Laboratory Automation (LA) has the potential to accelerate solid-state materials discovery by enabling continuous robotic operation without human intervention. While robotic systems have been developed for tasks such as powder grinding and X-ray diffraction (XRD) analysis, fully automating powder handling at the milligram scale remains a significant challenge due to the complex flow dynamics of powders and the diversity of laboratory tasks. To address this challenge, this study proposes a novel, funnel-shaped, flexible robotic hand that preserves the softness and conical sheet designs in prior work while incorporating a controllable valve at the cone apex to enable precise, incremental dispensing of milligram-scale powder quantities. The hand is integrated with an external balance through a feedback control system based on a model of powder flow and online parameter identification. Experimental evaluations with glass beads, monosodium glutamate, and titanium dioxide demonstrated that 80% of the trials achieved an error within 2 mg, and the maximum error observed was approximately 20 mg across a target range of 20 mg to 3 g. In addition, by incorporating flow prediction models commonly used for hoppers and performing online parameter identification, the system is able to adapt to variations in powder dynamics. Compared to direct PID control, the proposed model-based control significantly improved both accuracy and convergence speed. These results highlight the potential of the proposed system to enable efficient and flexible powder weighing, with scalability toward larger quantities and applicability to a broad range of laboratory automation tasks.

We propose an extended neural adjoint (ENA) framework, which meets six key criteria for artificial intelligence-assisted inverse design of optical multilayer thin films (OMTs): accuracy, efficiency, diversity, scalability, flexibility, and interpretability. To enhance the scalability of the existing neural adjoint method, we present a novel forward neural network architecture for OMTs and introduce a material loss function into the existing neural adjoint loss function, facilitating the exploration of material configurations of OMTs. Furthermore, we present the detailed formulation of the regression activation mapping for the presented forward neural network architecture (F-RAM), a feature visualization method aimed at improving interpretability. We validated the efficacy of the material loss by conducting an ablation study, where each component of the loss function is systematically removed and evaluated. The results indicated that the inclusion of the material loss significantly improves accuracy and diversity. To substantiate the performance of the ENA-based inverse design, we compared it against the residual network-based global optimization network (Res-GLOnet). The ENA yielded the OMT solutions of an inverse design with higher accuracy and better diversity compared to the Res-GLOnet. To demonstrate the interpretability, we applied F-RAM to diverse OMT structures with similar optical properties, obtained by the proposed ENA method. We showed that distributions of feature importance for various OMT structures exhibiting analogous optical properties are consistent, despite variations in material configurations, layer number, and thicknesses. Furthermore, we demonstrate the flexibility of the ENA method by restricting the initial layer of OMTs to SiO2 and 100 nm.

Nanomaterial research is becoming a vital area for energy, medicine, and materials science, and accurate analysis of the nanoparticle topology is essential to determine their properties. Unfortunately, the lack of high-quality annotated datasets drastically hinders the creation of strong segmentation models for nanoscale imaging. To alleviate this problem, we introduce F-ANcGAN, an attention-enhanced cycle consistent generative adversarial system that can be trained using a limited number of data samples and generates realistic scanning electron microscopy (SEM) images directly from segmentation maps. Our model uses a Style U-Net generator and a U-Net segmentation network equipped with self-attention to capture structural relationships and applies augmentation methods to increase the variety of the dataset. The architecture reached a raw FID score of 17.65 for TiO$_2$ dataset generation, with a further reduction in FID score to nearly 10.39 by using efficient post-processing techniques. By facilitating scalable high-fidelity synthetic dataset generation, our approach can improve the effectiveness of downstream segmentation task training, overcoming severe data shortage issues in nanoparticle analysis, thus extending its applications to resource-limited fields.

Nanomaterials exhibit distinctive properties governed by parameters such as size, shape, and surface characteristics, which critically influence their applications and interactions across technological, biological, and environmental contexts. Accurate quantification and understanding of these materials are essential for advancing research and innovation. In this regard, deep learning segmentation networks have emerged as powerful tools that enable automated insights and replace subjective methods with precise quantitative analysis. However, their efficacy depends on representative annotated datasets, which are challenging to obtain due to the costly imaging of nanoparticles and the labor-intensive nature of manual annotations. To overcome these limitations, we introduce DiffRenderGAN, a novel generative model designed to produce annotated synthetic data. By integrating a differentiable renderer into a Generative Adversarial Network (GAN) framework, DiffRenderGAN optimizes textural rendering parameters to generate realistic, annotated nanoparticle images from non-annotated real microscopy images. This approach reduces the need for manual intervention and enhances segmentation performance compared to existing synthetic data methods by generating diverse and realistic data. Tested on multiple ion and electron microscopy cases, including titanium dioxide (TiO$_2$), silicon dioxide (SiO$_2$)), and silver nanowires (AgNW), DiffRenderGAN bridges the gap between synthetic and real data, advancing the quantification and understanding of complex nanomaterial systems.

In this paper, we address the task of characterizing the chemical composition of planetary surfaces using convolutional neural networks (CNNs). Specifically, we seek to predict the multi-oxide weights of rock samples based on spectroscopic data collected under Martian conditions. We frame this problem as a multi-target regression task and propose a novel regularization method based on f-divergence. The f-divergence regularization is designed to constrain the distributional discrepancy between predictions and noisy targets. This regularizer serves a dual purpose: on the one hand, it mitigates overfitting by enforcing a constraint on the distributional difference between predictions and noisy targets. On the other hand, it acts as an auxiliary loss function, penalizing the neural network when the divergence between the predicted and target distributions becomes too large. To enable backpropagation during neural network training, we develop a differentiable f-divergence and incorporate it into the f-divergence regularization, making the network training feasible. We conduct experiments using spectra collected in a Mars-like environment by the remote-sensing instruments aboard the Curiosity and Perseverance rovers. Experimental results on multi-oxide weight prediction demonstrate that the proposed $f$-divergence regularization performs better than or comparable to standard regularization methods including $L_1$, $L_2$, and dropout. Notably, combining the $f$-divergence regularization with these standard regularization further enhances performance, outperforming each regularization method used independently.

Accurate modeling of long-range forces is critical in atomistic simulations, as they play a central role in determining the properties of materials and chemical systems. However, standard machine learning interatomic potentials (MLIPs) often rely on short-range approximations, limiting their applicability to systems with significant electrostatics and dispersion forces. We recently introduced the Latent Ewald Summation (LES) method, which captures long-range electrostatics without explicitly learning atomic charges or charge equilibration. Extending LES, we incorporate the ability to learn physical partial charges, encode charge states, and the option to impose charge neutrality constraints. We benchmark LES on diverse and challenging systems, including charged molecules, ionic liquid, electrolyte solution, polar dipeptides, surface adsorption, electrolyte/solid interfaces, and solid-solid interfaces. Our results show that LES can effectively infer physical partial charges, dipole and quadrupole moments, as well as achieve better accuracy compared to methods that explicitly learn charges. LES thus provides an efficient, interpretable, and generalizable MLIP framework for simulating complex systems with intricate charge transfer and long-range

Understanding material surfaces and interfaces is vital in applications like catalysis or electronics. By combining energies from electronic structure with statistical mechanics, ab initio simulations can in principle predict the structure of material surfaces as a function of thermodynamic variables. However, accurate energy simulations are prohibitive when coupled to the vast phase space that must be statistically sampled. Here, we present a bi-faceted computational loop to predict surface phase diagrams of multi-component materials that accelerates both the energy scoring and statistical sampling methods. Fast, scalable, and data-efficient machine learning interatomic potentials are trained on high-throughput density-functional theory calculations through closed-loop active learning. Markov-chain Monte Carlo sampling in the semi-grand canonical ensemble is enabled by using virtual surface sites. The predicted surfaces for GaN(0001), Si(111), and SrTiO3(001) are in agreement with past work and suggest that the proposed strategy can model complex material surfaces and discover previously unreported surface terminations.

Nanophotonic structures have versatile applications including solar cells, anti-reflective coatings, electromagnetic interference shielding, optical filters, and light emitting diodes. To design and understand these nanophotonic structures, electrodynamic simulations are essential. These simulations enable us to model electromagnetic fields over time and calculate optical properties. In this work, we introduce frameworks and benchmarks to evaluate nanophotonic structures in the context of parametric structure design problems. The benchmarks are instrumental in assessing the performance of optimization algorithms and identifying an optimal structure based on target optical properties. Moreover, we explore the impact of varying grid sizes in electrodynamic simulations, shedding light on how evaluation fidelity can be strategically leveraged in enhancing structure designs.