arXiv subjects

Aditi Sahoo

Publications and source records attributed to Aditi Sahoo.

5 recordsLinked to original sources

arXiv2026

Operando Raman probing of mode selective electron phonon coupling in two dimensional halide perovskites

Electron phonon coupling governs charge transport, carrier relaxation, and polaron formation in halide perovskites, yet its microscopic origin in low dimensional systems remains poorly understood. Here, we combine operando, bias dependent Raman spectroscopy with density functional theory (DFT) calculations to directly probe carrier lattice interactions in two-dimensional Ruddlesden Popper perovskites,(PEA)$_2$PbI$_4$ and its fluorinated analogue, (PEA-F)$_2$PbI$_4$. Under applied electric fields, both systems exhibit mode-selective Raman linewidth broadening predominantly near 100 cm$^{-1}$, whereas other phonon modes remain largely unaffected, revealing highly selective coupling between injected carriers and specific lattice vibrations. DFT calculations identify these modes as hybrid organic inorganic vibrations involving coupled motion of the organic spacer and symmetric Pb I equatorial stretching, rather than purely inorganic phonons. Fluorination fundamentally reconstructs the vibrational landscape by modifying molecular packing, crystal symmetry, and organic inorganic coupling, resulting in changes to the phonon density of states, longer phonon lifetimes, and an enhanced carrier mediated lattice response. Notably, electrical bias produces opposite phonon lifetime evolution in thin films and single crystals: the phonon lifetime decreases by approximately 17 to 22% in thin films but increases 20 to 26% in single crystals. These contrasting responses demonstrate that structural order plays a fundamental role in determining carrier phonon interactions and phonon relaxation pathways in two-dimensional halide perovskites.

cond-mat.mtrl-sci↗

arXiv2022

Room-temperature surface multiferroicity in Y$_2$NiMnO$_6$ nanorods

We report observation of surface-defect-induced room temperature multiferroicity - surface ferromagnetism ($M_S$ at 50 kOe $\sim$0.005 emu/g), ferroelectricity ($P_R$ $\sim$2 nC/cm$^2$), and significantly large magnetoelectric coupling (decrease in $P_R$ by $\sim$80\% under $\sim$15 kOe field) - in nanorods (diameter $\sim$100 nm) of double perovskite Y$_2$NiMnO$_6$ compound. In bulk form, this system exhibits multiferroicity only below its magnetic transition temperature $T_N$ $\approx$ 70 K. On the other hand, the oxygen vacancies, formed at the surface region (thickness $\sim$10 nm) of the nanorods, yield long-range magnetic order as well as ferroelectricity via Dzyloshinskii-Moriya exchange coupling interactions with strong Rashba spin-orbit coupling. Sharp drop in $P_R$ under magnetic field indicates strong cross-coupling between magnetism and ferroelectricity as well. Observation of room temperature magnetoelectric coupling in nanoscale for a compound which, in bulk form, exhibits multiferroicity only below 70 K underscores an alternative pathway for inducing magnetoelectric multiferroicity via surface defects and, thus, in line with magnetoelectric property observed, for example, in domain walls or boundaries or interfaces of heteroepitaxially grown thin films which do not exhibit such features in their bulk.

cond-mat.mtrl-sci↗

arXiv2021

Electric-field-driven resistive transition in multiferroic SrCo$_2$Fe$_{16}$O$_{27}$/Sr$_3$Co$_2$Fe$_{24}$O$_{41}$composite

We report observation of electric-field-driven resistive transition at a characteristic threshold field $E_{th}(T)$ across a temperature range 10-200 K in an off-stoichiometric composite of (~80 vol%) W- and (~20 vol%) Z-type hexaferrites. The dielectric constant $ε$ and the relaxation time constant $τ$ too exhibit anomalous jump at $E_{th}(T)$. The $E_{th}(T)$, the extent of jump in resistivity ($Δρ$), and the hysteresis associated with the jump [$ΔE_{th}(T)$] are found to decrease systematically with the increase in temperature ($T$). Several temperature-driven phase transitions have also been noticed in low and high resistive states (LRS and HRS). The temperature-driven conduction turns out to be governed by activated hopping of small polarons at all the phases with electric ($E$) and magnetic ($H$) field dependent activation energy $U(E,H)$. Interestingly, as the temperature is raised, the $E$-driven conduction at a fixed temperature evolves from $\textit{Ohmic}$ to $\textit{non-Ohmic}$ across 10-200 K and within 110-200 K, $ρ$ follows three-dimensional variable range hopping (3D-VRH) with stretched exponential $\sim$ $exp[(E_0/E)^4]$ or power law $\sim$ $(E_0/E)^m$ ($m$ varies within $\sim$0.6-0.7 and $\sim$0.6-0.8 at LRS and HRS, respectively) dependence depending on the localization length ($ζ_E$) to diffusion length ($d_E$) ratio associated with $E$-driven conduction. The $ρ(E,T)$ follows universal scaling only at LRS within 10-110 K but not at higher temperature or at HRS. The entire set of observations has been discussed within the framework of structural evolution of the point-defect (cation vacancies or oxygen excess) network. This comprehensive map of esoteric $ρ-E-T-H$ and $ε-E-T-H$ patterns provides insights on defect driven effects in a composite useful for tuning both the resistive transition and multiferroicity.

cond-mat.str-el↗

arXiv2020

Large structure-dependent room temperature exchange bias in self-assembled BiFeO3 nanoparticles

We studied the magnetic properties of self-assembled aggregates of BiFeO3 nanoparticles (~ 20-40 nm). The aggregates formed two different structures - one with limited and another with massive cross-linking - via `drying-mediated self-assembly' process following dispersion of the nanoparticles within different organic solvents. They exhibit large coercivity H_C (>1000 Oe) and exchange bias field H_E (~ 350-900 Oe) in comparison to what is observed in isolated nanoparticles (H_C ~ 250 Oe; H_E ~ 0). The H_E turns out to be switching from negative to positive depending on the structure of the aggregates with |H_E| being larger. The magnetic force microscopy reveals the magnetic domains (extending across 7-10 nanoparticles) as well as the domain switching characteristics and corroborate the results of magnetic measurements. Numerical simulation of the `drying-mediated-self-assembly' process shows that the nanoparticle-solvent interaction plays an important role in forming the `nanoparticle aggregate structures' observed experimentally. Numerical simulation of the magnetic hysteresis loops, on the other hand, points out the importance of spin pinning at the surface of nanoparticles as a result of surface functionalization of the particles in different suspension media. Depending on the concentration of pinned spins at the surface pointing preferably along the easy-axis direction - from greater than 50\% to less than 50% - H_E switches from negative to positive. Quite aside from bulk sample and isolated nanoparticle, nanoparticle aggregates - resulting from surface functionalization - therefore, offer remarkable tunability of properties depending on structures.

cond-mat.mes-hall↗

arXiv2019

Effect of surface pinning on magnetic nanostuctures

Magnetic nanostructures are often considered as highly functional materials because they exhibit unusual magnetic properties under different external conditions. We study the effect of surface pinning on the core-shell magnetic nanostuctures of different shapes and sizes considering the spin-interaction to be Ising-like. We explore the hysteresis properties and find that the exchange bias, even under zero field cooled conditions, increases with increase of, the pinning density and the fraction of up-spins among the pinned ones. We explain these behavior analytically by introducing a simple model of the surface. The asymmetry in hysteresis is found to be more prominent in a inverse core-shell structure, where spin interaction in the core is antiferromagnetic and that in the shell is ferromagnetic. These studied of inverse core-shell structure are extended to different shapes, sizes, and different spin interactions, namely Ising, XY- and Heisenberg models in three dimension. We also briefly discuss the pinning effects on magnetic heterostructures.

cond-mat.mes-hall↗