National Institute of Advanced Industrial Science and Technology

About: National Institute of Advanced Industrial Science and Technology is a government organization based out in Tsukuba, Ibaraki, Japan. It is known for research contribution in the topics: Catalysis & Thin film. The organization has 22114 authors who have published 65856 publications receiving 1669827 citations. The organization is also known as: Sangyō Gijutsu Sōgō Kenkyū-sho.

Light-driven liquid metal nanotransformers for biomedical theranostics.

Abstract: Room temperature liquid metals (LMs) represent a class of emerging multifunctional materials with attractive novel properties. Here, we show that photopolymerized LMs present a unique nanoscale capsule structure characterized by high water dispersibility and low toxicity. We also demonstrate that the LM nanocapsule generates heat and reactive oxygen species under biologically neutral near-infrared (NIR) laser irradiation. Concomitantly, NIR laser exposure induces a transformation in LM shape, destruction of the nanocapsules, contactless controlled release of the loaded drugs, optical manipulations of a microfluidic blood vessel model and spatiotemporal targeted marking for X-ray-enhanced imaging in biological organs and a living mouse. By exploiting the physicochemical properties of LMs, we achieve effective cancer cell elimination and control of intercellular calcium ion flux. In addition, LMs display a photoacoustic effect in living animals during NIR laser treatment, making this system a powerful tool for bioimaging.

Nanoarchitectured Structure and Surface Biofunctionality of Mesoporous Silica Nanoparticles

Abstract: Mesoporous silica nanoparticles (MSNs), one of the important porous materials, have garnered interest owing to their highly attractive physicochemical features and advantageous morphological attributes. They are of particular importance for use in diverse fields including, but not limited to, adsorption, catalysis, and medicine. Despite their intrinsic stable siliceous frameworks, excellent mechanical strength, and optimal morphological attributes, pristine MSNs suffer from poor drug loading efficiency, as well as compatibility and degradability issues for therapeutic, diagnostic, and tissue engineering purposes. Collectively, the desirable and beneficial properties of MSNs have been harnessed by modifying the surface of the siliceous frameworks through incorporating supramolecular assemblies and various metal species, and through incorporating supramolecular assemblies and various metal species and their conjugates. Substantial advancements of these innovative colloidal inorganic nanocontainers drive researchers in promoting them toward innovative applications like stimuli (light/ultrasound/magnetic)-responsive delivery-associated therapies with exceptional performance in vivo. Here, a brief overview of the fabrication of siliceous frameworks, along with discussions on the significant advances in engineering of MSNs, is provided. The scope of the advancement in terms of structural and physicochemical attributes and their effects on biomedical applications with a particular focus on recent studies is emphasized. Finally, interesting perspectives are recapitulated, along with the scope toward clinical translation.

Spin-orbit coupling in molecules: Chemistry beyond the adiabatic approximation

Abstract: An extensive introduction to spin-orbit coupling (SOC) is presented, starting from a discussion of the phenomenological operators and general chemical importance of SOC to studies of chemical reactions. Quantitative SOC operators are discussed, and the symmetry properties of the SOC Hamiltonian important for understanding the general features of SOC are summarized. Comparison of the one- and two-electron contributions to SOC is given, followed by a discussion of commonly used approximations for the two-electron part. Applications of SOC to studies using effective and model core potentials have been analysed. The theoretical discussion is illustrated with numerous practical examples, including diatomic molecules (with an emphasis on hydrides) and some examples for polyatomic molecules. The fine structure of the SOC interaction (vibrational dependence) for some diatomic molecules has been elucidated.

Recent progress in the phase-transition mechanism and modulation of vanadium dioxide materials

Abstract: Metal-to-insulator transition (MIT) behaviors accompanied by a rapid reversible phase transition in vanadium dioxide (VO2) have gained substantial attention for investigations into various potential applications and obtaining good materials to study strongly correlated electronic behaviors in transition metal oxides (TMOs). Although its phase-transition mechanism is still controversial, during the past few decades, people have made great efforts in understanding the MIT mechanism, which could also benefit the investigation of MIT modulation. This review summarizes the recent progress in the phase-transition mechanism and modulation of VO2 materials. A representative understanding on the phase-transition mechanism, such as the lattice distortion and electron correlations, are discussed. Based on the research of the phase-transition mechanism, modulation methods, such as element doping, electric field (current and gating), and tensile/compression strain, as well as employing lasers, are summarized for comparison. Finally, discussions on future trends and perspectives are also provided. This review gives a comprehensive understanding of the mechanism of MIT behaviors and the phase-transition modulations. Smart coatings that alter their electrical properties on demand can be created from shape-shifting vanadium dioxide (VO2) crystals. Xun Cao from Shanghai Institute of Ceramics, Chinese Academy of Sciences in Shanghai and co-workers review efforts to understand the mechanisms that enable VO2 to rapidly switch between two crystal states — one with metallic conductivity, the other insulating—at near-room temperature conditions. Theoretical calculations and nanoscale experiments reveal that VO2 transitions are triggered by a combination of interactions between electrons and atoms in the crystal lattice, and through forces that cause electrons to avoid each other. Several innovative methods of manipulating the VO2 switching temperature have emerged including foreign element additions, laser irradiation, and controlled substrate bending. The sensitivity of VO2 transitions to mechanical stress has inspired proposals for ultrafast response breath sensors and artificial skin. In this article, we review the prototypical phase-transition material-VO2, which undergoes structure and conductivity changes simultaneously. The recent progresses in the transition mechanism are also discussed. Besides, this work gives a comprehensive understanding of the phase-transition modulations, such as element doping, electric field (current and gating) and tensile/compression strain, as well as employing laser.

Photochemical reduction of CO₂ using TiO₂: effects of organic adsorbates on TiO₂ and deposition of Pd onto TiO₂.

Abstract: Reduction of CO(2) using semiconductors as photocatalysts has recently attracted a great deal of attention again. The effects of organic adsorbates on semiconductors on the photocatalytic products are noteworthy. On untreated TiO(2) (P-25) particles a considerable number of organic molecules such as acetic acid were adsorbed. Although irradiation of an aqueous suspension of this TiO(2) resulted in the formation of a significant amount of CH(4) as a major product, it was strongly suggested that its formation mainly proceeded via the photo-Kolbe reaction of acetic acid. Using TiO(2) treated by calcination and washing procedures for removal of the organic adsorbates, CO was photocatalytically generated as a major product, along with a very small amount of CH(4), from an aqueous suspension under a CO(2) atmosphere. In contrast, by using Pd (>0.5 wt %) deposited on TiO(2) (Pd-TiO(2)) on which organic adsorbates were not detected, CH(4) was the main product, but CO formation was drastically reduced compared with that on the pretreated TiO(2). Experimental data, including isotope labeling, indicated that CO(2) and CO(3)(2-) are the main carbon sources of the CH(4) formation, which proceeds on the Pd site of Pd-TiO(2). Prolonged irradiation caused deactivation of the photocatalysis of Pd-TiO(2) because of the partial oxidation of the deposited Pd to PdO.