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Kumar, Amit

Publications and source records attributed to Kumar, Amit.

At least 73 records · Page 4

Investigation of dielectric relaxation, Jahn-Teller distortion, and magnetic ordering in Y substituted Pr{sub 1−x}Y{sub x}MnO{sub 3} (0.1 ≤ x ≤ 0.4)

We report structural, magnetic, and dielectric properties of the perovskite compound Pr{sub 1−x}Y{sub x}MnO{sub 3} (0.1 ≤ x ≤ 0.4) studied using dc magnetization, ac susceptibility, neutron powder diffraction, and dielectric techniques. These compounds crystallize in orthorhombic space group (Pnma) in the temperature range 5–300 K. The Mn-O-Mn bond angle decreases with the Y substitution along with an increase in the Jahn-Teller distortion. The Jahn-Teller distortion for Pr{sub 0.9}Y{sub 0.1}MnO{sub 3} shows an anomalous change near 50 K, below which it falls sharply. Neutron powder diffraction patterns of all reported compositions at low temperature constitute additional magnetic Bragg peaks that suggest magnetic ordering. Magnetic reflections were indexed in the nuclear lattice with the propagation vector k = (0, 0, 0). Rietveld refinement of powder patterns conform to A type antiferromagnetic ordering where moments are aligned ferromagnetically in a–c plane and coupled nearly antiferromagnetically along b-axis resulting in a net ferromagnetic component along the b-direction. The antiferromagnetic transition temperature was deduced from dc magnetization and ac susceptibility data. The transition temperature decreases by nearly 22 K (from 81 K to 59 K) as yttrium content (x) increases from 0.1 to 0.4. Measurements reveal strong frequency dispersion in dielectric constant and dielectric loss. Activation energy and relaxation time are estimated from the Arrhenius plot. It is further shown that relaxation behaviour is altered with yttrium doping concentration.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Spatially-resolved mapping of history-dependent coupled electrochemical and electronical behaviors of electroresistive NiO

Bias-induced oxygen ion dynamics underpins a broad spectrum of electroresistive and memristive phenomena in oxide materials. Although widely studied by device-level and local voltage-current spectroscopies, the relationship between electroresistive phenomena, local electrochemical behaviors, and microstructures remains elusive. Here, the interplay between history-dependent electronic transport and electrochemical phenomena in a NiO single crystalline thin film with a number of well-defined defect types is explored on the nanometer scale using an atomic force microscopy-based technique. A variety of electrochemically-active regions were observed and spatially resolved relationship between the electronic and electrochemical phenomena was revealed. The regions with pronounced electroresistive activity were further correlated with defects identified by scanning transmission electron microscopy. Using fully coupled mechanical-electrochemical modeling, we illustrate that the spatial distribution of strain plays an important role in electrochemical and electroresistive phenomena. In conclusion, these studies illustrate an approach for simultaneous mapping of the electronic and ionic transport on a single defective structure level such as dislocations or interfaces, and pave the way for creating libraries of defect-specific electrochemical responses.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Behavior of nanoceria in biologically-relevant environments

Cerium oxide nanoparticles (CNPs) have gained a considerable attention in biological research due to their anti-oxidant like behaviour and regenerative nature. The current literature on CNPs reports many successful attempts on harnessing the beneficial therapeutic properties in biology. However studies have also shown toxicity effect with some types of CNPs. This review discusses issues associated with the behaviours of CNPs in biological systems and identifies key knowledge gaps. We explore how salient physicochemical properties (size, surface chemistry, surface stabilizers) contribute to the potential positive and negative aspects of nanoceria in biological systems. Based on variations of results reported in the literature, important issues need to be addressed. Are we really studying the same particles with slight variations in size and physicochemical properties or do the particles being examined have fundamentally different behaviours? Are the variations observed in the result of differences in the initial properties of the particles or the results of downstream effects that emerge as the particles are prepared for specific studies and they interact with biological or other environmental moieties? How should particles be appropriately prepared for relevant environmental/toxicology/safety studies? It is useful to recognize that nanoparticles encompass some of the same complexities and variability associated with biological components

Environmental Molecular Sciences Laboratory↗

Real space mapping of ionic diffusion and electrochemical activity in energy storage and conversion materials

A method and system for probing mobile ion diffusivity and electrochemical reactivity on a nanometer length scale of a free electrochemically active surface includes a control module that biases the surface of the material. An electrical excitation signal is applied to the material and induces the movement of mobile ions. An SPM probe in contact with the surface of the material detects the displacement of mobile ions at the surface of the material. A detector measures an electromechanical strain response at the surface of the material based on the movement and reactions of the mobile ions. The use of an SPM tip to detect local deformations allows highly reproducible measurements in an ambient environment without visible changes in surface structure. The measurements illustrate effective spatial resolution comparable with defect spacing and well below characteristic grain sizes of the material.

25 ENERGY STORAGE↗

Performance study of polycrystalline CVD diamond detectors for fast neutron monitoring

Diamond detectors using polycrystalline CVD diamond substrates of thickness 300μm and 100μm were fabricated for fast neutron monitoring application.. The characterization of detectors was carried out using various tests such as leakage current, capacitance and alpha particle response. The performance of detectors was evaluated for fast neutrons at different neutron yields. The results presented in this work demonstrate that the diamond detectors will be suitable for monitoring fast neutrons.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

Mechanism of direct current electrical charge conduction in p-toluenesulfonate doped polypyrrole/carbon composites

Polypyrrole/carbon (PPy/C) composites have been synthesized using varying concentration of p-toluenesulfonate (pTS) dopant by surface initiated in-situ chemical oxidative polymerization. The synthesis and influence of pTS on the structure of the PPy/C composites are confirmed by Fourier transform infrared studies and the morphological features have been examined by scanning electron microscopy. X-ray photoelectron spectroscopy, employed to examine the surface composition and doping level of these composites, confirms the anionic doping into the polymer backbone. Electron spin resonance measurement has been carried out on these samples to identify the nature of the charge carriers and their concentration at different doping levels. The dc electrical conductivity of these composites has been measured in the temperature range ∼10–305 K. The observed results have been analyzed in the framework of existing theoretical models. Different Mott's parameters, such as characteristic temperature (T{sub 0}), density of states at the Fermi level (N(E{sub F})), average hopping distance (R), and average hopping energy (W), evaluated from dc conductivity data supports the applicability of Mott's three dimensional variable range hopping mechanism in this system.

36 MATERIALS SCIENCE↗

Epstein–Barr virus nuclear antigen 3C interact with p73: Interplay between a viral oncoprotein and cellular tumor suppressor

The p73 protein has structural and functional homology with the tumor suppressor p53, which plays an important role in cell cycle regulation, apoptosis, and DNA repair. The p73 locus encodes both a tumor suppressor (TAp73) and a putative oncogene (ΔNp73). p73 May play a significant role in p53-deficient lymphomas infected with Epstein–Barr virus (EBV). EBV produces an asymptomatic infection in the majority of the global population, but it is associated with several human B-cell malignancies. The EBV-encoded Epstein–Barr virus nuclear antigen 3C (EBNA3C) is thought to disrupt the cell cycle checkpoint by interacting directly with p53 family proteins. Doxorubicin, a commonly used chemotherapeutic agent, induces apoptosis through p53 and p73 signaling such that the lowΔNp73 level promotes the p73-mediated intrinsic pathway of apoptosis. In this report, we investigated the mechanism by which EBV infection counters p73α-induced apoptosis through EBNA3C. - Highlights: • EBV-encoded EBNA3C suppresses doxorubicin-induced apoptosis in B-cell lymphomas. • EBNA3C binds to p73 to suppress its apoptotic effect. • EBNA3C maintains latency by regulating downstream mitochondrial pathways.

60 APPLIED LIFE SCIENCES↗

In situ formation of micron-scale Li-metal anodes with high cyclability

Scanning probe microscopy methods have been used to fabricate and cycle micron-scale Li anodes deposited electrochemically under nanofabricated Au current collectors. An average Li volume of 5 10^8 nm3 was deposited and cycled with 100 % coulombic efficiency for ~ 160 cycles. Integrated charge/discharge values agree with before/after topography, as well as in situ dilatometry, suggesting this is a reliable method to study solid-state electrochemical processes. In this work we illustrate the possibility to deposit highly cyclable nanometer thick Li electrodes by mature SPM and nanofab techniques which can pave the way for inexpensive nanoscale battery arrays.

Arruda, Thomas M↗

Enhanced magnetoelectric sensitivity in Co{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–Bi{sub 0.9}La{sub 0.1}FeO{sub 3} nanocomposites

Graphical abstract: Polycrystalline nanocomposites of xCo{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–(1 − x)Bi{sub 0.9}La{sub 0.1}FeO{sub 3} (x = 0.1, 0.2, 0.3 and 0.4) were prepared by sol–gel method with average crystallite size in the range 70–80 nm as confirmed by AFM image. Magnetization (M) and magnetocapacitance (MC) were found to be enhanced for the nanocomposite. Highlights: ► Co{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–Bi{sub 0.9}La{sub 0.1}FeO{sub 3} nanocomposites (grain size ∼ 90 nm) prepared by sol–gel method. ► Magnetization (M) was found 4.5% more than 0.4CoFe{sub 2}O{sub 4}–0.6BiFeO{sub 3} composite. ► Magnetocapacitance (MC) is observed higher compared to Ba doped BiFeO{sub 3}. ► The value of α{sub E} was found to be 10% more than some reported. - Abstract: We report the magnetoelectric, dielectric and magnetic properties of xCo{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–(1 − x)Bi{sub 0.9}La{sub 0.1}FeO{sub 3} (x = 0.1, 0.2, 0.3 and 0.4) nanocomposites prepared by sol–gel method. The X-ray diffraction patterns of sintered pellets show the formation of composite phases. The average crystallite size obtain by Williamson–Hall plot for different nanocomposites were found to be in the range 70–80 nm, which are in agreement with particle size calculated from atomic force microscopy. Magnetoelectric voltage coefficient (α{sub E} = 315 mV/cm Oe) and the magnetocapacitance (MC = 3.1%) for x = 0.3 were found to be higher than other synthesized nanocomposites.

36 MATERIALS SCIENCE↗

Nanoscale Probing of Voltage Activated Oxygen Reduction/Evolution Reactions in Nanopatterned (LaxSr1-x)CoO3- Cathodes

Bias-dependent mechanisms of reversible and irreversible electrochemical processes on a (La0.5Sr0.5)2CoO4 modified (LaxSr1-x)CoO3- surface are studied using dynamic electrochemical strain microscopy (D-ESM). The reversible oxygen reduction/evolution process is activated at voltages as low as 3 4 V and the degree of transformation increases linearly with applied bias. The irreversible processes associated with static surface deformation become apparent above 10 12 V. Post-mortem focused-ion milling combined with atomic resolution scanning transmission electron microscopy and electron energy loss spectroscopy is used to establish the mechanisms of irreversible transformations and attribute it to amorphization of the top layer of material. These studies both establish the framework for probing irreversible electrochemical processes in solids and illustrate rich spectrum of electrochemical transformations underpinning electrocatalytic activity in cobaltites.

electrochemical strain microscopy↗

Spatially Resolved Mapping of Oxygen Reduction/evolution Reaction on Solid-Oxide Fuel Cell Cathodes with sub-10 nm Resolution

Spatial localization of the oxygen reduction/evolution reactions (ORR/OER) on lanthanum strontium cobaltite (LSCO) surfaces with perovskite and layered perovskite structures is studied on the sub-10 nanometer level. Comparison between Electrochemical Strain Microscopy (ESM) and structural imaging by scanning transmission electron microscopy (STEM) suggest that small-angle grain boundaries act as regions with enhanced electrochemical activity. The ESM activity is compared across a family of LSCO samples, demonstrating excellent agreement with macroscopic behaviors. This study potentially paves the way for deciphering the mechanisms of electrochemical activity of solids on the level of single extended structural defects such as grain boundaries and dislocations.

Electrochemical Strain microcsopy↗

Towards quantitative electrochemical measurements on the nanoscale by scanning probe microscopy: environmental and current spreading effects

The application of electric bias across tip-surface junctions in scanning probe microscopy can readily induce surface and bulk electrochemical processes that can be further detected though changes in surface topography, Faradaic or conductive currents, or electromechanical strain responses. However, the basic factors controlling tip-induced electrochemical processes, including the relationship between applied tip bias and the thermodynamics of local processes remains largely unexplored. Using the model Li-ion reduction reaction on the surface in Li-ion conducting glass ceramic, we explore the factors controlling Li-metal formation and find surprisingly strong effects of atmosphere and back electrode composition on the process. These studies suggest the feasibility of SPM-based quantitative electrochemical studies under proper environmental controls, extending the concepts of ultramicroelectrodes to the single-digit nanometer scale.

Arruda, Thomas M↗

Nanometer-scale mapping of irreversible electrochemical nucleation processes on solid Li-ion electrolytes

Electrochemical processes associated with changes in structure, connectivity or composition typically proceed via new phase nucleation with subsequent growth of nuclei. Understanding and controlling reactions requires the elucidation and control of nucleation mechanisms. However, factors controlling nucleation kinetics, including the interplay between local mechanical conditions, microstructure and local ionic profile remain inaccessible. Furthermore, the tendency of current probing techniques to interfere with the original microstructure prevents a systematic evaluation of the correlation between the microstructure and local electrochemical reactivity. In this work, the spatial variability of irreversible nucleation processes of Li on a Li-ion conductive glass-ceramics surface is studied with ,30 nm resolution. An increased nucleation rate at the boundaries between the crystalline AlPO4 phase and amorphous matrix is observed and attributed to Li segregation. This study opens a pathway for probing mechanisms at the level of single structural defects and elucidation of electrochemical activities in nanoscale volumes.

Kumar, Amit↗

Frequency spectroscopy of irreversible electrochemical nucleation kinetics

An approach is developed for probing the thermodynamics and kinetics of the irreversible electrochemical reactions on solid surfaces based on frequency-voltage spectroscopy. For a model Li-ion conductor surface, the two regimes for bias-controlled behavior are demonstrated and ascribed to the difference in the critical nucleus size. The electrostatic and electrochemical phenomena at tip-surface junction are analyzed. These studies suggest an experimental pathway for exploring local electrochemical activity in solids.

Kumar, Amit↗

Giant energy density in [001]-textured Pb(Mg1/3Nb2/3)O3-PbZrO3-PbTiO3 piezoelectric ceramics

Pb(Zr,Ti)O3 (PZT) based compositions have been challenging to texture or grow in a single crystal form due to the incongruent melting point of ZrO2. Here we demonstrate the method for achieving 90% textured PZT-based ceramics and further show that it can provide highest known energy density in piezoelectric materials through enhancement of piezoelectric charge and voltage coefficients (d and g). Our method provides more than 5 increase in the ratio d(textured)/d(random). A giant magnitude of d g coefficient with value of 59 000 10 15 m2 N 1 (comparable to that of the single crystal counterpart and 359% higher than that of the best commercial compositions) was obtained.

Yan, Yongke↗