arXiv subjects

Enrique Arévalo Rodríguez

Publications and source records attributed to Enrique Arévalo Rodríguez.

3 recordsLinked to original sources

arXiv2026

The Hidden Cost of Alloying: Disorder-Driven Transport Collapse in TMDs

Alloying in two dimensional semiconductors is widely used to tune bandgaps, yet its implications for charge and energy transport remain poorly understood. Here, we investigate MoS2xSe2(1-x) alloys as a model system to study the interplay between composition, thickness, and disorder. Optical transitions and valence band dispersions evolve continuously with both stoichiometry and number of layers, with negligible bandgap bowing and a composition dependent attenuation of thickness driven renormalization. In contrast, time resolved spatial mapping of photoexcited carriers reveals a pronounced and asymmetric collapse of carrier diffusivity at intermediate compositions, which cannot be accounted for by changes in effective mass or band alignment, and instead emerges from strong real space fluctuations in the local energetic landscape generated by random chalcogen substitution. Microscopic simulations reproduce the experimental trends and show that the character of disorder depends critically on the direction of alloying, producing either scattering barriers or deep trapping sites. Together, these results demonstrate that transport in TMD alloys is governed by disorder physics, overlooked by conventional optical and photoemission probes at equilibrium. Our findings establish transport as a stringent metric of electronic quality and high-light intrinsic limitations in the usage of TMD alloys for layered semiconductor devices.

cond-mat.mtrl-sci↗

arXiv2026

Exciton Transport in Disordered Perovskite Nanocrystal Solids

Solution-processed thin films of colloidal lead halide perovskite (LHP) nanocrystals (NCs) show great potential for the implementation into optoelectronic devices such as light-emitting diodes (LEDs), lasers, and solar cells. However, these hybrid LHP NC solids exhibit non-negligible size and shape polydispersity, which introduces both structural and energetic disorder. Here, we resolve the exciton dynamics in space, time, and energy to elucidate the impact of different forms of disorder (structural and energetic) on exciton transport. We show that the disorder depends sensitively on the length of the alkylamine ligand used in the synthesis. While shorter alkyl chain lengths lead to high polydispersity, longer alkyl chains lead to more monodispersed and smaller particles where quantum confinement becomes more pronounced and, consequently, lead to increased energetic disorder. Strikingly, we find that exciton transport is less efficient in NC solids with long alkyl chain ligands, despite having a significantly more monodisperse ensemble. This demonstrates that energetic disorder, rather than structural disorder, is the dominant factor for predicting exciton transport within these materials. These findings reveal the critical role of ligand engineering in designing high-performance optoelectronic devices based on hybrid LHP NCs, providing new insights into energy transport dynamics in disordered systems and highlighting the versatility of these materials for advanced photonic and optoelectronic applications.

cond-mat.mtrl-sci↗

arXiv2025

Quantifying non-Gaussian diffusion in transient microscopy using excess kurtosis

Research on energy transport has advanced in recent years with the emergence of transient microscopy techniques that allow for imaging of carriers with high spatial and temporal resolution. In this context, transient scattering microscopy (TScM), has emerged as an alternative to traditional techniques. However, the sensitivity of TScM to different carriers can complicate the interpretation of results, highlighting the need to develop models tailored to TScM. Here, TScM is used to visualize exciton transport in bulk TMDCs. We show that exciton populations exhibit non-Gaussian profiles by analyzing the their excess kurtosis. Numerical simulations incorporating anomalous diffusion -- such as Auger recombination and trap states -- reproduce these experimental observations. Furthermore, by tuning the injected carrier density, we demonstrate that the temporal signature of the kurtosis is distinct for Auger-dominated and trap-dominated regimes. Additionally, we find that traditional Gaussian-fitting methods can yield inconsistent results for the extracted diffusivities. As an alternative, we implement a discrete variable calculation which yields robust, consistent diffusivity values. Our results establish kurtosis as a vital diagnostic parameter for identifying anomolous diffusion and demonstrate the necessity of moving beyond Gaussian approximations for accurate analysis of TScM data.

cond-mat.mtrl-sci↗