Related Experiment Video
Updated: Jan 25, 2026

20 mJ, 1 ps Yb:YAG Thin-disk Regenerative Amplifier
Published on: July 12, 2017
Fiber-amplifier-pumped, 1-MHz, 1-µJ, 2.1-µm, femtosecond OPA with chirped-pulse DFG front-end
Abstract:
High-repetition-rate, high-power, few-cycle mid-infrared lasers with carrier-envelope phase (CEP) stabilization are ideal driving sources for studying strong-field nonlinear processes, such as strong-field driven electron emission, solid-state high-harmonic generation, and nonlinear microscopy. Here, we report on a 1-MHz, 1-μJ, femtosecond, 2.1-µm optical parametric amplifier (OPA), pumped by a Yb-doped fiber chirped-pulse amplifier (CPA) and seeded by a chirped-pulse difference-frequency generation (DFG) front-end providing positively chirped 2.1-μm signal pulses. The home-built multi-stage 1030-nm Yb-doped fiber CPA pump laser generates >55-μJ near-transform-limited (245-fs) pulses at 1 MHz repetition rate using a novel 4-pass all-fiber stretcher/front-end for careful dispersion/spectral management. The chirped-pulse DFG scheme is achieved by wave-mixing the 1030 nm pump pulse with a dispersive wave at 645-735 nm generated in a photonic crystal fiber, allowing passive CEP stability of the 2.1-µm pulses. The 2.1-μm pulse is amplified to 1 μJ in a two-stage dispersion-managed optical parametric amplifier (OPA) with a pump energy of ~21 μJ resulting in 95-fs pulses with nice beam profile without additional pulse compression. Multi-μJ, sub-30 fs pulses can be obtained at full pump energy and additional dispersion compensation. The fiber-amplifier-based mid-infrared OPA can be directly applied to high-harmonic generation in solids and optical-field-driven nanophotonic devices and is a compact front-end for a future high-power, high-repetition-rate, long wavelengths CEP-stabilized source for gas-phase high-order harmonic generation.
More Related Videos
Related Concept Videos
SN1 Reaction: Stereochemistry
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
SN1 Reaction: Kinetics
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
SN1 Reaction: Mechanism
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Predicting Products: SN1 vs. SN2
With increased substitution on the alkyl halide,...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...

