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Sz-Chian Liou

Publications and source records attributed to Sz-Chian Liou.

5 recordsLinked to original sources

Unraveling atomic-resolution valence electron energy-loss spectroscopic imaging in a single-crystal CaNb2O6

Despite advancements in electron optics and spectrometer design over the past twenty years, atomic-resolution valence-electron energy-loss spectroscopy imaging remains challenging due to the delocalization of inelastic electron scattering. In this study, we used an energy-filtered spectrometer equipped with a hybrid-pixel direct electron detector and spherical aberration-corrected scanning transmission electron microscopy to analyze many-electron excitations and interband transitions in a single-crystal calcium niobate, CaNb2O6, with spatial resolution ranging from the nanometers to the atomic scale. In the low-loss region above the bandgap at about 3.8 eV, we observed volume plasmons, around 6 eV and 15 eV energy loss, as well as a mix of strongly correlated plasmons and excitons, known as plexcitons, at approximately 7.3 eV energy loss. Additionally, we employed an on-axis EELS setup for atomic-resolution zero-loss peak (ZLP) imaging and visualized energy- and atom-resolved images of plexcitons and VPs, which showed contrast reversal relative to high-angle annular dark-field images. To investigate elastic contrast preservation, we also analyzed the effect of the collection angle and minimized its influence to produce delocalized VP images. In fact, the ZLP and VEELS images obtained using the weak-beam setup demonstrate that, in both cases, the contrast resembles Z-contrast. Moreover, we found that [NbO6] octahedra directly contributed to the lateral maps of interband transitions in the range from 3.2 eV to 3.5 eV energy loss. These findings demonstrate that Cs-STEM-EELS, which examines atomic-scale contrast associated with low-energy losses, can be a powerful tool for visualizing the structure, bonding, and electronic properties of complex crystalline nanostructures, including individual atomic sites, interstitial sites, and point defects.

cond-mat.mtrl-sci↗

Accelerated intermetallic phase amorphization in a Mg-based high-entropy alloy powder

We describe a novel mechanism for the synthesis of a stable high-entropy alloy powder from an otherwise immiscible Mg-Ti rich metallic mixture by employing high-energy mechanical milling. The presented methodology expedites the synthesis of amorphous alloy powder by strategically injecting entropic disorder through the inclusion of multi-principal elements in the alloy composition. Predictions from first principles and materials theory corroborate the results from microscopic characterizations that reveal a transition of the amorphous phase from a precursor intermetallic structure. This transformation, characterized by the emergence of antisite disorder, lattice expansion, and the presence of nanograin boundaries, signifies a departure from the precursor intermetallic structure. Additionally, this phase transformation is accelerated by the presence of multiple principal elements that induce severe lattice distortion and a higher configurational entropy. The atomic size mismatch of the dissimilar elements present in the alloy produces a stable amorphous phase that resists reverting to an ordered lattice even on annealing.

cond-mat.mtrl-sci↗

Synergistically creating sulfur vacancies in semimetal-supported amorphous MoS2 for efficient hydrogen evolution

The presence of elemental vacancies in materials is inevitable according to statistical thermodynamics, which will decide the chemical and physical properties of the investigated system. However, the controlled manipulation of vacancies for specific applications is a challenge. Here we report a facile method for creating large concentrations of S vacancies in the inert basal plane of MoS2 supported on semimetal CoMoP2. With a small applied potential, S atoms can be removed in the form of H2S due to the optimized free energy of formation. The existence of vacancies favors electron injection from the electrode to the active site by decreasing the contact resistance. As a consequence, the activity is increased by 221 % with the vacancy-rich MoS2 as electrocatalyst for hydrogen evolution reaction (HER). A small overpotential of 75 mV is needed to deliver a current density of 10 mA cm-2, which is considered among the best values achieved for MoS2. It is envisaged that this work may provide a new strategy for utilizing the semimetal phase for structuring MoS2 into a multi-functional material.

cond-mat.mtrl-sci↗

Superconductivity and magnetism in Iron Sulfides Intercalated by Metal Hydroxides

Inspired by naturally occurring sulfide minerals, we present a new family of iron-based superconductors. A metastable form of FeS known as the mineral mackinawite forms two-dimensional sheets that can be readily intercalated by various cationic guest species. Under hydrothermal conditions using alkali metal hydroxides, we prepare three different cation and metal hydroxide-intercalated FeS phases including (Li$_{1-x}$Fe$_x$OH)FeS, [(Na$_{1-x}$Fe$_x$)(OH)$_2$]FeS, and K$_x$Fe$_{2-y}$S$_2$. Upon successful intercalation of the FeS layer, the superconducting critical temperature $T_c$ of mackinawite is enhanced from 5 K to 8 K for the (Li$_{1-x}$Fe$_x$OH)$^{δ+}$ intercalate. Layered heterostructures of [(Na$_{1-x}$Fe$_x$)(OH)$_2$]FeS resemble the natural mineral tochilinite, which contains an iron square lattice interleaved with a hexagonal hydroxide lattice. Whilst heterostructured [(Na$_{1-x}$Fe$_x$)(OH)$_2$]FeS displays long-range magnetic ordering near 15 K, K$_x$Fe$_{2-y}$S$_2$ displays short range antiferromagnetism.

cond-mat.supr-con↗

Flux dependent MeV self-ion- induced effects on Au nanostructures: Dramatic mass transport and nano-silicide formation

We report a direct observation of dramatic mass transport due to 1.5 MeV Au2+ ion impact on isolated Au nanostructures of an average size 7.6 nm and a height 6.9 nm that are deposited on Si (111) substrate under high flux (3.2x10^10 to 6.3x10^12 ions cm-2 s-1) conditions. The mass transport from nanostructures found to extend up to a distance of about 60 nm into the substrate, much beyond their size. This forward mass transport is compared with the recoil implantation profiles using SRIM simulation. The observed anomalies with theory and simulations are discussed. At a given energy, the incident flux plays a major role in mass transport and its re-distribution. The mass transport is explained on the basis of thermal effects and creation of rapid diffusion paths at nano-scale regime during the course of ion irradiation. The unusual mass transport is found to be associated with the formation of gold silicide nanoalloys at sub-surfaces. The complexity of the ion-nanostructure interaction process has been discussed with a direct observation of melting (in the form of spherical fragments on the surface) phenomena. The transmission electron microscopy, scanning transmission electron microscopy and Rutherford backscattering spectroscopy methods have been used.

cond-mat.mtrl-sci↗