Advanced ultrafast spectroscopy

Ultrafast spectroscopy with few-femtosecond dispersive waves

We collaborate with multiple world-renowed ultrafast spectroscopy groups on the use of our light-source technologies for new discovery science. In particular, the use of our HISOL concept is one of the best ways to get bright few-femtosecond pulses tunable across the vacuum and deep ultraviolet, and we are installing HISOL systems in research facilities and research groups worldwide.

Transient low-energy photoelectron signal extracted from time-resolved photoelectron imaging in the lab of Prof Dave Townsend at Heriot-Watt University. The pump pulse is a ~6-fs deep-ultraviolet dispersive wave and the probe pulse is a ~10-fs infrared pulse. Adpated from [Jackson et al.](https://www.nature.com/articles/s41467-025-58895-z)
Transient low-energy photoelectron signal extracted from time-resolved photoelectron imaging in the lab of Prof Dave Townsend at Heriot-Watt University. The pump pulse is a ~6-fs deep-ultraviolet dispersive wave and the probe pulse is a ~10-fs infrared pulse. Adpated from Jackson et al.

Few-femtosecond dispersive waves can be combined with any number of other ultrafast light sources, from short infrared pulses to attosecond x-rays. We are also working to integrate HISOL sources with major facilities, such as x-ray free-electron lasers like LCLS and the European XFEL.

Attosecond x-ray beamline in the lab of Prof Jon Marangos at Imperial College London. Here, attosecond pulses generated *via* high-harmonic generation are combined with ultraviolet and visible dispersive waves to enable time-resolved x-ray spectroscopy. Adpated from [Lee et al.](ttps://opg.optica.org/optica/abstract.cfm?uri=optica-11-9-1320)
Attosecond x-ray beamline in the lab of Prof Jon Marangos at Imperial College London. Here, attosecond pulses generated via high-harmonic generation are combined with ultraviolet and visible dispersive waves to enable time-resolved x-ray spectroscopy. Adpated from Lee et al.

In our own laboratory, we have demonstrated the use of ultrabroadband self-compression probe pulses in combination with few-femtosecond resonant dispersive waves in studying condensed matter physics with unprecedented time resolution and bandwidth. This approach has also found applications in transient absorption spectroscopy of photochemical processes in the liquid phase.

Measured delay-dependent differential reflectivity of a thin-film sample of vanadium dioxide. The pump pulse is a ~5-fs duration resonant dispersive wave at 610 nm and the probe is a continuum spanning 210-2500 nm, generated by soliton self-compression. Adpated from [Brahms et al.](https://www.nature.com/articles/s41467-025-58895-z)
Measured delay-dependent differential reflectivity of a thin-film sample of vanadium dioxide. The pump pulse is a ~5-fs duration resonant dispersive wave at 610 nm and the probe is a continuum spanning 210-2500 nm, generated by soliton self-compression. Adpated from Brahms et al.

FASTER: Ultrabroadband optical attosecond spectroscopy enabled by soliton self-compression

The FASTER project, led by Christian Brahms, aims to bring attosecond time resolution to ultrafast spectroscopy experiments in the optical region of the electromagnetic spectrum—the ultraviolet, visible and infrared. In contrast to extreme-ultraviolet attosecond science, which was recognised with the Nobel Prize in Physics 2023, this will allow us to study ultrafast dynamics entirely with non-ionising radiation and without resorting to strong-field excitation or probing. We will create the required optical attosecond pulses by building on the work of the HISOL project. With tailored soliton dynamics in hollow-core waveguides, we will transform femtosecond pulses in attosecond ones. These will be then be used in ultrabroadband optical attosecond spectroscopy experiments on a variety of samples, starting with condensed-matter targets.