arXiv subjects

N. Ghafoor

Publications and source records attributed to N. Ghafoor.

6 recordsLinked to original sources

arXiv2025

Three-fold Superstructured Superlattice HfN/HfAlN Thin Films for Enhanced Toughness

To simultaneously achieve high hardness and high toughness in protective coatings remains a fundamental challenge. Here, we harness the superlattice architecture to combine Koehler hardening while the coherent interfaces reduce the crack driving force and improve toughness, enabling coatings that are both hard and damage tolerant. We design and fabricate epitaxial HfN$_{1.33}$/Hf$_{0.76}$Al$_{0.24}$N$_{1.15}$ superlattices, deposited on MgO(001) substrates using low-energy, high-flux ion-assisted reactive magnetron sputtering. These superlattices with bilayer periods ranging from 6 to 20 nm, exhibit a unique three-fold superstructure, confirmed by X-ray diffraction and reciprocal space mapping (RSM). Each constituent forms distinct 3D checkerboard superstructures, with a period of 7.5 {\AA} for HfN and 12.5 A for HfAlN. RSMs further reveal low mosaicity, high crystalline quality, and in-plane compressive strains, indicating well preserved coherence across interfaces. Mechanical testing shows that the superlattices maintain the high hardness of HfAlN (\~36 GPa) independent of bilayer period, while surpassing the softer HfN (~27 GPa), consistent with interface-driven Koehler strengthening. Micropillar compression shows brittle fracture on the {110}<110> system, yet with distributed cracking and faster mechanical recovery compared to monolithic films, suggesting improved toughness. Cube-corner indentation further corroborate this behavior, with pile-up and suppressed fracture events. These results demonstrate that epitaxial HfN/HfAlN superlattices uniquely combine high hardness with improved toughness, enabled by their three-fold superstructured architecture. Leveraging the intrinsic high-temperature stability of HfN-based materials, this design offers a robust pathway toward next-generation protective coatings capable of maintaining performance under extreme conditions.

cond-mat.mtrl-sci↗

arXiv2025

Growth Mechanisms and Mechanical Response of 3D Superstructured Cubic and Hexagonal Hf$_{1-x}$Al$_x$N Thin Films

Transition metal aluminum nitrides are a technologically important class of multifunctional ceramics, however, the HfAlN system remains largely unexplored. We investigate phase stability, nanostructure design, and mechanical behavior of Hf$_{1-x}$Al$_x$N$_y$ thin films deposited on MgO(001) substrates using ion-assisted reactive magnetron sputtering. Compared to growth temperature and ion assistance, backscattered Ar neutrals are shown to have a dominant influence on the film structure. The Al-rich (x > 0.41) films form a nanocrystalline morphology consisting of Hf- and Al-rich nanodomains in a wurtzite-hexagonal(h) 0001 fiber-texture exhibiting about 22 GPa hardness, considerably higher than that of a binary AlN. For low Al contents, x < 0.30, surface-driven spinodal decomposition by energetic Ar neutrals during deposition in combination with quenching of sub-surface diffusion results in an unusual - and unique for nitrides - three-dimensional checkerboard superstructure of AlN- and HfN-rich nanodomains in the single-crystal rocksalt-cubic (c) phase. Lattice-resolved scanning transmission electron microscopy complemented with x-ray and electron diffraction reveals that the superstructure periodicity extends along <100> directions and the size increases linearly from 9 to 13 A with rising Al content. Consequently, the nanoindentation hardness increases sharply from 26 GPa for HfN$_y$, to \~38 GPa for c-Hf$_{1-x}$Al$_x$N$_y$, due to dislocation pinning at the superstructure strain fields. Micropillar compression of c-Hf$_{0.93}$Al$_{0.07}$N$_{1.15}$ shows a considerably higher yield stress compared to HfN$_y$ and controlled brittle fracture occurs via {110}<011> slip systems, attributed to superstructure inhibited dislocation motion. In contrast, nanocrystalline h-Hf$_{0.59}$Al$_{0.41}$N$_{1.23}$ exhibits a high yield stress and limited plasticity before strain burst failure.

cond-mat.mtrl-sci↗

arXiv2024

Eliminating the spin-down critical angle in polarizing neutron optics for expanding the polarization bandwidth

Polarized neutron scattering is a very important analysis technique for studies of magnetism, spintronics, and high-sensitivity measurements, among others, offering invaluable information. Yet, the efficiency of such experiments rely on the performance of the polarizing neutron optics to provide high reflectivity and polarization. Presently, state-of-the-art polarizers like Fe/Si supermirrors are not able to polarize neutrons at low scattering angles in a monochromatic beam or able to polarize neutrons with a variety of wavelengths as for a non-monochromatic beam. To overcome this limitation, it is suggested to use Co/Ti multilayers on Ti substrates owing to their favorable scattering length density characteristics. It is shown that this approach enables a wavelength bandwidth several times larger than achievable with state-of-the-art materials on Si or glass substrates. Consequently, enabling the possibility of polarizing neutrons across an extended wavelength range, including those with very high wavelengths.

cond-mat.mtrl-sci↗

arXiv2024

Chemically homogeneous boron carbide 10B/11B isotope modulated neutron interference mirrors

We introduce a novel type of neutron interference mirrors based on a chemically homogeneous BxC (x>4) matrix with internal high precision 10B/11B isotope modulation. Simulations predict that these mirrors exhibit very high neutron reflectivities for a small number of bilayer periods. This is experimentally confirmed by neutron reflectivity measurements of mirrors synthesized by ion-assisted magnetron sputter deposition. For example, a 120 nm thick multilayer consisting of just 20 bilayer periods of 10B5.7C/11B5.7C, with a periodicity of 61.5 Å, exhibits a neutron reflectivity of 13 percent at an incidence angle of 4.7 deg for neutrons with a wavelength of 4.825 Å. This is attributed to a high scattering length density contrast between the layers with an interface width <5 Å. Structural analyses by X-ray diffraction, X-ray reflectivity, and transmission electron microscopy demonstrate that the 10B5.7C/11B5.7C multilayer mirrors are composed of amorphous, chemically homogenous B5.7C, without any internal chemical modulation. The data show that 10BxC/11BxC multilayer mirrors have the potential for higher neutron reflectivities at higher q-values using fewer and thinner layers, compared to todays state-of-the-art chemically modulated neutron multilayer mirrors.

cond-mat.mtrl-sci↗

arXiv2024

Neutron optical tuning of Fe/11B4CTi multilayers for optimal polarization and increased reflectivity for polarizing neutron optics

The concept of scattering length density tuning for improved polarization is investigated for Fe/11B4CTi multilayers and compared to the commonly used Fe/Si system in polarizing multilayer neutron optics. X-ray and neutron reflectivity, magnetization, and neutron polarization have been measured on such multilayers, highlighting differences from conventional Fe/Si multilayers. The multilayer systems were deposited with 25 Å period thickness, a layer thickness ratio of 0.35 and 20 periods, using ion-assisted DC magnetron sputtering. Replacing Si with 11B4CTi for these multilayers showed an increase in reflectivity due to a reduction in interface width. By tuning the ratio between 11B4C and Ti in the non-magnetic layers, a broad range of scattering length density values was achieved, facilitating scattering length density contrast matching between layers for spin-down neutrons, thereby enhancing polarization. These findings demonstrate the potential of Fe/11B4CTi multilayers as a promising option for polarizing neutron optics and highlight the concept of scattering length density tuning in a large range using 11B4CTi.

cond-mat.mtrl-sci↗

arXiv2023

Reflective, polarizing, and magnetically soft amorphous Fe/Si multilayer neutron optics with isotope-enriched 11B4C inducing atomically flat interfaces

The utilization of polarized neutrons is of great importance in scientific disciplines spanning materials science, physics, biology, and chemistry. Polarization analysis offers insights into otherwise unattainable sample information such as magnetic domains and structures, protein crystallography, composition, orientation, ion-diffusion mechanisms, and relative location of molecules in multicomponent biological systems. State-of-the-art multilayer polarizing neutron optics have limitations, particularly low specular reflectivity and polarization at higher scattering vectors/angles, and the requirement of high external magnetic fields to saturate the polarizer magnetization. Here, we show that by incorporating 11B4C into Fe/Si multilayers, amorphization and smooth interfaces can be achieved, yielding higher neutron reflectivity, less diffuse scattering and higher polarization. Magnetic coercivity is eliminated, and magnetic saturation can be reached at low external fields (>2 mT). This approach offers prospects for significant improvement in polarizing neutron optics, enabling; nonintrusive positioning of the polarizer, enhanced flux, increased data accuracy, and further polarizing/analyzing methods at neutron scattering facilities.

cond-mat.mtrl-sci↗