The measurement and control of light field oscillations enable the study of ultrafast phenomena on sub-cycle time scales. Electro-optic sampling (EOS) is a powerful field characterization approach, in terms of both sensitivity and dynamic range, but it has not reached beyond infrared frequencies. Here, we show the synthesis of a sub-cycle infrared-visible pulse and subsequent complete electric field characterization using EOS. The sampled bandwidth spans from 700 nm to 2700 nm (428 to 110 THz). Tailored electric-field waveforms are generated with a two-channel field synthesizer in the infrared-visible range, with a full-width at half-maximum duration as short as 3.8 fs at a central wavelength of 1.7 µm (176 THz). EOS detection of the complete bandwidth of these waveforms extends it into the visible spectral range. To demonstrate the power of our approach, we use the sub-cycle transients to inject carriers in a thin quartz sample for nonlinear photoconductive field sampling with sub-femtosecond resolution.
These authors contributed equally to this work.The development of high-energy, high-power, multi-octave light-transients is currently subject of intense research driven by emerging applications in attosecond spectroscopy and coherent control. We report on a phase-stable, multi-octave source based on a Yb:YAG amplifier for light-transient generation. We demonstrate the amplification of a two-octave spectrum to 25 µJ of energy in two broadband amplification channels and their temporal compression to 6 fs and 18 fs at 1 µm and 2 µm, respectively. In this scheme due to the intrinsic temporal synchronization between the pump and seed pulses, the temporal jitter is restricted to long-term drift. We show that the intrin-1 arXiv:1911.00545v1 [physics.optics] 1 Nov 2019 sic stability of the synthesizer allows for sub-cycle detection of an electric field at 0.15 PHz. The complex electric field of the 0.15 PHz pulses and their freeinduction decay after interaction with water molecules are resolved by electrooptic sampling over 2 ps. The scheme is scalable in peak-and average-power.
TeaserWe report on a novel source for generating high energy, sub-cycle pulses based on a Yb thindisk laser.
Figure 4. a) EOS (in red) and b) LPS (in blue) spectral response functions calculated with different GDD values applied to the VIS-UV pulse. c) EOS response calculated for a compressed VIS-UV pulse and different crystal thicknesses.
We report on a simple scheme to generate broadband, μJ pulses centered at 2.1 μm with an intrinsic carrier-envelope phase (CEP) stability from the output of a Yb:YAG regenerative amplifier delivering 1-ps pulses with randomly varying CEP. To the best of our knowledge, the reported system has the highest optical-to-optical efficiency for converting 1-ps, 1 μm pulses to CEP stable, broadband, 2.1 μm pulses. The generated coherent light carries an energy of 5.4 μJ, at 5 kHz repetition rate, that can be scaled to higher energy or power by using a suitable front end, if required. The system is ideally suited for seeding broadband parametric amplifiers and multichannel synthesizers pumped by picosecond Yb-doped amplifiers, obviating the need for active timing synchronization. Alternatively, this scheme can be combined with high-power oscillators with tens of μJ energy to generate CEP stable, multioctave supercontinua, suitable for field-resolved and time-resolved spectroscopy.
Access to subtle ultrafast effects of light-matter interaction often requires highly sensitive field detection schemes. Electro-optic sampling, being an exemplary technique in this regard, lacks high sensitivity in an imaging geometry. We demonstrate a straightforward method to significantly improve the contrast of electric field images in spatially resolved electro-optic sampling. A thin-film polarizer is shown to be an effective tool in enhancing the sensitivity of the electro-optic imaging system, enabling an adjustment of the spectral response. We show a further increase of the signal-to-noise ratio through the direct control of the carrier envelope phase of the imaged field.
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