arXiv subjects

Nasim Zarrabi

Publications and source records attributed to Nasim Zarrabi.

4 recordsLinked to original sources

arXiv2026

Roadmap on UV-C photodetectors: materials, applications and industry perspectives

UV-C photodetectors are poised to play an increasingly important role in future photonic technologies, driven by the rapid emergence of UV-C light sources and new wide bandgap semiconductors. These advances are enabling new levels of spectral selectivity, radiation hardness, sensitivity, and device integration, while opening opportunities across a broad range of applications. This roadmap provides a comprehensive overview of the current landscape of UV-C photodetection, spanning established and emerging material platforms (Ga2O3, AlGaN, BN, diamond, MgZnO, 2-dimensional materials, metal halide perovskites, micro-electromechanical systems), and their applications in metrology, astronomy, communications, environmental monitoring, fire detection, missile warning, gas sensing, and medical diagnostics. By identifying opportunities, bottlenecks, and future directions, this roadmap aims to support both newcomers and established researchers, with the aim of accelerating the translation of UV-C photodetectors into impactful technologies.

physics.app-ph↗

arXiv2021

Quantifying the Excitonic Static Disorder in Organic Semiconductors

Organic semiconductors are disordered molecular solids and as a result, their internal charge dynamics and ultimately, the performance of the optoelectronic devices they constitute, are governed by energetic disorder. To ascertain how energetic disorder impacts charge generation, exciton transport, charge transport, and the performance of organic semiconductor devices, an accurate approach is first required to measure this critical parameter. In this work, we show that the static disorder has no relation with the so-called Urbach energy in organic semiconductors. Instead, it can be obtained from photovoltaic external quantum efficiency spectra at wavelengths near the absorption onset. We then present a detailed methodology, alongside a computational framework, for quantifying the static energetic disorder associated with singlet excitons. Moreover, the role of optical interference in this analysis is considered to achieve a high-accuracy quantification. Finally, the excitonic static disorder was quantified in several technologically-relevant donor-acceptor blends, including high-efficiency PM6:Y6.

physics.app-ph↗

arXiv2021

A Universal Urbach Rule for Disordered Organic Semiconductors

In crystalline semiconductors, absorption onset sharpness is characterized by temperature dependent Urbach energies. These energies quantify the static, structural disorder causing localized exponential-tail states, and dynamic disorder from electron-phonon scattering. Applicability of this exponential-tail model to disordered solids has been long debated. Nonetheless, exponential fittings are routinely applied to sub-gap absorption analysis of organic semiconductors. Herein, we elucidate the sub-gap spectral line-shapes of organic semiconductors and their blends by temperature-dependent quantum efficiency measurements. We find that sub-gap absorption due to singlet excitons is universally dominated by thermal broadening at low photon energies and the associated Urbach energy equals the thermal energy, regardless of static disorder. This is consistent with absorptions obtained from a convolution of Gaussian density of excitonic states weighted by Boltzmann-like thermally activated optical transitions. A simple model is presented that explains absorption line-shapes of disordered systems, and we also provide a strategy to determine the excitonic disorder energy. Our findings elaborate the meaning of the Urbach energy in molecular solids and relate the photo-physics to static disorder, crucial for optimizing organic solar cells for which we present a new radiative open-circuit voltage limit.

physics.optics↗

arXiv2021

Direct quantification of quasi-Fermi level splitting in organic semiconductor devices

Non-radiative losses to the open-circuit voltage are a primary factor in limiting the power conversion efficiency of organic photovoltaic devices. The dominant non-radiative loss is intrinsic to the active layer and can be determined from the quasi-Fermi level splitting (QFLS) and the radiative thermodynamic limit of the photovoltage. Quantification of the QFLS in thin film devices with low mobility is challenging due to the excitonic nature of photoexcitation and additional sources of nonradiative loss associated with the device structure. This work outlines an experimental approach based on electro-modulated photoluminescence, which can be used to directly measure the intrinsic non-radiative loss to the open-circuit voltage; thereby, quantifying the QFLS. Drift-diffusion simulations are carried out to show that this method accurately predicts the QFLS in the bulk of the device regardless of device-related non-radiative losses. State-of-the-art PM6:Y6-based organic solar cells are used as a model to test the experimental approach, and the QFLS is quantified and shown to be independent of device architecture. This work provides a method to quantify the QFLS of organic solar cells under operational conditions, fully characterizing the different contributions to the non-radiative losses of the open-circuit voltage. The reported method will be useful in not only characterizing and understanding losses in organic solar cells, but also other device platforms such as light-emitting diodes and photodetectors.

physics.app-ph↗