arXiv subjects

Yuki Orikasa

Publications and source records attributed to Yuki Orikasa.

6 recordsLinked to original sources

arXiv2024

Exploring $\rm Mg^{2+}$ and $\rm Ca^{2+}$ Conductors Via Solid-State Metathesis Reactions

The scarcity of viable electrode and electrolyte materials vastly hinders the advancement of magnesium and calcium batteries. This study utilises solid-state metathetical reactions involving chalcogen- and pnictogen-based honeycomb layered oxides with alkaline-earth halides/nitrates to synthesise $\rm Mg^{2+}$- and $\rm Ca^{2+}$-based materials previously achievable only under high-temperature/high-pressure conditions, as well as new metastable materials with unique crystal versatility. Particularly, we employ metathetical reactions involving $\rm Li_4MgTeO_6$, $\rm Na_2Mg_2TeO_6$, and $\rm Na_4MgTeO_6$ with $\rm MgCl_2$/$\rm MgSO_4$/$\rm Mg(NO_3)_2$.$\rm 6H_2O$ or $\rm Ca(NO_3)_2$.$\rm 4H_2O$ / $\rm CaCl_2$.$\rm 2H_2O$ at temperatures not exceeding 500 $^\circ$C to produce $\rm Mg_3TeO_6$ polymorphs, ilmenite-type $\rm CaMg_2TeO_6$/$\rm Mg_2CaTeO_6$, and double perovskite-type $\rm Ca_2MgTeO_6$. Thus, we demonstrate that these materials, conventionally requiring gigascale pressures or high temperatures (>1000$^\circ$C) for their proper synthesis, are now readily accessible at ambient pressure and considerably lower temperatures. Meanwhile, despite sub-optimal pellet densities, the synthesised ilmenite-type \magenta {$\rm Mg_3TeO_6$ (high-pressure polymorph)} and double perovskite-type ${\rm Ca}_2M{\rm TeO_6}$ ($M = \rm Mg, Ca, Zn$) materials exhibit remarkable bulk ionic conductivity at room temperature, marking them as promising compositional spaces for exploring novel $\rm Mg^{2+}$ and $\rm Ca^{2+}$ conductors. Furthermore, this study extends the applicability of metathetical reactions to attain Mg- or Ca-based antimonates, ruthenates, titanates, phosphates, and silicates, thus opening avenues to novel high-entropy multifunctional nanomaterial platforms with utility in energy storage and beyond.

cond-mat.mtrl-sci↗

arXiv2023

Honeycomb Layered Frameworks with Metallophilic Bilayers

This Review highlights the exciting advancements in the science of honeycomb layered frameworks with metallophilic bilayers that have recently garnered attention particularly due to reports of anomalous fractional valency states of silver cations sandwiched between transition metal slabs of other cations. First, the latest tactics and techniques including but not limited to X-ray absorption spectroscopy (XAS) and high-resolution transmission electron microscopy (HRTEM) particularly necessary for characterising recent honeycomb layered frameworks with metallophilic bilayers are described, with emphasis on silver-based oxides. Second, new strategies and concepts related to topochemically- or temperature-induced cationic-deficient phases expanding the compositional space of honeycomb layered frameworks focused on cationic bilayer architectures are also accentuated. Third, the latest condensed matter theoretic advances towards a full, atomistic description of the bilayered structure in such frameworks are detailed, especially related to critical phenomena at the cusp of the monolayer-bilayer phase transition. This entails, in part, describing honeycomb layered frameworks as optimised lattices within the congruent sphere packing problem, equivalent to a particular two-dimensional (2D) conformal field theory. Altogether, it is hoped that this Review will give the reader a panoramic view of the honeycomb layered frameworks with important applications within the emerging field of quantum matter, potentially redefining their frontier. Thus, the scope of this Review is expected to be worthwhile for recent graduates and emerging experts alike not only in the materials science and chemistry community but also in other diverse fields of interest.

cond-mat.mtrl-sci↗

arXiv2022

Honeycomb Layered Oxides With Silver Atom Bilayers and Emergence of Non-Abelian SU(2) Interactions

Honeycomb layered oxides with monovalent or divalent, monolayered cationic lattices generally exhibit myriad crystalline features encompassing rich electrochemistry, geometries and disorders, which particularly places them as attractive material candidates for next-generation energy storage applications. Herein, we report global honeycomb layered oxide compositions, ${\rm Ag_2}M_2{\rm TeO_6}$ ($M = \rm Ni, Mg, \textit{etc}.$) exhibiting $\rm Ag$ atom bilayers with sub-valent states within Ag-rich crystalline domains of ${\rm Ag_6}M_2{\rm TeO_6}$ and $\rm Ag$-deficient domains of ${\rm Ag}_{2 - x}\rm Ni_2TeO_6$ ($0 < x < 2$). The $\rm Ag$-rich material characterised by aberration-corrected transmission electron microscopy reveals local atomic structural disorders characterised by aperiodic stacking and incoherency in the bilayer arrangement of $\rm Ag$ atoms. Meanwhile, the global material not only displays high ionic conductivity, but also manifests oxygen-hole electrochemistry during silver-ion extraction. Within the $\rm Ag$-rich domains, the bilayered structure, argentophilic interactions therein and the expected $\rm Ag$ sub-valent states ($1/2+, 2/3+, \textit{etc}.$) are theoretically understood via spontaneous symmetry breaking of SU($2$)$\times$U($1$) gauge symmetry interactions amongst $3$ degenerate mass-less chiral fermion states, justified by electron occupancy of silver $4d_{z^2}$ and $5s$ orbitals on a bifurcated honeycomb lattice. This implies that bilayered frameworks have research applications that go beyond the confines of energy storage.

cond-mat.mtrl-sci↗

arXiv2022

A Potential Cathode Material for Rechargeable Potassium-Ion Batteries Inducing Manganese Cation and Oxygen Anion Redox Chemistry: Potassium-Deficient $\rm K_{0.4}Fe_{0.5}Mn_{0.5}O_2$

Potassium-ion ($\rm K$-ion) rechargeable batteries; considered to be lucrative low-cost battery options for large-scale and capacious energy storage systems, have been garnering tremendous attention in recent years. However, due to the scarcity of cathode materials that can condone the reversible re-insertion of the large $\rm K$-ions at feasible capacities, the viability of $\rm K$-ion batteries has been greatly undercut. In this paper, we explore a potential cathode material in the $\rm K_2O$-$\rm Fe_2O_3$-$\rm MnO_2$ ternary phase system, that not only demonstrates reversible $\rm K$-ion reinsertion but also manifests relatively fast rate capabilities. The titled cathode compound, $\rm K_{0.4}Fe_{0.5}Mn_{0.5}O_2$, demonstrates a reversible capacity of approximately $\rm120 $ mAh g$^{-1}$ at $\rm 10$ hours of (dis)charge ($viz.$, $\rm C/10$ rate) with $ca.$ $\rm 85$% of the capacity being retained at a $\rm 1$ hour of (dis)charge ($\rm 1 C$ rate) which is considered to be good capacity retention. Additionally, both hard and soft X-rays have been employed to unravel the mechanism by which $\rm K$-ion is reversibly inserted into $\rm K_{0.4}Fe_{0.5}Mn_{0.5}O_2$. The results revealed a cumulative participation of both manganese cations and oxygen anions in $\rm K_{0.4}Fe_{0.5}Mn_{0.5}O_2$ illustrating its potential as a high-capacity $\rm K$-ion battery cathode material that relies on both anion and cation redox. Further development of related high-capacity cathode compositions can be anticipated.

cond-mat.mtrl-sci↗

arXiv2019

Identification of ferrimagnetic orbitals preventing spinel degradation by charge ordering in Li$_x$Mn$_2$O$_4$

Spinel Li$_x$Mn$_2$O$_4$ is a key cathode material that is used extensively in commercial Li-ion batteries. A challenge with this material has been that the capacity of the battery fades with cycling, an effect that can be traced to the presence of an anti-ferromagnetic insulator phase in the fully lithiated LiMn$_2$O$_4$ (LMO) and the associated charge disproportionation that drives distortions of the MnO$_6$ octahedra. Here, by combining x-ray magnetic Compton scattering experiments with parallel first-principles computations, we show that the anti-ferromagnetic phase of LMO is surrounded by a robust ferrimagnetic metallic phase, which becomes stable when even a small amount of Li is removed from or added to the charge-ordered LMO. In this surprising ferrimagnetic state, charge-ordering and octahedral distortions are found to be strongly suppressed. We identify the nature of the ferrimagnetic orbitals involved through theoretical and experimental analyses of the magnetic Compton scattering spectra.

cond-mat.mtrl-sci↗

arXiv2017

In-operando quantitation of Li concentration for commercial Li-ion rechargeable battery using high-energy X-ray Compton scattering

Compton scattering is one of the promising probe to quantitate of the Li under in-operando condition, since high-energy X-rays which have high penetration power into the materials are used as incident beam and Compton scattered energy spectrum have specific line-shape by the elements. We develop in-operando quantitation method of Li composition in the electrodes by using line-shape (Sparameter) analysis of Compton scattered energy spectrum. In this study, we apply S-parameter analysis to commercial coin cell Li-ion rechargeable battery and obtain the variation of S-parameters during charge/discharge cycle at positive and negative electrodes. By using calibration curves for Li composition in the electrodes, we determine the change of Li composition of positive and negative electrodes through S-parameters, simultaneously.

physics.app-ph↗