm from cascaded second-order nonlinear processes in a 0.4-mm BiB3O6 (BIBO) crystal. The nonlinear processes are initiated by intra-pulse difference frequency generation (DFG) using spectrally broadened Ti:Sapphire spectrum, followed by optical parametric amplification (OPA) of the DFG pulse. The highest energy, 12.6 μJ, is achieved in a 0.8-mm BIBO crystal with a spectrum spanning from 1.8 to 3.5 μm. Such cascaded nonlinear processes are enabled by the broadband pump and the coincident phase matching angle of DFG and OPA. The spectrum is initiated from the DFG process and is thus expected to have passive stable carrier-envelope phase, which can be used to seed either a chirped pulse amplifier (CPA) or an optical parametric chirped pulse amplifier (OPCPA) for achieving high-energy few-cycle mid-infrared pulses. Such cascaded second-order nonlinear processes can be found in many other crystals such as KTA, which can extend wavelengths further into mid-infrared. We achieved a 0.8 μJ laser pulse spanning from 2.2 to 5.0 μm in KTA.

Erratum: 53-attosecond X-ray pulses reach the carbon K-edge

Nature Communications8:186 10.1038/s41467-017-00321-0 (2017); Article published online: 4 August 2017