We demonstrate amyloid fibril (AF) decomposition induced by NIR-active upconversion nanoparticles complexed with photosensitisers. The process is triggered by upconversion, which initiates a photochemical reaction cascade that culminates in the generation of the highly reactive singlet-oxygen product 1O2 close to the amyloid superstructures, resulting in AF decomposition.
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http://dx.doi.org/10.1039/c9pp00356h | DOI Listing |
ACS Appl Mater Interfaces
January 2024
Functional Material Group, AMP Division, CSIR-National Metallurgical Laboratory, Jamshedpur 831007, India.
A wide solar light absorption window and its utilization, long-term stability, and improved interfacial charge transfer are the keys to scalable and superior solar photocatalytic performance. Based on this objective, a noble metal-free composite photocatalyst is developed with conducting MXene (TiC) and semiconducting cauliflower-shaped CdS and porous CuO. XPS, HRTEM, and ESR analyses of TiO@TiC confirm the formation of enough defect-enriched TiO (where is < 2) on the surface of TiC during hydrothermal treatment, thus creating a third semiconducting site with enough oxygen vacancy.
View Article and Find Full Text PDFPhotochem Photobiol Sci
January 2020
Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo, 162-8601, Japan.
We demonstrate amyloid fibril (AF) decomposition induced by NIR-active upconversion nanoparticles complexed with photosensitisers. The process is triggered by upconversion, which initiates a photochemical reaction cascade that culminates in the generation of the highly reactive singlet-oxygen product 1O2 close to the amyloid superstructures, resulting in AF decomposition.
View Article and Find Full Text PDFACS Nano
January 2020
Department of Materials Science, WW4-LKO , University of Erlangen-Nuremberg, 91058 Erlangen , Germany.
The low penetration depth of UV light in mammalian tissue is the critical limitation for the use of TiO-based photocatalysis in biomedical applications. In this work, we develop an effective near-infrared (NIR)-active photocatalytic platform that consists of a shell structure of upconversion nanocrystals decorated on a core of Au/dark-TiO. The heart of this system is the strong photocatalytic activity in the visible region enabled by the gold surface-plasmon resonance on dark TiO (D-TiO).
View Article and Find Full Text PDFNanoscale
December 2019
School of Materials Science and Engineering (SMSE), Gwangju Institute of Science and Technology (GIST), 123 Cheomdangwagi-ro, Buk-gu, Gwangju 61005, Republic of Korea.
As an alternative to silicon-based solar cells, organic-inorganic hybrid perovskite solar cells (PSCs) have attracted much attention and achieved a comparable power conversion efficiency (PCE) to silicon-based ones, although the perovskite materials can absorb only visible light. Hence, the challenge remains to enhance the PCE utilizing near infrared (NIR) light in the solar light spectrum. One of the easiest ways to utilize the NIR is to incorporate NIR active materials in PSCs such as up-conversion nanoparticles (UCNPs); however, such a stratergy is not simple to adopt in PSCs due to the inherent vurnerability of perovskite materials towards moisture.
View Article and Find Full Text PDFACS Appl Bio Mater
November 2018
Department of Chemistry and Nano Science, Division of Molecular and Life Sciences, College of Natural Sciences, Ewha Womans University, Seoul 03760, Korea.
The development of high-performance near-infrared (NIR) photocatalysts with long-term stability and the elucidation on the working mechanism along with multifunctional activity toward biomedical applications have not been explored sufficiently. Herein, a novel hybrid material of an upconversion nanoparticle (NaYF/Yb,Er) (UCN) coated with a ternary semiconductor (AgInS, AIS) has been synthesized by a simple and robust two-step solvothermal route for NIR light active photocatalysis. Preparation of oleic acid-capped spherical UC nanoparticles (NPs) (∼25 nm) followed by solvothermal decomposition of two precursor complexes Ag(acda) and In(acda) resulted in the formation of well-defined NaYF/Yb,Er@AgInS core-shell nanoparticles (UCN@AIS NPs) (∼90 nm).
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