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Justinas Palisaitis

Publications and source records attributed to Justinas Palisaitis.

6 recordsLinked to original sources

Synthesis of Ti2B2Clx MBenes in molten salts from theoretical and experimental perspectives

The unique properties and application possibilities of two-dimensional (2D) materials motivates the exploration of different nanolaminated compounds. Here, by using a molten salt approach, we selectively etch Ti2InB2 with ZnCl2 to produce a multilayer (ml) Ti2B2Clx MBene. Scanning transmission electron microscopy, in combination with energy dispersive X-ray, and electron energy loss spectroscopies show that In atoms are completely removed from the precursor upon etching, being replaced by chlorine surface terminations with a coverage 1.1 < x < 1.4. Further, in situ X-ray diffraction indicates a direct biphasic transformation from Ti2InB2 to ml-MBene, with no signs of intermediate phase formation. A computational framework based on density functional theory further corroborates these experimental observations by showing a negative reaction free energy for the formation of ml-MBene, favourable over all competing processes. In addition, A-element substitution into to the 3D Ti2ZnB2 phase is predicted to be endergonic, consistent with the absence of experimental evidence for its formation. Initial Li-ion battery performance evaluation showed a stable discharge capacity similar or better than MAX phases and other borides. Altogether, the theoretical framework combined with materials synthesis and characterization provides a general approach for 2D materials development, for further expansion of the family of 2D materials.

cond-mat.mtrl-sci↗

Atomistic mechanism and interface-structure-energetics of van der Waals epitaxy demonstrated by layered alpha-MoO3 growth on mica

Unlike conventional epitaxy, van der Waals epitaxy (vdWE) allows nearly stress-free growth of thick films with highly oriented crystals without dislocations even for large film-substrate lattice mismatches. Despite reports of vdWE in numerous materials systems, an atomistic understanding of film/substrate interface structure that explains and predicts vdWE has remained elusive. Here, we address this knowledge gap by unveiling atomistic interface mechanisms for vdWE of alpha-MoO3(0k0) on mica(001). X-ray diffraction and electron microscopy reveal alpha-MoO3(0k0) epilayers with large columnar crystals in three non-equivalent in-plane orientations. These results, together with negligible strain buildup in continuous epilayers, confirm vdWE. Ab initio computations showing interface energy minima for these orientations correlate with high cross-interface proximity between Mo atoms in alpha-MoO3 and K in mica conducive for maximal vdW attraction. These atomistic insights on interface structure and energetics provide a crucial framework for predicting vdWE for different film/substrate combinations and designing of stress-free and/or standalone epitaxial films of layered materials such as MoO3 on layered substrates such as f-mica.

cond-mat.mtrl-sci↗

Enzyme-free in situ polymerization of conductive polymers catalyzed by porous Au@Ag nanowires for stretchable neural electrodes

In situ polymerization of conductive polymers (CPs) represents a transformative approach in bioelectronics, by enabling the controlled growth of electrically active materials right at the tissue or device surface to create seamless biotic-abiotic interfaces. Traditional CP deposition techniques often use high anodic potentials, non-physiological electrolytes, or strong oxidants, making them harmful to adjacent tissues. A possible solution is enzymatic polymerization which operates under milder conditions, but it is limited by the stability and activity window of the enzyme catalysts, low throughput, and challenges in spatially confining polymer growth. To resolve these issues, here we developed one-dimensional porous Au-coated Ag nanowires with horseradish peroxidase (HRP)-like catalytic properties, thereby for the first time enabling mild in situ enzyme-free polymerization of conductive polymers near neutral pH. The enzyme-free polymerization is demonstrated both in aqueous dispersions at pH=6 and in situ onto porous Au coated Ag nanowire based stretchable electrodes. Following enzyme-free catalytic polymerization, the electrically conducting polymer coating on the electrode greatly improves the impedance and achieves an impedance of 2.6 kOhm at 1 kHz for 50x50 um large electrodes.

physics.chem-ph↗

The Role of 11B4C Interlayers in Enhancing Fe/Si Multilayer Performance for Polarized Neutron Mirrors

This study investigates the effects of incorporating 11B4C interlayers into Fe/Si multilayers, with a focus on interface quality, reflectivity, polarization, and magnetic properties for polarized neutron optics. It is found that the introduction of 1 Å and 2 Å 11B4C interlayers significantly improves the interface sharpness, reducing interface width and preventing excessive Si diffusion into the Fe layers. X-ray reflectivity and polarized neutron reflectivity measurements show enhanced reflectivity and polarization, with a notable increase in polarization for 30 Å period multilayers. The inclusion of interlayers also helps prevent the formation of iron-silicides, improving both the magnetic properties and neutron optical performance. However, the impact of interlayers is less pronounced in thicker-period multilayers (100 Å), primarily due to the ratio between layer and interface widths. These results suggest that 11B4C interlayers offer a promising route for optimizing Fe/Si multilayer performance in polarized neutron mirrors.

cond-mat.mtrl-sci↗

Chemical-scissor-mediated structural editing of layered transition metal carbides

Intercalation of non-van der Waals (vdW) layered materials can produce new 2D and 3D materials with unique properties, but it is difficult to achieve. Here, we describe a structural editing protocol for 3D non-vdW layered ternary carbides and nitrides (MAX phases) and their 2D vdW derivatives (MXenes). Gap-opening and species-intercalating stages were mediated by chemical scissors and guest intercalants, creating a large family of layered materials with unconventional elements and structures in MAX phases, as well as MXenes with versatile termination species. Removal of surface terminations by metal scissors and stitching of carbide layers by metal atoms leads to a reverse transformation from MXenes to MAX phases, and metal-intercalated 2D carbides. This scissor-mediated structural editing may enable structural and chemical tailoring of other layered ceramics.

cond-mat.mtrl-sci↗

Solid-state Janus nanoprecipitation enables amorphous-like heat conduction in crystalline Mg3Sb2-based thermoelectric materials

Solid-state precipitation can be used to tailor materials properties, ranging from ferromagnets and catalysts to mechanical strengthening and energy storage. Thermoelectric properties can be modified by precipitation to enhance phonon scattering while retaining charge-carrier transmission. Here, we uncover unconventional dual Janus-type nanoprecipitates in Mg3Sb1.5Bi0.5 formed by side-by-side Bi- and Ge-rich appendages, in contrast to separate nanoprecipitate formation. These Janus nanoprecipitates result from local co-melting of Bi and Ge during sintering, enabling an amorphous-like lattice thermal conductivity. A precipitate size effect on phonon scattering is observed due to the balance between alloy-disorder and nanoprecipitate scattering. The thermoelectric figure-of-merit ZT reaches 0.6 near room temperature and 1.6 at 773 K. The Janus nanoprecipitation can be introduced into other materials and may act as a general property-tailoring mechanism.

cond-mat.mtrl-sci↗