arXiv subjects

Naveen K. Dandu

Publications and source records attributed to Naveen K. Dandu.

4 recordsLinked to original sources

arXiv2026

Atomic-Scale Mechanisms of Li-Ion Transport Mediated by Li10GeP2S12 in Composite Solid Polyethylene Oxide Electrolytes

Polymer electrolytes incorporating Li$_{10}$GeP$_{2}$S$_{12}$ (LGPS) nanoparticles show promise for solid-state lithium batteries owing to their enhanced ionic conductivity, though the governing mechanisms remain unclear. We combine molecular dynamics (MD) simulations, experimental ionic conductivity measurements, and density functional theory (DFT) calculations to elucidate the effect of LGPS loading on polyethylene oxide (PEO) structure and Li-ion transport. MD and experimental results agree up to 10\% LGPS, showing a volcano-shaped conductivity trend driven by polymer segmental dynamics and interfacial effects. Beyond 10\%, experiments reveal additional conductivity enhancement unexplained by MD, suggesting a distinct transport regime. DFT calculations indicate that Li-ion migration at the PEO|LGPS interface proceeds via vacancy-mediated hopping, with low barriers favored by S-rich interfacial sites and hindered by Ge. These findings link interfacial chemistry and microstructure to Li-ion dynamics, offering guidelines for designing high-performance composite polymer electrolytes.

cond-mat.mtrl-sci↗

arXiv2025

Interactive Multiscale Modeling to Bridge Atomic Properties and Electrochemical Performance in Li-CO$_2$ Battery Design

Li-CO$_2$ batteries are promising energy storage systems due to their high theoretical energy density and CO$_2$ fixation capability, relying on reversible Li$_2$CO$_3$/C formation during discharge/charge cycles. We present a multiscale modeling framework integrating Density Functional Theory (DFT), Ab-Initio Molecular Dynamics (AIMD), classical Molecular Dynamics (MD), and Finite Element Analysis (FEA) to investigate atomic and cell-level properties. The considered Li-CO$_2$ battery consists of a lithium metal anode, an ionic liquid electrolyte, and a carbon cloth cathode with Sb$_{0.67}$Bi$_{1.33}$Te$_3$ catalyst. DFT and AIMD determined the electrical conductivities of Sb$_{0.67}$Bi$_{1.33}$Te$_3$ and Li$_2$CO$_3$ using the Kubo-Greenwood formalism and studied the CO$_2$ reduction mechanism on the cathode catalyst. MD simulations calculated the CO$_2$ diffusion coefficient, Li$^+$ transference number, ionic conductivity, and Li$^+$ solvation structure. The FEA model, parameterized with atomistic simulations data, reproduced the available experimental voltage-capacity profile at 1 mA/cm$^2$ and revealed spatio-temporal variations in Li$_2$CO$_3$/C deposition, porosity, and CO$_2$ concentration dependence on discharge rates in the cathode. Accordingly, Li$_2$CO$_3$ can form large and thin film deposits, leading to dispersed and local porosity changes at 0.1 mA/cm$^2$ and 1 mA/cm$^2$, respectively. The capacity decreases exponentially from 81,570 mAh/g at 0.1 mA/cm$^2$ to 6,200 mAh/g at 1 mA/cm$^2$, due to pore clogging from excessive discharge product deposition that limits CO$_2$ transport to the cathode interior. Therefore, the performance of Li-CO$_2$ batteries can be improved by enhancing CO$_2$ transport, regulating Li$_2$CO$_3$ deposition, and optimizing cathode architecture.

cond-mat.mtrl-sci↗

arXiv2024

Exploring the Coexistence of Spin States in [Fe-(tpy-ph)$_2$]$^{2+}$ Complexes on Au(111) using ab initio calculations

In this work, we systematically study the electronic structure and stability of spin states of the [Fe-(tpy-ph)$_2$]$^{2+}$ molecule in both gas phase and on a Au(111) substrate using density functional theory +U (DFT+U) calculations. We find that the stability of the Fe$^{2+}$ ion's spin states is significantly influenced by the Hubbard U parameter. In the gas phase, the low-spin (LS, S=0) state is found to be energetically favorable for U(Fe) $\leq$ 3 eV, whereas the high-spin (HS, S=2) state is stabilized for U(Fe) > 3 eV. Interaction with the Au(111) substrate is found to elevate the critical U for the spin-state transition to 3.5 eV. Additionally, we perform L-edge X-ray absorption spectroscopy (XAS) calculations based on time-dependent DFT (TD-DFT) for both HS and LS states. The calculated XAS suggests that the HS state more closely aligns with the experimental observations, indicating the potential coexistence of the HS state as the initial state during the X-ray excitation process. These findings enrich our understanding of spin-state dynamics in [Fe-(tpy-ph)$_2$]$^{2+}$.

cond-mat.mtrl-sci↗

arXiv2023

Spin and electronic excitations in $4f$ atomic chains on Au(111) substrates

High spin systems, like those that incorporate rare-earth $4f$ elements (REEs), are increasingly relevant in many fields. Although research in such systems is sparse, the large Hilbert spaces they occupy are promising for many applications. In this work, we examine a one-dimensional linear array of europium (Eu) atoms on a Au(111) surface and study their electronic and magnetic excitations. Ab initio calculations using VASP with PBE+U are employed to study the structure. We find Eu atoms to have a net charge when on gold, consistent with a net magnetic momemt of $\simeq 3.5 μ_B$. Examining various spin-projection configurations, we can evaluate first and second neighbor exchange energies in an isotropic Heisenberg model between spin-$\frac{7}{2}$ moments to obtain $J_1 \approx -1.2 \, \mathrm{K}$ and $J_2 \approx 0.2 \, \mathrm{K}$ for the relaxed-chain atomic separation of $a \approx 5$ $\mathrm{\dot{A}}$. These parameters are used to obtain the full spin excitation spectrum of a physically realizable four-atom chain. The large $|J_1|/J_2$ ratio results in a highly degenerate ferromagnetic ground state that is split by a significant easy plane single ion anisotropy of $0.6$ K. Spin-flip excitations are calculated to extract differential conductance profiles as those obtained by scanning tunneling microscopy techniques. We uncover interesting behavior of local spin excitations, especially as we track their dispersion with applied magnetic fields.

cond-mat.mes-hall↗