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Raghvender Raghvender

Publications and source records attributed to Raghvender Raghvender.

4 recordsLinked to original sources

BattVAE-GP: Generative Modeling of Long-Horizon Battery Degradation with Uncertainty Quantification

Long-horizon physics-based simulations of battery degradation provide mechanistic insight but remain computationally expensive, limiting their use for dense exploration of operating conditions over extended cycle life. Here, we propose a hybrid physics-probabilistic learning framework for surrogate modeling of lithium-ion battery degradation trajectories at unseen charging rates. Cycle-resolved degradation data generated with a DFN/P2D electrochemical model in PyBaMM are first transformed into capacity-aligned voltage and derivative features and encoded using a Variational Autoencoder (VAE). The resulting two-dimensional latent space organizes degradation trajectories according to both cycle progression and charging protocol. A sparse multitask Gaussian process (GP) is then trained in this latent space using cycle number and C-rate as input variables, providing continuous interpolation of latent degradation dynamics together with posterior uncertainty estimates. Under protocol-level holdout evaluation, the latent-space GP accurately recovers unseen C-rate trajectories and exhibits uncertainty behavior consistent with the support of the training data. When queried at unseen interior C-rates, the model generates latent trajectories that remain coherently positioned between neighboring simulated protocols. Decoding the GP-predicted latent states through the frozen VAE decoder yields smooth voltage-capacity evolution, while Monte Carlo propagation of the GP latent posterior through an auxiliary latent to State of Health (SOH) predictor provides uncertainty-aware SOH estimates. The proposed BattVAE-GP framework therefore offers a computationally efficient and uncertainty-aware surrogate for long-horizon degradation modeling, providing a structured basis for extending battery health prediction toward richer operating conditions and future simulation-experiment fusion.

cs.LG

AI-Driven Phase Identification from X-ray Hyperspectral Imaging of cycled Na-ion Cathode Materials

Na-ion batteries have emerged as viable candidates for large-scale energy storage applica- tions due to resource abundance and cost advantages. The constraints imposed on their performance and durability, for instance, by complex phase transformations in positive electrode materials during electrochemical cycling, can be addressed and are thus not detrimental to their development. However, diffusion-limited Na-ion transport can drive spatially heterogeneous phase nucleation and propagation, leading to multiphase coexis- tence and locally non-uniform electrochemical activity, generating complex reaction path- ways that challenge both mechanistic understanding and predictive material optimization. These challenges can be addressed by investigating single-crystalline regions of materials, i.e. down to the scale of individual particles, although such analyses are often constrained by energetically and/or spatially sparse hyperspectral datasets. Here, we developed an AI-driven method to process hyperspectral data under sparse sampling conditions and generate multiphase maps with nanometer-scale resolution over a micrometer-scale field of view. We applied this processing on scanning transmission X-ray microscopy (STXM) data to determine the distribution and coexistence of phases in individual particles of NaxV2(PO4)2F3 cathode materials, at different states of charge. The methodology relies on a workflow which combines a Gaussian mixture variational autoencoder (GMVAE) algorithm with the Pearson corre- lation coefficient to identify the sodium content and map their spatial distribution. Our approach reveals nanoscale phase heterogeneity and evolution within individual particles, and improves the reliability of phase detection by identifying ambiguity zones, false assign- ments, and transition phases localized at grain boundaries.

cond-mat.mtrl-sci

Ab-initio study of structural, vibrational and non-linear optical properties of (TiO2)-(Tl2O)-(TeO2) glasses

This paper reports on a systematic first-principles molecular dynamics investigation of binary (TlO$_{0.5}$)$_{y}$-(TeO$_2$)$_{1-y}$ and ternary $(TiO$_{2}$)$_{x}$-(TlO$_{0.5}$)$_{y}$-(TeO$_2$)_{1-x-y}$ tellurite glasses. The obtained structural models are validated against available measured X-ray pair distribution functions. In the binary system, increasing TlO$_{0.5}$ content induces network depolymerization through the reduction of Te coordination number, the substitution of Te-O-Te linkages with Te=O$^{-}$...Tl$^{+}$ units, and the proliferation of non-bridging oxygens. In addition, rings analysis demonstrates a loss of the network connectivity via the opening of small n-membered rings. In contrast, TiO$_2$ acts as a network former in ternary glasses, preserving Te coordination number, and promoting a high fraction of bridging oxygens. Ti atoms induces a network repolymerization that manifests through the formation of smaller Ti-containing n-membered rings thereby balancing the strong effect of Tl$_2$O modifier. Beside the structural analysis, we also computed Raman spectra and non-linear optical properties on the obtained large periodic models. Our results reproduce experimental trends in Raman band shifts with composition, while nonlinear optical calculations show that <$\chi^{(3)}$> remains stable with TlO$_{0.5}$ addition in binary glasses, consistent with experiment. In the case of ternary systems, we find that the inclusion of a small fraction of TiO$_2$ preserves the high optical nonlinearity of the TeO$_2$ network while maintaining the overall network connectivity. These results establish a predictive framework for tailoring the atomic structure and nonlinear optical response of tellurite glasses through the controlled interplay of modifiers nature and concentration.

cond-mat.mtrl-sci

Atomic scale structure and dynamical properties of (TeO$_2$)$_{1-x}$-(Na$_2$O)$_{x}$ glasses through first-principles modeling and XRD measurements

We resort to first-principles molecular dynamics, in synergy with experiments, to study structural evolution and Na$^+$ cation diffusion inside (TeO$_2$)$_{1-x}$-(Na$_2$O)$_{x}$ (x = 0.10-0.40) glasses. Experimental and modeling results show a fair quantitative agreement in terms of total X-ray structure factors and pair distribution functions, thereby setting the ground for a comprehensive analysis of the glassy matrix evolution. We find that the structure of (TeO$_2$)$_{1-x}$-(Na$_2$O)$_{x}$ glasses deviates drastically from that of pure TeO$_2$ glass. Specifically, increasing the Na$_2$O concentration leads to a reduction of the coordination number of Te atoms, reflecting the occurrence of a structural depolymerization upon introduction of the Na$_2$O modifier oxide. The depolymerization phenomenon is ascribed to the transformation of Te-O-Te bridges into terminal Te-O non bridging oxygen atoms (NBO). Consequently, the concentration of NBO increases in these systems as the concentration of the modifier increases, accompanied by a concomitant reduction in the coordination number of Na atoms. The structure factors results show a prominent peak at 1.4 A, that becomes more and more pronounced as the Na2O concentration increases. The occurrence of this first sharp diffraction peak is attributed to the growth of Na-rich channels inside the amorphous network, acting as preferential routes for alkali-ion conduction inside the relatively stable Te-O matrix. These channels enhance the ion mobility.

cond-mat.mtrl-sci