Large Stokes shift fast emitters show a negligible reabsorption of their luminescence, a feature highly desirable for several applications such as fluorescence imaging, solar-light managing, and fabricating sensitive scintillating detectors for medical imaging and high-rate high-energy physics experiments. Here we obtain high efficiency luminescence with significant Stokes shift by exploiting fluorescent conjugated acene building blocks arranged in nanocrystals. Two ligands of equal molecular length and connectivity, yet complementary electronic properties, are co-assembled by zirconium oxy-hydroxy clusters, generating crystalline hetero-ligand metal-organic framework (MOF) nanocrystals. The diffusion of singlet excitons within the MOF and the matching of ligands absorption and emission properties enables an ultrafast activation of the low energy emission in the 100 ps time scale. The hybrid nanocrystals show a fluorescence quantum efficiency of ~60% and a Stokes shift as large as 750 meV (~6000 cm−1), which suppresses the emission reabsorption also in bulk devices. The fabricated prototypal nanocomposite fast scintillator shows benchmark performances which compete with those of some inorganic and organic commercial systems.

Nanocrystals of CsPbBr3 have been incorporated in a polystyrene matrix with 1–10% weight filling factors. Samples were characterized with the main focus on their timing capability under soft X-ray irradiation for application as ultrafast scintillation detectors.

The demand for detectors with a time resolution below 100 ps is at the center of research in different fields, from high energy physics to medical imaging. In recent years, interest has grown in nanomaterials that, benefiting from quantum confinement effects, can feature ultra-fast scintillation kinetics and tunable emission. However, standard characterization methods for scintillation properties–relying on radiation sources with an energy range of several hundreds of keV–are not suitable for these materials due to their low stopping power, leading to a slowdown of this R&D line. We present a new method to characterize the time resolution and light output of scintillating materials, using a soft (0–40 keV energy) pulsed X-ray source and optimized high-frequency readout electronics. First, we validated the proposed method using standard scintillators. Then, we also demonstrated the feasibility to measure the time resolution and get an insight into the light output of nanomaterials (InGaN/GaN multi-quantum well and CsPbBr3 perovskite). This technique is, therefore, proposed as a fundamental tool for characterization of nanomaterials and, more in general, of materials with low stopping power to better guide their development. Moreover, it opens the way to new applications where fast X-ray detectors are requested, such as time-of-flight X-ray imaging.