Synthesis prediction is a key accelerator for the rapid design of advanced materials. However, determining synthesis variables such as the choice of precursor materials is challenging for inorganic materials because the sequence of reactions during heating is not well understood. In this work, we use a knowledge base of 29,900 solid-state synthesis recipes, text-mined from the scientific literature, to automatically learn which precursors to recommend for the synthesis of a novel target material. The data-driven approach learns chemical similarity of materials and refers the synthesis of a new target to precedent synthesis procedures of similar materials, mimicking human synthesis design. When proposing five precursor sets for each of 2,654 unseen test target materials, the recommendation strategy achieves a success rate of at least 82%. Our approach captures decades of heuristic synthesis data in a mathematical form, making it accessible for use in recommendation engines and autonomous laboratories.

As a widely recognized approach to deep generative modeling, Variational Auto-Encoders (VAEs) still face challenges with the quality of generated images, often presenting noticeable blurriness. This issue stems from the unrealistic assumption that approximates the conditional data distribution, $p(\textbf{x} | \textbf{z})$, as an isotropic Gaussian. In this paper, we propose a novel solution to address these issues. We illustrate how one can extract a latent space from a pre-existing diffusion model by optimizing an encoder to maximize the marginal data log-likelihood. Furthermore, we demonstrate that a decoder can be analytically derived post encoder-training, employing the Bayes rule for scores. This leads to a VAE-esque deep latent variable model, which discards the need for Gaussian assumptions on $p(\textbf{x} | \textbf{z})$ or the training of a separate decoder network. Our method, which capitalizes on the strengths of pre-trained diffusion models and equips them with latent spaces, results in a significant enhancement to the performance of VAEs.

The accurate but fast calculation of molecular excited states is still a very challenging topic. For many applications, detailed knowledge of the energy funnel in larger molecular aggregates is of key importance requiring highly accurate excited state energies. To this end, machine learning techniques can be an extremely useful tool though the cost of generating highly accurate training datasets still remains a severe challenge. To overcome this hurdle, this work proposes the use of multi-fidelity machine learning where very little training data from high accuracies is combined with cheaper and less accurate data to achieve the accuracy of the costlier level. In the present study, the approach is employed to predict the first excited state energies for three molecules of increasing size, namely, benzene, naphthalene, and anthracene. The energies are trained and tested for conformations stemming from classical molecular dynamics simulations and from real-time density functional tight-binding calculations. It can be shown that the multi-fidelity machine learning model can achieve the same accuracy as a machine learning model built only on high cost training data while having a much lower computational effort to generate the data. The numerical gain observed in these benchmark test calculations was over a factor of 30 but certainly can be much higher for high accuracy data.

The recent advances in neural language models have also been successfully applied to the field of chemistry, offering generative solutions for classical problems in molecular design and synthesis planning. These new methods have the potential to fuel a new era of data-driven automation in scientific discovery. However, specialized models are still typically required for each task, leading to the need for problem-specific fine-tuning and neglecting task interrelations. The main obstacle in this field is the lack of a unified representation between natural language and chemical representations, complicating and limiting human-machine interaction. Here, we propose the first multi-domain, multi-task language model that can solve a wide range of tasks in both the chemical and natural language domains. Our model can handle chemical and natural language concurrently, without requiring expensive pre-training on single domains or task-specific models. Interestingly, sharing weights across domains remarkably improves our model when benchmarked against state-of-the-art baselines on single-domain and cross-domain tasks. In particular, sharing information across domains and tasks gives rise to large improvements in cross-domain tasks, the magnitude of which increase with scale, as measured by more than a dozen of relevant metrics. Our work suggests that such models can robustly and efficiently accelerate discovery in physical sciences by superseding problem-specific fine-tuning and enhancing human-model interactions.

We introduce Graph-Induced Sum-Product Networks (GSPNs), a new probabilistic framework for graph representation learning that can tractably answer probabilistic queries. Inspired by the computational trees induced by vertices in the context of message-passing neural networks, we build hierarchies of sum-product networks (SPNs) where the parameters of a parent SPN are learnable transformations of the a-posterior mixing probabilities of its children's sum units. Due to weight sharing and the tree-shaped computation graphs of GSPNs, we obtain the efficiency and efficacy of deep graph networks with the additional advantages of a purely probabilistic model. We show the model's competitiveness on scarce supervision scenarios, handling missing data, and graph classification in comparison to popular neural models. We complement the experiments with qualitative analyses on hyper-parameters and the model's ability to answer probabilistic queries.

The ATLAS experiment measures the properties of particles that are products of proton-proton collisions at the LHC. The ATLAS detector will undergo a major upgrade before the high luminosity phase of the LHC. The ATLAS liquid argon calorimeter measures the energy of particles interacting electromagnetically in the detector. The readout electronics of this calorimeter will be replaced during the aforementioned ATLAS upgrade. The new electronic boards will be based on state-of-the-art field-programmable gate arrays (FPGA) from Intel allowing the implementation of neural networks embedded in firmware. Neural networks have been shown to outperform the current optimal filtering algorithms used to compute the energy deposited in the calorimeter. This article presents the implementation of a recurrent neural network (RNN) allowing the reconstruction of the energy deposited in the calorimeter on Stratix 10 FPGAs. The implementation in high level synthesis (HLS) language allowed fast prototyping but fell short of meeting the stringent requirements in terms of resource usage and latency. Further optimisations in Very High-Speed Integrated Circuit Hardware Description Language (VHDL) allowed fulfilment of the requirements of processing 384 channels per FPGA with a latency smaller than 125 ns.

The physics potential of massive liquid argon TPCs in the low-energy regime is still to be fully reaped because few-hits events encode information that can hardly be exploited by conventional classification algorithms. Machine learning (ML) techniques give their best in these types of classification problems. In this paper, we evaluate their performance against conventional (deterministic) algorithms. We demonstrate that both Convolutional Neural Networks (CNN) and Transformer-Encoder methods outperform deterministic algorithms in one of the most challenging classification problems of low-energy physics (single- versus double-beta events). We discuss the advantages and pitfalls of Transformer-Encoder methods versus CNN and employ these methods to optimize the detector parameters, with an emphasis on the DUNE Phase II detectors ("Module of Opportunity").

Emerging technologies like hypersonic aircraft, space exploration vehicles, and batteries avail fluid circulation in embedded microvasculatures for efficient thermal regulation. Modeling is vital during these engineered systems' design and operational phases. However, many challenges exist in developing a modeling framework. What is lacking is an accurate framework that (i) captures sharp jumps in the thermal flux across complex vasculature layouts, (ii) deals with oblique derivatives (involving tangential and normal components), (iii) handles nonlinearity because of radiative heat transfer, (iv) provides a high-speed forecast for real-time monitoring, and (v) facilitates robust inverse modeling. This paper addresses these challenges by availing the power of physics-informed neural networks (PINNs). We develop a fast, reliable, and accurate Scientific Machine Learning (SciML) framework for vascular-based thermal regulation -- called CoolPINNs: a PINNs-based modeling framework for active cooling. The proposed mesh-less framework elegantly overcomes all the mentioned challenges. The significance of the reported research is multi-fold. First, the framework is valuable for real-time monitoring of thermal regulatory systems because of rapid forecasting. Second, researchers can address complex thermoregulation designs inasmuch as the approach is mesh-less. Finally, the framework facilitates systematic parameter identification and inverse modeling studies, perhaps the current framework's most significant utility.

In this work, we propose a deep learning (DL)-based constitutive model for investigating the cyclic viscoelastic-viscoplastic-damage behavior of nanoparticle/epoxy nanocomposites with moisture content. For this, a long short-term memory network is trained using a combined framework of a sampling technique and a perturbation method. The training framework, along with the training data generated by an experimentally validated viscoelastic-viscoplastic model, enables the DL model to accurately capture the rate-dependent stress-strain relationship and consistent tangent moduli. In addition, the DL-based constitutive model is implemented into finite element analysis. Finite element simulations are performed to study the effect of load rate and moisture content on the force-displacement response of nanoparticle/ epoxy samples. Numerical examples show that the computational efficiency of the DL model depends on the loading condition and is significantly higher than the conventional constitutive model. Furthermore, comparing numerical results and experimental data demonstrates good agreement with different nanoparticle and moisture contents.

Optimizing energy consumption and coordination of utility systems have long been a concern of the building industry. Buildings are one of the largest energy consumers in the world, making their energy efficiency crucial for preventing waste and reducing costs. Additionally, buildings generate substantial amounts of raw data, which can be used to understand energy consumption patterns and assist in developing optimization strategies. Using a real-world dataset, this research aims to identify the factors that influence building cost reduction and energy consumption. To achieve this, we utilize three regression models (Lasso Regression, Decision Tree, and Random Forest) to predict primary fuel usage, electrical energy consumption, and cost savings in buildings. An analysis of the factors influencing energy consumption and cost reduction is conducted, and the decision tree algorithm is optimized using metaheuristics. By employing metaheuristic techniques, we fine-tune the decision tree algorithm's parameters and improve its accuracy. Finally, we review the most practical features of potential and nonpotential buildings that can reduce primary fuel usage, electrical energy consumption, and costs