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Yu Ogawa

Publications and source records attributed to Yu Ogawa.

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Tuning the morphology of aerosolised cellulose nanocrystals via controlled aggregation

Cellulose nanocrystals (CNCs) are polycrystalline, rod-shaped nanoparticles isolated from cellulose, which have attracted increasing attention for a wide variety of applications. While there has been significant research into CNCs in suspensions, hydrogels and films, there have been remarkably few studies that investigated their properties during and after aerosolisation. Here, we studied how aerosolisation impacts the size and morphology of different CNCs suspensions with different surface functionalities. By building a new experimental setup, we observed that colloidally-metastable aqueous CNC suspensions, achieved by carboxylation of the surface hydroxy groups or by exposure to high intensity ultrasonication, yield large particulates upon aerosolisation under ambient temperatures. In contrast, aqueous suspensions of unfunctionalised CNCs tend to produce, upon aerosolisation, smaller particulates, despite suffering from poor colloidal stability in liquid suspension. Our results demonstrate that both the aerosolisation process itself and the properties of the CNC suspension play a crucial role in determining the final particle size and morphology of CNC-based particles, highlighting the need to consider colloidal stability and surface functionality when designing CNC-based materials for applications involving aerosol delivery or spray drying.

cond-mat.soft

Tailoring the Morphology of Cellulose Nanocrystals via Controlled Aggregation

Cellulose nanocrystals (CNCs) are elongated nanoparticles derived from natural cellulose, with potential applications ranging from rheological modifiers and emulsion stabilizers to photonic pigments and sensors. For most applications, precise control over CNC morphology and surface chemistry is essential, but the relationship between process parameters, CNC characteristics, and their resulting behavior is poorly understood. Here, we investigate the impact of centrifugation and ionic strength on CNC morphology after dialysis using transmission electron microscopy, small-angle X-ray scattering and scanning electron diffraction. We find that the centrifugation step commonly applied during CNC purification promotes the formation of compact composite nanoparticles made of aligned crystallites, referred to as 'bundles', that are associated preferentially along their hydrophobic faces. In stark contrast, transient exposure to high ionic strength leads to fractal-like, irregular composite nanoparticles. We then examine the consequence of these morphological differences on the cholesteric self-organization of the CNCs: aligned bundles reduce the cholesteric pitch in suspension, causing a blue-shift in the color of dish-cast photonic films, while misaligned particles promote gelation, producing colorless films. This study reveals the importance of sample history, in particular, the often-disregarded purification steps, on CNC characteristics and their ensemble behavior, thereby unlocking new routes for tailoring this promising nanomaterial.

cond-mat.soft

Photo-excitation band-structure engineering of 2H-NbSe$_2$ probed by time- and angle-resolved photoemission spectroscopy

We investigated the nonequilibrium electronic structure of 2H-NbSe$_2$ by time- and angle-resolved photoemission spectroscopy. We find that the band structure is distinctively modulated by strong photo-excitation, as indicated by the unusual increase in the photoelectron intensities around E$_F$. In order to gain insight into the observed photo-induced electronic state, we performed DFT calculations with modulated lattice structures, and found that the variation of the Se height from the Nb layer results in a significant change in the effective mass and band gap energy. We further study the momentum-dependent carrier dynamics. The results suggest that the relaxation is faster at the K-centered Fermi surface than at the $Γ$-centered Fermi surface, which can be attributed to the stronger electron-lattice coupling at the K-centered Fermi surface. Our demonstration of band structure engineering suggests a new role for light as a tool for controlling the functionalities of solid-state materials.

cond-mat.str-el

Photo-induced semimetallic states realised in electron-hole coupled insulators

Using light to manipulate materials into desired states is one of the goals in condensed matter physics, since light control can provide ultrafast and environmentally-friendly photonics devices. However, it is generally difficult to realise a photo-induced phase which is not merely a higher entropy phase corresponding to a high-temperature phase at equilibrium. Here, we report realization of photo-induced insulator-to-metal transitions in Ta2Ni(Se1-xSx)5 including the excitonic insulator phase using time- and angle-resolved photoemission spectroscopy. From the dynamic properties of the system, we determine that screening of excitonic correlations plays a key role in the timescale of the transition to the metallic phase, which supports the existence of an excitonic-insulator phase at equilibrium. The non-equilibrium metallic state observed unexpectedly in the direct-gap excitonic insulator opens up a new avenue to optical band engineering in electron-hole coupled systems.

cond-mat.mtrl-sci

Antiphase Fermi-surface modulations accompanying displacement excitation in a parent compound of iron-based superconductors

We investigate the transient electronic structure of BaFe2As2, a parent compound of iron-based superconductors, by time- and angle-resolved photoemission spectroscopy. In order to probe the entire Brillouin zone, we utilize extreme ultraviolet photons and observe photoemission intensity oscillation with the frequency of the A1g phonon which is antiphase between the zone-centered hole Fermi surfaces (FSs) and zone-cornered electron FSs. We attribute the antiphase behavior to the warping in one of the zone-centered hole FSs accompanying the displacement of the pnictogen height, and find that this displacement is the same direction as that induced by substitution of P for As, where superconductivity is induced by a structural modification without carrier doping in this system.

cond-mat.supr-con