A study on the kinetic arrest of magnetic phases in nanostructured Nd0.6Sr0.4MnO3thin films.

The Nd0.6Sr0.4MnO3(NSMO) manganite system exhibits a phase transition from paramagnetic insulating (PMI) to ferromagnetic metallic (FMM) state around its Curie temperatureTC= 270 K (bulk). The morphology-driven changes in the kinetically arrested magnetic phases in NSMO thin films with granular and crossed-nano-rod-type morphology are studied. The manganite thin films at low temperatures possess a magnetic glassy state arising from the coexistence of the high-temperature PMI and the low-temperature FMM phases. The extent of kinetic arrest and its relaxation was studied using the 'cooling and heating in unequal field (CHUF)' protocol in magnetic and magnetotransport investigations. The sample with rod morphology showed a large extent of phase coexistence compared to the granular sample. Further, with a field-cooling protocol, time-evolution studies were carried out to understand the relaxation of arrested magnetic phases across these morphologically distinct thin films. The results on the devitrification of the arrested magnetic state are interpreted from the point of view of homogeneous and heterogeneous nucleation of the ferromagnetic phase in the paramagnetic matrix with respect to temperature.

The effect of charged particle irradiation on the transport properties of bismuth chalcogenide topological insulators: a brief review.

Topological insulators (TIs) offer a novel platform for achieving exciting applications, such as low-power electronics, spintronics, and quantum computation. Hence, the spin-momentum locked and topologically nontrivial surface state of TIs is highly coveted by the research and development industry. Particle irradiation in TIs is a fast-growing field of research owing to the industrial scalability of the particle irradiation technique. Unfortunately, real three-dimensional TI materials, such as bismuth selenide, invariably host a significant population of charged native defects, which cause the ideally insulating bulk to behave like a metal, masking the relatively weak signatures of metallic topological surface states. Particle irradiation has emerged as an effective technique for Fermi energy tuning to achieve an insulating bulk in TI along with other popularly practiced methods, such as substitution doping and electrical gating. Irradiation methods have been used for many years to enhance the thermoelectric properties of bismuth chalcogenides, predominantly by increasing carrier density. In contrast, uncovering the surface states in bismuth-based TI requires the suppression of carrier density via particle irradiation. Hence, the literature on the effect of irradiation on bismuth chalcogenides extends widely to both ends of the spectrum (thermoelectric and topological properties). This review attempts to collate the available literature on particle irradiation-driven Fermi energy tuning and the modification of topological surface states in TI. Recent studies on particle irradiation in TI have focused on precise local modifications in the TI system to induce magnetic topological ordering and surface selective topological superconductivity. Promising proposals for TI-integrated circuits have also been put forth. The eclectic range of irradiation-based studies on TI has been reviewed in this manuscript.

High-Pressure Synthesis of Manganese Monocarbide: A Potential Superhard Material.

In this paper, we report for the first time formation of novel manganese monocarbide (MnC) using laser-heated diamond anvil cell (LHDAC). The synthesis was carried out at high pressure-high temperature (HPHT) and subsequently quenched to ambient condition. The formation and reproducibility have been confirmed in the pressure range of 4.7 to 9.2 GPa. Employing contribution of different probes viz.X-ray diffraction (XRD), selected area electron diffraction (SAED), and ab initio electronic structure calculation, the structure of MnC was found to be ZnS type i.e. a cubic lattice with a = 4.4294(2) Å. The bulk modulus has been determined to be 170(5) GPa from in situ high-pressure X-ray diffraction (HPXRD). Hardness of ZnS type MnC is estimated from an empirical relation to be about 40 GPa, making it a potential superhard material.

An insight into the origin of room-temperature ferromagnetism in SnO2 and Mn-doped SnO2 quantum dots: an experimental and DFT approach.

SnO2 and Mn-doped SnO2 single-phase tetragonal crystal structure quantum dots (QDs) of uniform size with control over dopant composition and microstructure were synthesized using the high pressure microwave synthesis technique. On a broader vision, we systematically investigated the influence of dilute Mn ions in SnO2 under the strong quantum confinement regime through various experimental techniques and density functional theoretical (DFT) calculations to disclose the physical mechanism governing the observed ferromagnetism. DFT calculations revealed that the formation of the stable (001) surface was much more energetically favorable than that of the (100) surface, and the formation energy of the oxygen vacancies in the stable (001) surface was comparatively higher in the undoped SnO2 QDs. X-ray photoelectron spectroscopy (XPS) and first-principles modeling of doped QDs revealed that the lower doping concentration of Mn favored the formation of MnO-like (Mn2+) structures in defect-rich areas and the higher doping concentration of Mn led to the formation of multiple configurations of Mn (Mn2+ and Mn3+) in the stable surfaces of SnO2 QDs. Electronic absorption spectra indicated the characteristic spin allowed ligand field transitions of Mn2+ and Mn3+ and the red shift in the band gap. DFT calculations clearly indicated that only the substitutional dopant antiferromagnetic configurations were more energetically favorable. The gradual increase of magnetization at a low level of Mn-doping could be explained by the prevalence of antiferromagnetic manganese-vacancy pairs. Higher concentrations of Mn led to the appearance of ferromagnetic interactions between manganese and oxygen vacancies. The increase in the concentration of metallic dopants caused not just an increase in the total magnetic moment of the system but also changed the magnetic interactions between the magnetic moments on the metal ions and oxygen. The present study provides new insight into the fundamental understanding of the origin of ferromagnetism in transition metal-doped QDs.

Tuning of the Thermoelectric Properties of Bi2Te3 Nanorods Using Helium Ion Irradiation.

The present study reports an enhancement of the power factor of Bi2Te3 nanorods NRs) by helium (He+) ion irradiation. High-resolution transmission electron microscopy studies revealed the formation of amorphous layers on the surface of the NRs at the high ion fluence. This amorphous nature is due to the accumulation of migrating point defect clusters at the surface of the NRs. Raman scattering experiments provide further insight to the observed structural modifications. At higher ion fluence, impurity-dominated scattering processes significantly enhance the value of the Seebeck coefficient of Bi2Te3 NRs. The He+ ion irradiation up to the ion fluence of 1 × 1016 ions/cm2 improves the thermoelectric transport properties with the highest power factor, 8.2 µW/m K2, at 390 K. Further investigations may result in the possibility of fabricating the Bi2Te3 NRs as thermoelectric generators with a high power factor for space applications.

Photoluminescence of oxygen vacancies and hydroxyl group surface functionalized SnO2 nanoparticles.

We report, for the first time, the luminescence property of the hydroxyl group surface functionalized quantum dots (QDs) and nanoparticles (NPs) of SnO2 using low energy excitations of 2.54 eV (488 nm) and 2.42 eV (514.5 nm). This luminescence is in addition to generally observed luminescence from 'O' defects. The as-prepared SnO2 QDs are annealed at different temperatures under ambient conditions to create NPs with varying sizes. Subsequently, the average size of the NPs is calculated from the acoustic vibrations observed at low frequencies in the Raman spectra and by the transmission electron microscopy measurements. Detailed photoluminescence studies with 3.815 eV (325 nm) excitation reveal the nature of in-plane and bridging 'O' vacancies as well as adsorption and desorption occurring at different annealing temperatures. X-ray photoelectron spectroscopy studies also support this observation. The defect level related to the surface -OH functional groups shows a broad luminescence peak at around 1.96 eV in SnO2 NPs which is elaborated using temperature dependent studies.

Quantification of oxide particle composition in model oxide dispersion strengthened steel alloys.

Oxide dispersion strengthened ferritic steels (ODS) are being considered for structural components of future designs of fission and fusion reactors because of their impressive high-temperature mechanical properties and resistance to radiation damage, both of which arise from the nanoscale oxide particles they contain. Because of the critical importance of these nanoscale phases, significant research activity has been dedicated to analysing their precise size, shape and composition (Odette et al., Annu. Rev. Mater. Res. 38 (2008) 471-503 [1]; Miller et al., Mater. Sci. Technol. 29(10) (2013) 1174-1178 [2]). As part of a project to develop new fuel cladding alloys in India, model ODS alloys have been produced with the compositions, Fe-0.3Y2O3, Fe-0.2Ti-0.3Y2O3 and Fe-14Cr-0.2Ti-0.3Y2O3. The oxide particles in these three model alloys have been studied by APT in their as-received state and following ion irradiation (as a proxy for neutron irradiation) at various temperatures. In order to adequately quantify the composition of the oxide clusters, several difficulties must be managed, including issues relating to the chemical identification (ranging and variable peak-overlaps); trajectory aberrations and chemical structure; and particle sizing. This paper presents how these issues can be addressed by the application of bespoke data analysis tools and correlative microscopy. A discussion follows concerning the achievable precision in these measurements, with reference to the fundamental limiting factors.

Valence state, hybridization and electronic band structure in the charge ordered AlV2O4.

The valence state, hybridization and electronic band structure of charge ordered AlV2O4 are investigated by measuring the electron energy loss spectra (EELS) and performing band structure calculations using the WIEN2k code. White line ratio and O K edges of V2O5, VO2, V2O3 and AlV2O4, obtained using electron energy loss spectroscopy, are analysed specifically to probe systematically the VO6 octahedra in all of them. The systematic decrease of the L2 intensity and the O K edge intensity from V(5+) in V2O5 to AlV2O4 indicates a progressive increase in the occupancy of the hybridized states, which is corroborated by the absence of a transition from O 1s to hybridized 2t(2g). Band structure calculations on the parent charge frustrated cubic phase and the charge ordered rhombohedral phase clearly document a band gap in the charge ordered state. From the structural information obtained after convergence and the spectroscopic information from EELS, it appears that partial orbital occupancy may lead to a deviation from an integral valence state on all the vanadium in this exotic charge ordered spinel system.

A high resolution scanning electron microscope for in situ investigation of swift heavy ion induced modification of solid surfaces.

A new in situ high resolution electron microscope (HRSEM) setup has been designed and integrated into the materials science beamline (M-branch) of the universal linear accelerator at Gesellschaft für Schwerionenforschung, Darmstadt for in situ investigations of swift heavy ion induced surface modifications. Special ports for in situ experiments are installed at the HRSEM chamber to connect it to the high vacuum beamline, which is equipped with suitable beam control and shaping devices. In order to demonstrate the feasibility and power of this new instrument, first experiments were performed on a 50-nm-thick Fe(2)O(3) film on Si substrate, which exhibited submicrometer size holes due to irradiation induced dewetting in a previous experiment. We have demonstrated that with our new instrument, the development of individual dewetting holes as a function of the ion fluence can be investigated and even the interaction between them can be studied. To illustrate pattern formation during grazing incidence, 3.6 MeV/u (131)Xe ion irradiation was carried out on a 25-nm-thick NiO film on SiO(2)/Si at a tilt angle of 75 degrees. The SEM image sequence recorded during the experiment reveals the development of a lamellaelike structure also seen before in ex situ experiments. With our new in situ setup, however, we are able to not only investigate the overall average pattern formation, but also to track the formation and decay of individual linking structures, which would be hardly possible in a standard ex situ experiment.

Implantation induced hardening of nanocrystalline titanium thin films.

Formation of nanocrystalline TiN at low temperatures was demonstrated by combining Pulsed Laser Deposition (PLD) and ion implantation techniques. The Ti films of nominal thickness approximatly 250 nm were deposited at a substrate temperature of 200 degrees C by ablating a high pure titanium target in UHV conditions using a nanosecond pulsed Nd:YAG laser operating at 1064 nm. These films were implanted with 100 keV N+ ions with fluence ranging from 1.0 x 10(16) ions/cm2 to 1.0 x 10(17) ions/cm2 The structural, compositional and morphological evolutions were tracked using Transmission Electron Microscopy (TEM), Secondary Ion Mass Spectrometry (SIMS) and Atomic Force Microscopy (AFM), respectively. TEM analysis revealed that the as-deposited titanium film is an fcc phase. With increasing ion fluence, its structure becomes amorphous phase before precipitation of nanocrystalline fcc TIN phase. Compositional depth profiles obtained from SIMS have shown the extent of nitrogen concentration gradient in the implantation zone. Both as-deposited and ion implanted films showed much higher hardness as compared to the bulk titanium. AFM studies revealed a gradual increase in surface roughness leading to surface patterning with increase in ion fluence.

Structure and photoluminescence properties of ion beam synthesized SiC nanoparticles in Si.

Silicon carbide nanoparticles were synthesized in Si(100) wafers by 300 keV C+ ion implantation at elevated substrate temperatures of 550, 650 and 700 degrees C. The implantation has been carried out upto a fluence of 2 x 10(17) ions/cm2 with a constant current density 1.2 microA/cm2. GIXRD analysis on the implanted sample confirms the formation of 3C-SiC. XTEM studies of sample implanted at 650 degrees C show that size of SiC nanoparticles is 6 nm at a depth 0.6 microm from the sample surface. PL spectrum of sample implanted at different temperatures showed a peak at 2.45 eV and 2.3 eV and the intensity of PL peak increases with implantation temperature. The peak at 2.45 eV corresponds to blue shifted emission from SiC nanoparticles having size 6 nm. The peak at 2.3 eV is assigned to the SiC nanoparticles with enhanced d-value.

Si(+) ion irradiation in a Co/Pt multilayer system.

This paper deals with a study of the effect of Si(+) ion irradiation on a Co/Pt multilayer system irradiated at different temperatures. The as-deposited and irradiated samples have been characterized using x-ray reflectivity (XRR), x-ray diffraction (XRD) and the magneto-optical Kerr effect (MOKE). X-ray reflectivity shows clear intermixing at the interfaces. The x-ray diffraction pattern shows that Si(+) ion irradiation at higher temperatures results in the formation of the CoPt(3) fcc phase with a small fraction of L1(0) phase. The mixing process is discussed in terms of recoil displacements induced by energy transfers from ions.