
The approach enables rapid, high‑throughput measurement of ultrafast electron dynamics, accelerating superconductor research and device engineering while improving data reliability by removing ambiguous fitting steps.
The ability to resolve electronic thermalisation on sub‑picosecond scales is a cornerstone of modern quantum‑material research. Traditional pump‑probe analyses rely on multi‑parameter fitting of transient reflectivity, a process that can obscure physical insight and introduce user bias. The newly proposed nematic response function model (NRFM) sidesteps these pitfalls by defining the nematic signal as the difference between orthogonal polarisation channels, allowing the characteristic extremum to serve as a direct time marker. Coupled with the established two‑temperature model, the approach delivers a fit‑free pathway to quantify electron‑electron relaxation.
Applying the NRFM to FeSeTe and Ba(Fe₀.₉₂Co₀.₀₈)₂As₂ thin films, the team extracted electronic thermalisation constants ranging from 110 fs to 230 fs, values that align closely with conventional two‑temperature model fits. Crucially, the method also resolves directional anisotropy inherent to nematic order, offering a nuanced view of quasiparticle scattering that was previously masked by global fitting routines. This level of precision enhances our understanding of electron‑phonon coupling in iron‑based superconductors and informs theories of high‑temperature superconductivity.
Beyond iron‑based systems, the NRFM framework is readily transferable to any material exhibiting electronic nematicity, from twisted bilayer graphene to cuprate families. By eliminating labor‑intensive fitting, researchers can perform high‑throughput surveys of doping, temperature, or strain effects, accelerating the discovery of compounds with optimal ultrafast response for superconducting electronics or terahertz devices. Future work will likely focus on integrating the technique with broadband probe schemes and extending it to heterostructures, positioning the NRFM as a standard tool in the ultrafast spectroscopy toolbox.
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