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Mohammad Taha

Publications and source records attributed to Mohammad Taha.

3 recordsLinked to original sources

AutoRASOR: Autonomous Rapid Scanning Electron Microscope Operator

Scanning Electron Microscopy (SEM) is a foundational technique for characterizing material microstructure, which dictates many fundamental physical and chemical properties. With the rise of Self-Driving Labs (SDLs), samples are now synthesized in large batches, demanding equally high-throughput, autonomous characterization. Existing automated electron microscopy pipelines are task-specific: they detect pre-defined features, optimize known properties, or require prior knowledge of the sample, restricting each pipeline to the material system it was built for. We introduce AutoRASOR, a task-agnostic autonomous SEM pipeline that captures the multi-scale morphology of an unknown sample without domain-specific pre-training, fine-tuning, or human prompting. AutoRASOR embeds micrographs in real time with a vision foundation model (VFM), DINOv3, and selects regions of interest (ROIs) through two complementary policies: Latent Farthest Point Sampling (LFPS) and active learning on morphological ambiguity, which is the conditional variance of unresolved fine-scale features given lower magnification appearance. Active learning on ambiguity consistently captures more diverse and rare morphologies than random ROI selection, while LFPS reliably recovers the specimen's morphological distribution within a limited capture budget, tested both on real SEM micrographs and synthetic phase-field images. By shifting autonomous characterization from pre-defined, task-specific targeting of features to morphological survey, AutoRASOR generates information-rich multi-scale datasets for diverse downstream tasks. Without the need for domain-specific pre-training or prior material assumptions, this framework can be deployed out-of-the-box to characterize novel materials produced by SDLs.

eess.IV↗

Hopping of nanoparticles in optical tweezers governed by Mie resonances

Optical tweezers have become a standard tool for manipulating microscale and nanoscale particles and probing their local environments. However, complex particle dynamics under optical forces typically require structured light fields, multi-beam traps, or engineered environments. Here we achieve complex particle dynamics in a single Gaussian-beam optical tweezer. The effect originates from higher-order Mie resonances supported by wavelength-scale particles. In our optical tweezer, small particles in the regime of Rayleigh scattering or the lowest-order dipole-type Mie modes remain confined at the beam center. By contrast, particles within the range of sizes corresponding to quadrupole-type Mie modes exhibit more complex behavior. In a linearly polarized Gaussian beam, these particles are trapped in a potential with two off-axis equilibria. We observe thermally driven hopping between these equilibria, with the hopping frequency controlled by the laser power. In a circularly polarized Gaussian beam, the particles are confined to a stable orbit and exhibit circular motion driven by the spin (circular-polarization) degree of freedom of the beam, with angular velocity dependent on the laser power. These results reveal higher-order Mie resonances as an intrinsic mechanism behind complex optical forces. This establishes Mie-resonant nanophotonics as a flexible platform for inducing and controlling complex motion in optical tweezers for nanoparticle manipulation as well as sensing of local environments.

physics.optics↗

Switchable optical trapping of Mie-resonant phase-change nanoparticles

Optical tweezers revolutionized the manipulation of nanoscale objects. Typically, tunable manipulations of optical tweezers rely on adjusting either the trapping laser beams or the optical environment surrounding the nanoparticles. We present a novel approach to achieve tunable and switchable trapping using nanoparticles made of a phase-change material (vanadium dioxide or VO$_2$). By varying the intensity of the trapping beam, we induce transitions of the VO$_2$ between monoclinic and rutile phases. Depending on the nanoparticles' sizes, they exhibit one of three behaviours: small nanoparticles (in our settings, radius $<0.12$ wavelength $λ$) remain always attracted by the laser beam in both material phases, large nanoparticles ($>0.22 λ$) remain always repelled. However, within the size range of $0.12$-$0.22 λ$, the phase transition of the VO$_2$ switches optical forces between attractive and repulsive, thereby pulling/pushing them towards/away from the beam centre. The effect is reversible, allowing the same particle to be attracted and repelled repeatedly. The phenomenon is governed by Mie resonances supported by the nanoparticle and their alterations during the phase transition of the VO$_2$. This work provides an alternative solution for dynamic optical tweezers and paves a way to new possibilities, including optical sorting, light-driven optomechanics and single-molecule biophysics.

physics.optics↗