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Atomically thin two-dimensional (2D) materials exhibit extraordinary optical, electrical, and mechanical properties. Many functional nanostructures and devices of exceptional performance based on 2D materials have been demonstrated. However, the processing of 2D materials remains challenging due to inadequacies that are mainly driven by high fabrication cost, complex steps, and inefficient impurity control. On the other hand, laser-aided processing techniques offer versatility, nanoscale precision, and high throughput. Numerous efforts have showcased the implementation of laser processing and functionalization of 2D materials to control their physical properties and optimize device functionality. In this Perspective, we summarize research progress on laser-enabled thinning, patterning, doping, and functionalization of 2D materials. Continuing advances in optical processing techniques are anticipated to further accelerate the deployment of 2D materials and devices in many fields, including photonics, optoelectronics, and sensor applications. 

Since Multiphoton Lithography (MPL) is applied as an additive manufacturing technique for the fabrication of operational microsystems, the need to predict the mechanical response of the fabricated structures emerges. This work focuses on determining the Young's Modulus of structures fabricated via MPL. With this objective in mind, two series of experiments were designed and conducted: the first one for the determination of the factors whose impact is significant, and the second one for generating a dataset used in the training of a machine learning tool that will define the suitable set of fabrication parameters for the fabrication of a structure with desired Young's Modulus. 

Abstract The electronic and optical properties of 2D transition metal dichalcogenides are dominated by strong excitonic resonances. Exciton dynamics plays a critical role in the functionality and performance of many miniaturized 2D optoelectronic devices; however, the measurement of nanoscale excitonic behaviors remains challenging. Here, a near‐field transient nanoscopy is reported to probe exciton dynamics beyond the diffraction limit. Exciton recombination and exciton–exciton annihilation processes in monolayer and bilayer MoS₂are studied as the proof‐of‐concept demonstration. Moreover, with the capability to access local sites, intriguing exciton dynamics near the monolayer‐bilayer interface and at the MoS₂nano‐wrinkles are resolved. Such nanoscale resolution highlights the potential of this transient nanoscopy for fundamental investigation of exciton physics and further optimization of functional devices. 

Biomimetic and Bioinspired designs have been investigated due to the advances in modeling, mechanics and experimental characterization of structural features of living organisms. To accomplish bioinspiration for fields such as robotics, adhesives and smart materials, it is required to comprehend how Nature accomplished enhanced mechanical behavior. Among the plethora of complex organisms spanning at different lengthscales, the deep sea sponge Euplectella Aspergillum has been of particular interest due to its lattice structure that can be the framework to design mechanical metamaterials. However, despite its intriguing morphology, constraints in the fabrication and modeling of scalable and nonuniform materials has hindered the study of its mechanical performance and how to harness it. Moreover, a comprehensive FEA model that encompasses the whole spectrum of its constitutive and structural performance has not been reported. In this study, it is aimed to characterize and model the mechanical behavior of this sponge from a structural standpoint. Utilizing various experimental techniques, an FEA mechanical model is developed to study the nonlinear buckling analysis of the sponge’s lattice structure and its resilience to failure. Finally, through topology optimization and sensitivity analysis, a new mechanical metamaterial is proposed. Our results elucidate how mechanical characterization and FEA modeling can be employed for a deeper understanding of Nature’s tailored hierarchy and the design of metamaterials. 

C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials. 

C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials. 

Abstract Recent advancements in manufacturing, finite element analysis (FEA), and optimization techniques have expanded the design possibilities for metamaterials, including isotropic and auxetic structures, known for applications like energy absorption due to their unique deformation mechanism and consistent behavior under varying loads. However, achieving simultaneous control of multiple properties, such as optimal isotropic and auxetic characteristics, remains challenging. This paper introduces a systematic design approach that combines modeling, FEA, genetic algorithm, and optimization to create tailored mechanical behavior in metamaterials. Through strategically arranging 8 distinct neither isotropic nor auxetic unit cell states, the stiffness tensor in a 5 × 5 × 5 cubic symmetric lattice structure is controlled. Employing the NSGA-II genetic algorithm and automated modeling, we yield metamaterial lattice structures possessing both desired isotropic and auxetic properties. Multiphoton lithography fabrication and experimental characterization of the optimized metamaterial highlights a practical real-world use and confirms the close correlation between theoretical and experimental data. 

We demonstrate the laser mediated atomic layer etching (ALEt) of silicon. Using a nanosecond pulsed 266 nm laser focused loosely over and in a parallel configuration to the surface of the silicon, we dissociate Cl2 gas to induce chlorination. Then, we use pulsed picosecond irradiation to remove the chlorinated layer. Subsequently, we perform continuous wave (CW) laser annealing to eliminate amorphization caused by the picosecond laser etching. Based on atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS), we observed strong evidence of chlorination and digital etching at 0.85 nm etching per cycle with good uniformity.