In situ TEM oxidation study of Fe thin-film transformation to single-crystal magnetite nanoparticles

In this work, we present an in situ transmission electron microscopy (TEM) study of Fe thin films to Fe nanoparticle formation and their oxidation to single-crystal magnetite nanoparticles. Amorphous Fe thin films were prepared by sputtering on TEM carbon grids. The thin Fe films were continuously heated in situ from room temperature to 700 °C under vacuum (4 × 10–4 Pa). With the increase in temperature, the continuity of the thin film starts breaking, and Fe nanoparticle nucleation centers are formed. At 600 °C, the thin film transforms into metallic Fe nanoparticles (NPs) with a small presence of different Fe oxide NPs. Further increase in the temperature to 700 °C resulted in the full oxidation of the NPs (i.e., no core–shell were found). Zero-loss energy filtered diffraction and HRTEM analysis of the lattice spacing reveals that all NPs have fully transformed into single-phase magnetite NPs. The structural study of the magnetite NPs shows that magnetite NPs are free of antiphase domain boundary defects. This work demonstrates that under low partial pressure of oxygen at elevated temperatures a complete oxidation of Fe NPs into magnetite single-crystal nanoparticles can be achieved

Highly-excited Rydberg excitons in synthetic thin-film cuprous oxide

S.S. acknowledges support from the Swedish Research Council (Starting Grant No. 2019-04821) and from the Göran Gustafsson Foundation. H.A. acknowledges the Purdue University Startup fund, the financial support from the Industry-University Cooperative Research Center Program at the US National Science Foundation under Grant No. 2224960, and the AirForce Office of Scientific Research under award number FA9550-23-1-0489.Cuprous oxide (Cu2O) has recently emerged as a promising material in solid-state quantum technology, specifically for its excitonic Rydberg states characterized by large principal quantum numbers (n). The significant wavefunction size of these highly-excited states (proportional to n2) enables strong long-range dipole-dipole (proportional to n4) and van der Waals interactions (proportional to n11). Currently, the highest-lying Rydberg states are found in naturally occurring Cu2O. However, for technological applications, the ability to grow high-quality synthetic samples is essential. The fabrication of thin-film Cu2O samples is of particular interest as they hold potential for observing extreme single-photon nonlinearities through the Rydberg blockade. Nevertheless, due to the susceptibility of high-lying states to charged impurities, growing synthetic samples of sufficient quality poses a substantial challenge. This study successfully demonstrates the CMOS-compatible synthesis of a Cu2O thin film on a transparent substrate that showcases Rydberg excitons up to n=8 which is readily suitable for photonic device fabrications. These findings mark a significant advancement towards the realization of scalable and on-chip integrable Rydberg quantum technologies.Publisher PDFPeer reviewe

Site-Specific Wetting of Iron Nanocubes by Gold Atoms in Gas-Phase Synthesis

A key challenge in nanotechnology is the rational design of multicomponent materials that beat the properties of their elemental counterparts. At the same time, when considering the material composition of such hybrid nanostructures and the fabrication process to obtain them, one should favor the use of nontoxic, abundant elements in view of the limited availability of critical metals and sustainability. Cluster beam deposition offers a solvent- and, therefore, effluent-free physical synthesis method to achieve nanomaterials with tailored characteristics. However, the simultaneous control of size, shape, and elemental distribution within a single nanoparticle in a small-size regime (sub-10 nm) is still a major challenge, equally limiting physical and chemical approaches. Here, a single-step nanoparticle fabrication method based on magnetron-sputtering inert-gas condensation is reported, which relies on selective wetting of specific surface sites on precondensed iron nanocubes by gold atoms. Using a newly developed Fe-Au interatomic potential, the growth mechanism is decomposed into a multistage model implemented in a molecular dynamics simulation framework. The importance of growth kinetics is emphasized through differences between structures obtained either experimentally or computationally, and thermodynamically favorable configurations determined via global optimization techniques. These results provide a roadmap for engineering complex nanoalloys toward targeted applications.Peer reviewe

In situ chemoresistive sensing in the environmental TEM: probing functional devices and their nanoscale morphology

In situ transmission electron microscopy provides exciting opportunities to address fundamental questions and technological aspects related to functional nanomaterials, including the structure-property relationships of miniaturized electronic devices. Herein, we report the in situ chemoresistive sensing in the environmental transmission electron microscope (TEM) with a single SnO2 nanowire device, studying the impact of surface functionalization with heterogeneous nanocatalysts. By detecting toxic carbon monoxide (CO) gas at ppm-level concentrations inside the microscope column, the sensing properties of a single SnO2 nanowire were characterized before and after decoration with hybrid Fe-Pd nanocubes. The structural changes of the supported nanoparticles induced by sensor operation were revealed, enabling direct correlation with CO sensing properties. Our novel approach is applicable for a broad range of functional nanomaterials and paves the way for future studies on the relationship between chemoresistive properties and nanoscale morphology

Nanoscale Heterogeneity of Multilayered Si Anodes with Embedded Nanoparticle Scaffolds for Li-Ion Batteries

A new approach on the synthesis of Si anodes for Li‐ion batteries is reported, combining advantages of both nanoparticulated and continuous Si films. A multilayered configuration prototype is proposed, comprising amorphous Si arranged in nanostructured, mechanically heterogeneous films, interspersed with Ta nanoparticle scaffolds. Particular structural features such as increased surface roughness, nanogranularity, and porosity are dictated by the nanoparticle scaffolds, boosting the lithiation process due to fast Li diffusion and low electrode polarization. Consequently, a remarkable charge/discharge speed is reached with the proposed anode, in the order of minutes (1200 mAh g−1 at 10 C). Moreover, nanomechanical heterogeneity self‐limits the capacity at intermediate charge/discharge rates; as a consequence, exceptional cycleability is observed at 0.5 C, with 100% retention over 200 cycles with 700 mAh g−1. Higher capacity can be obtained when the first cycles are performed at 0.2 C, due to the formation of microislands, which facilitate the swelling of the active Si. This study indicates a method to tune the mechanical, morphological, and electrochemical properties of Si electrodes via engineering nanoparticle scaffolds, paving the way for a novel design of nanostructured Si electrodes for high‐performance energy storage devices

Tuning the onset of ferromagnetism in heterogeneous bimetallic nanoparticles by gas phase doping

In the nanoregime, chemical species can reorganize in ways not predicted by their equilibrium bulk behavior. Here, we engineer Ni-Cr nanoalloys at the magnetic end of their compositional range (i.e., 0–15 at. % Cr), and we investigate the effect of Cr incorporation on their structural stability and resultant magnetic ordering. To ensure their stoichiometric compositions, the nanoalloys are grown by cluster beam deposition, a method that allows one-step, chemical-free fabrication of bimetallic nanoparticles. While full Cr segregation toward nanoparticle surfaces is thermodynamically expected for low Cr concentrations, metastability occurs as the Cr dopant level increases in the form of residual Cr in the core region, yielding desirable magnetic properties in a compensatory manner. Using nudged elastic band calculations, residual Cr in the core is explained based on modifications in the local environment of individual Cr atoms. The resultant competition between ferromagnetic and antiferromagnetic ordering gives rise to a wide assortment of interesting phenomena, such as a cluster-glass ground state at very low temperatures and an increase in Curie temperature values. We emphasize the importance of obtaining the commonly elusive magnetic nanophase diagram for M-Cr (M=Fe, Co, and Ni) nanoalloys, and we propose an efficient single-parameter method of tuning the Curie temperature for various technological applications.Peer reviewe