A modified physics-informed neural network is used to predict the dynamics of optical pulses including one-soliton, two-soliton, and rogue wave based on the coupled nonlinear Schrodinger equation in birefringent fibers. At the same time, the elastic
collision process of the mixed bright-dark soliton is predicted. Compared the predicted results with the exact solution, the modified physics-informed neural network method is proven to be effective to solve the coupled nonlinear Schrodinger equation. Moreover, the dispersion coefficients and nonlinearity coefficients of the coupled nonlinear Schrodinger equation can be learned by modified physics-informed neural network. This provides a reference for us to use deep learning methods to study the dynamic characteristics of solitons in optical fibers.
Based on conservation laws as one of the important integrable properties of nonlinear physical models, we design a modified physics-informed neural network method based on the conservation law constraint. From a global perspective, this method impose
s physical constraints on the solution of nonlinear physical models by introducing the conservation law into the mean square error of the loss function to train the neural network. Using this method, we mainly study the standard nonlinear Schrodinger equation and predict various data-driven optical soliton solutions, including one-soliton, soliton molecules, two-soliton interaction, and rogue wave. In addition, based on various exact solutions, we use the modified physics-informed neural network method based on the conservation law constraint to predict the dispersion and nonlinear coefficients of the standard nonlinear Schrodinger equation. Compared with the traditional physics-informed neural network method, the modified method can significantly improve the calculation accuracy.
We use the physics-informed neural network to solve a variety of femtosecond optical soliton solutions of the high order nonlinear Schrodinger equation, including one-soliton solution, two-soliton solution, rogue wave solution, W-soliton solution and
M-soliton solution. The prediction error for one-soliton, W-soliton and M-soliton is smaller. As the prediction distance increases, the prediction error will gradually increase. The unknown physical parameters of the high order nonlinear Schrodinger equation are studied by using rogue wave solutions as data sets. The neural network is optimized from three aspects including the number of layers of the neural network, the number of neurons, and the sampling points. Compared with previous research, our error is greatly reduced. This is not a replacement for the traditional numerical method, but hopefully to open up new ideas.
Leveraging domain knowledge including fingerprints and functional groups in molecular representation learning is crucial for chemical property prediction and drug discovery. When modeling the relation between graph structure and molecular properties
implicitly, existing works can hardly capture structural or property changes and complex structure, with much smaller atom vocabulary and highly frequent atoms. In this paper, we propose the Contrastive Knowledge-aware GNN (CKGNN) for self-supervised molecular representation learning to fuse domain knowledge into molecular graph representation. We explicitly encode domain knowledge via knowledge-aware molecular encoder under the contrastive learning framework, ensuring that the generated molecular embeddings equipped with chemical domain knowledge to distinguish molecules with similar chemical formula but dissimilar functions. Extensive experiments on 8 public datasets demonstrate the effectiveness of our model with a 6% absolute improvement on average against strong competitors. Ablation study and further investigation also verify the best of both worlds: incorporation of chemical domain knowledge into self-supervised learning.
We envision that dispersion between two polymeric materials on mesoscales would create new composites with properties that are much more superior to the components alone. Here we elucidate the dispersion between two of most abundant natural polysacch
arides, starch and chitosan, which form mesoscale composites that may promise many applications. By using X-ray microscopic imaging, small-angle X-ray scattering, and differential scanning calorimetry, we were able to characterize the interactions of chitosan and starch in the mesoscale composites. The morphology of the composite is far more complex from the simple mixture of starch granules with a nominal size of a few micrometers and chitosan microbundles of tens and hundreds of micrometers. This unique morphology can only be explained by the enhanced miscibility of chitosan in a starch granular matrix. It is evidenced that there is a possible ionic interaction between the amino group in chitosan and the hydroxyl groups in starch granules. Despite the limited solubility of chitosan in water, this ionic interaction allows for the disassembly of chitosan microbundles within the starch suspension. The result is a chemically stronger and more stable granular composite formed by two biocompatible and biodegradable polysaccharide polymers. The mechanism of chitosan to disperse throughout starch granules has implications for the application of chitosan in water and other solvents.
Tissue-like materials are required in many robotic systems to improve human-machine interactions. However, the mechanical properties of living tissues are difficult to replicate. Synthetic materials are not usually capable of simultaneously displayin
g the behaviors of the cellular ensemble and the extracellular matrix. A particular challenge is identification of a cell-like synthetic component which is tightly integrated with its matrix and also responsive to external stimuli at the population level. Here, we demonstrate that cellular-scale hydrated starch granules, an underexplored component in materials science, can turn conventional hydrogels into tissue-like materials when composites are formed. Using several synchrotron-based X-ray techniques, we reveal the mechanically-induced motion and training dynamics of the starch granules in the hydrogel matrix. These dynamic behaviors enable multiple tissue-like properties such as strain-stiffening, anisotropy, mechanical heterogeneity, programmability, mechanochemistry, impact absorption, and self-healability. The starch-hydrogel composites can be processed as robotic skins that maintain these tissue-like characteristics.
