Two-photon imaging of soliton dynamics
Łukasz A. Sterczewski1,∗, and Jarosław Sotor1
1Faculty of Electronics, Photonics and Microsystems, Wroclaw University of Science and Technology, Wyb.
Wyspianskiego 27, 50-370 Wroclaw, Poland
∗e-mail: lukasz.sterczewski@pwr.edu.pl
Optical solitary waves (solitons) that interact in a non-
linear system can bind and form a structure similar to a
molecule. The rich dynamics of this process have created
a demand for rapid spectral characterization to deepen the
understanding of soliton physics with many practical impli-
cations. Here, we demonstrate stroboscopic, two-photon
imaging of soliton molecules (SM) with completely unsyn-
chronized lasers, where the wavelength and bandwidth
constraints are considerably eased compared to conven-
tional imaging techniques. Two-photon detection enables
the probe and tested oscillator to operate at completely
different wavelengths, which permits mature near-infrared
laser technology to be leveraged for rapid SM studies of
emerging long-wavelength laser sources. As a demonstra-
tion, using a 1550 nm probe laser we image the behavior
of soliton singlets across the 1800–2100 nm range, and
capture the rich dynamics of evolving multiatomic SM. This
technique may prove to be an essential, easy-to-implement
diagnostic tool for detecting the presence of loosely-bound
SM, which often remain unnoticed due to instrumental
resolution or bandwidth limitations.
Since the discovery in hydrodynamic systems1, solitary
waves also known as solitons have expanded into diverse
areas of science due to the unique way they analogize mat-
ter and waves. Arguably, a significant fraction of soliton
research has been centered around nonlinear optical sys-
tems such as fibers2or microvavity resonators3,4. This is
because optical solitons do not spread out during propaga-
tion and exhibit robustness against perturbations; there-
fore they frame the core concept in optical pulse genera-
tion. Solitons also have the striking ability to form a stable
bond between pairs or groups referred to as SMs5,6. The
binding force7,8 depends on the atomic spacing τ(tem-
poral separation, TS), while the intramolecular phase ∆ϕ
mostly governs the attraction/repulsion effect. Even more
sophisticated physical systems like molecular complexes9
or molecular crystals10 can form via SM collisions. Despite
advances in mathematical modeling11, the understanding
of these complex inter-soliton interactions still appears to
be in infancy.
The rich landscape of nonlinear dynamics and numer-
ous analogies to condensed-matter physics fuel intensive
research in this field with much focus on studying the
evolution dynamics and transient behavior of SM forma-
tion12,13. It stems from the SM application potential to
optical memories, buffers14, or telecommunication to sur-
pass the limitation of classical binary coding schemes15,16.
In such scenarios, one would like to tailor the SM spac-
ing and phase on demand17,18,19,20 rather than rely on its
uncontrolled organization, which necessitates a thorough
characterization of transient short-lived SM states.
SM characterization techniques differ significantly in
obtainable scan rates. Time-averaged (second-scale, Hz-
rate) SM studies are performed with a first-order inten-
sity autocorrelator (IAC) along with an optical spectrum
analyzer (OSA)21, which are suitable mostly for steady-
state phenomena like stable, tightly-bound SM. The high-
est scan rates (shot-to-shot, sub-GHz) are offered by the
celebrated Dispersive Fourier Transformation (DFT) tech-
nique22,23, which temporally stretches a laser pulse in a
linear dispersive medium (such as optical fiber) to map the
time domain to the frequency domain on a pulse-by-pulse
basis12,13,24,18,25. Unfortunately, beyond the 1–2 µm win-
dow, fiber losses may render this technique impractical.
Also the spectral resolution of the two techniques (typi-
cally ∼GHz) may be insufficient to probe loosely-bound
SMs (TS on the order of ns). A much simpler variant of
this method – direct analysis of laser pulses on an oscil-
loscope without dispersive stretching – completely ignores
the molecular phase and fails to resolve solitons spaced by
ps due to electrical bandwidth limitations.
To fill a niche between the two timescales, recent works
have proposed to adapt the phase-sensitive electric field
cross-correlation (EFXC) technique26 often referred to as
coherent optical sampling27 or dual-comb spectroscopy
(DCS)28 for imaging the dynamics of solitons in microres-
onators3,4. However, high scan rates with EFXC are
obtainable only with multi-GHz repetition-rate sources.
In the case of fiber laser cavities, which constitute a ma-
jority of SM generators, the aliasing (Nyquist) limitation
strongly constraints the observable optical bandwidth
due to sources’ low, MHz repetition rates, and restricts
frame rates to the 10’s–100’s of Hz range. The need
for phase locking between the lasers also adds a layer of
complexity. The greatest difficulty, however, results from
the need of a second, spectrally-matched laser, which may
be impractical to implement at exotic wavelengths.
To bypass these limitations and unlock the kHz- to
sub-MHz rate imaging potential, in this Article we adapt
the non-interferometric intensity cross-correlation (IXC)
technique29 to the problem of dynamic soliton imaging.
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arXiv:2210.09966v1 [physics.optics] 18 Oct 2022