Titus Masese 교수

Rechargeable potassium-ion batteries have been gaining traction as not only promising low-cost alternatives to lithium-ion technology, but also as high-voltage energy storage systems. However, their development and sustainability are plagued by the lack of suitable electrode materials capable of allowing the reversible insertion of the large potassium ions. Here, exploration of the database for potassium-based materials has led us to discover potassium ion conducting layered honeycomb frameworks

Abstract The world is at the cusp of a new era where pivotal importance is being attached to the development of sustainable and high‐performance energy storage systems. Potassium‐ion batteries are deemed not only cheap battery candidates, but also as the penultimate high‐voltage energy storage systems within monovalent‐cation chemistries. However, their performance and sustainability are undermined by the lack of suitable electrolytes for high‐voltage operation, particularly owing to the limited

The advent of nanotechnology has hurtled the discovery and development of nanostructured materials with stellar chemical and physical functionalities in a bid to address issues in energy, environment, telecommunications and healthcare. In this quest, a class of two-dimensional layered materials consisting of alkali or coinage metal atoms sandwiched between slabs exclusively made of transition metal and chalcogen (or pnictogen) atoms arranged in a honeycomb fashion have emerged as materials exhib

The designing of high voltage cathode materials is critical for the advancement of potassium-ion (K-ion) battery. Herein, we present a new honeycomb framework P2-type K2/3Ni1/3Co1/3Te1/3O2 (or equivalently written as K2NiCoTeO6) which exhibits the highest voltage on record (beyond 4 V versus K+/K) for layered cathode materials. This work will allow for the further development of, particularly, high voltage layered cathodes for K-ion battery.

Li2FeSiO4 is a promising cathode material for lithium ion batteries because of its theoretically high capacity if two lithium ions can be extracted/inserted per formula unit; however, the extraction/insertion of two lithium ions from Li2FeSiO4 remains a challenge. Herein, we successfully synthesized carbon-coated Li2FeSiO4 nanoparticles which exhibit a capacity commensurate to a reversible two-lithium extraction/insertion at elevated temperature. This study investigates the mechanism underlying

Li2FeSiO4 is considered a promising cathode material for the next-generation Li-ion battery systems owing to its high theoretical capacity and low cost. Li2FeSiO4 exhibits complex polymorphism and undergoes significant phase transformations during charge and discharge reaction. To elucidate the phase transformation mechanism, crystal structural changes during charge and discharge processes of Li2FeSiO4 at different rates were investigated by X-ray diffraction measurements. The C/50 rate of lithi

Separators are key safety components for electrochemical energy storage systems. However, the intrinsic poor wettability with electrolyte and low thermal stability of commercial polyolefin separators cannot meet the requirements of the ever-expanding market for high-power, high-energy, and high-safety power systems, such as lithium-metal, lithium-sulfur, and lithium-ion batteries. In this study, scalable bendable networks built with ultralong silica nanowires (SNs) are developed as stable separa

Mn-based layered oxides have been considered the most promising cathode candidates for cost-effective potassium-ion batteries (PIBs). Herein, equiatomic constituents of Ni, Fe, Mg, and Ti have been introduced into the transition metal layers of Mn-based layered oxide to design a high-entropy K_0.6Ni_0.05Fe_0.05Mg_0.05Ti_0.05Mn_0.0725O₂ (HE-KMO, <i>S</i> = 1.17R). Consequently, the experimental results manifest that the layere

Honeycomb layered oxides constitute an emerging class of materials that show interesting physicochemical and electrochemical properties. However, the development of these materials is still limited. Here, we report the combined use of alkali atoms (Na and K) to produce a mixed-alkali honeycomb layered oxide material, namely, NaKNi₂TeO₆. Via transmission electron microscopy measurements, we reveal the local atomic structural disorders characterised by aperiodic stacking and

This perspective highlights progress in the development of cathode materials for potassium-ion batteries, whilst providing valuable insights into unexplored compositional spaces that can be pursued for high-performance electrode materials.

Endowed with a multitude of exquisite properties such as rich electrochemistry, superb topology and eccentric electromagnetic phenomena, honeycomb layered oxides have risen to the top echelons of science with applications in diverse fields ranging from condensed matter physics, solid-state chemistry, materials science, solid-state ionics to electrochemistry. However, these oxides are vastly underutilised as their underlying atomistic mechanisms remain unexplored. Therefore, in this study, atomic

To enhance the utilization of sulfur in lithium-sulfur batteries, three-dimensional tungsten nitride (WN) mesoporous foam blocks are designed to spatially localize the soluble Li₂S₆ and Li₂S₄ within the pore spaces. Meanwhile, the chemisorption behaviors of polysulfides and the capability of WN as an effective confiner are systematically investigated through density functional theory calculations and experimental studies. The theoretical calculations r

Potassium‐ion (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 allow the reversible reinsertion of large K‐ions at feasible capacities, the viability of K‐ion batteries has been greatly undercut. Herein, a potential cathode material is explored in the K 2 O–Fe 2 O 3 –MnO 2 ternary phase system