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Kaustuv Chatterjee

Publications and source records attributed to Kaustuv Chatterjee.

3 recordsLinked to original sources

Origin of bias-voltage-dependent transient negative capacitance in PZT ferroelectric capacitor with labyrinthine-like domains

We investigated how the bias-voltage-dependent variation in the ferroelectric domain switching pathways affects the transient negative capacitance in multidomain PZT ferroelectric capacitor with labyrinthine-like domains having, primarily, 90$^\circ$ walls. Using the vector piezoresponse force microscopy, x-ray photoelectron spectroscopy, and energy dispersive x-ray spectroscopy, we show that, together with strain, local variation in composition results in the formation of labyrinthine domains in epitaxial films of thickness $\sim$1 $μ$m. Clear signature of emergence of bias-voltage-dependent pathways could be observed in the Raman modes exhibiting splitting due to an intermediate state - different from the initial and final states - at the ``intermediate state of switching". The polarization relaxation patterns also show different states emerging depending on the bias voltage characteristics. The phase-field simulation of relaxation of ``intermediate state of switching" corroborates the experimental results and also exhibits dependence of the domain-wall area on the bias voltage and damping parameter. Combining the results of experiments and theoretical calculation, we show, therefore, that the variation of bias voltage leads to a change in the domain switching pathways and each pathway is associated with specific domain-wall area at the ``intermediate state of switching". Since, the net domain-wall area at the ``intermediate state of switching" governs the magnitude of transient negative capacitance, this work thus traces the origin of tunability of transient negative capacitance in PZT ferroelectric capacitor.

cond-mat.mtrl-sci↗

Observation of a Novel Charge Density Wave Superstructure in Monolayer 1T-$VS_{2}$ at Room Temperature and its Evolution in Multilayers

Spontaneous formation of charge density wave (CDW) superstructures in monolayers (MLs) of a two-dimensional (2D) crystal lattice is fundamental in understanding its complex quantum states. We report a successful top-down liquid phase exfoliation and stamp transfer process (LPESTP) to create ML VS\textsubscript{2}, undergoing a CDW transition at room temperature. Using high-resolution transmission electron microscopy (HRTEM) and electron diffraction (ED), we observed the coexistence of 1T and 2H polymorphic phases in VS\textsubscript{2} at room temperature, and only the 1T phase undergoes CDW transition. We discovered a novel incommensurate CDW superstructure ($\sqrt{7} \times \sqrt{7}$) R19.1\textsuperscript{o} in ML 1T-VS\textsubscript{2}. With an increase in the number of layers, the CDW order changes to a commensurate ($2 \times 2\times 1$) superstructure. Using angle-dependent photoelectron spectroscopy and TEM, we have shown that vanadium atoms self-intercalate as V\textsuperscript{3+} ions in multilayer VS\textsubscript{2} and are responsible for the evolution of the CDW superstructure from the incommensurate ($\sqrt{7} \times \sqrt{7}$) R 19.1\textsuperscript{o} to the commensurate ($2\times2\times1$) order. We also report the observation of novel Moiré superlattices in twisted bilayer 1T-VS\textsubscript{2} flakes with trapped CDW superstructure of the monolayer. The density functional theory (DFT) calculation performed on ML 1T-VS\textsubscript{2} show that the observed ($\sqrt{7} \times \sqrt{7}$) R 19.1\textsuperscript{o} CDW superstructure has lower energy compared to that of the pristine undistorted ML and the CDW instability is driven by formation of strong soft-phonon modes. Our findings provide an important platform for understanding the evolution of CDW superstructures in 1T-VS\textsubscript{2} with layer numbers and V self-intercalation.

cond-mat.mtrl-sci↗

Reactive Glass Metal Interaction under Ambient Conditions Enables Surface Modification of Gold Nanoislands

Stabilizing gold nanoparticles with tunable surface composition via reactive metal support interactions under ambient conditions remains a significant challenge. We discovered that a reactive glass metal interaction (RGMI) under ambient conditions, driven by the intrinsic catalytic activity of gold nanoislands (GNIs) and the unique properties of sodium aluminophosphosilicate glass, including its chemical composition, molar volume, and high Na ion mobility, enables the formation of robustly anchored GNIs with altered surface compositions. Comprehensive characterization reveals that the adsorption of Na and P at the GNI surfaces induces lattice distortions in the Au(111) planes. Additionally, a smooth GNI glass interface significantly influences the hot carrier dynamics of the GNIs. Altogether, RGMI presents a versatile strategy for engineering stable, multi element nanostructures with potential applications in heterogeneous catalysis, sensing, and optoelectronics.

cond-mat.mtrl-sci↗