557-07-3Relevant articles and documents
Scalable Synthesis of InAs Quantum Dots Mediated through Indium Redox Chemistry
Ginterseder, Matthias,Franke, Daniel,Perkinson, Collin F.,Wang, Lili,Hansen, Eric C.,Bawendi, Moungi G.
supporting information, p. 4088 - 4092 (2020/03/04)
Next-generation optoelectronic applications centered in the near-infrared (NIR) and short-wave infrared (SWIR) wavelength regimes require high-quality materials. Among these materials, colloidal InAs quantum dots (QDs) stand out as an infrared-active candidate material for biological imaging, lighting, and sensing applications. Despite significant development of their optical properties, the synthesis of InAs QDs still routinely relies on hazardous, commercially unavailable precursors. Herein, we describe a straightforward single hot injection procedure revolving around In(I)Cl as the key precursor. Acting as a simultaneous reducing agent and In source, In(I)Cl smoothly reacts with a tris(amino)arsenic precursor to yield colloidal InAs quantitatively and at gram scale. Tuning the reaction temperature produces InAs cores with a first excitonic absorption feature in the range of 700-1400 nm. A dynamic disproportionation equilibrium between In(I), In metal, and In(III) opens up additional flexibility in precursor selection. CdSe shell growth on the produced cores enhances their optical properties, furnishing particles with center emission wavelengths between 1000 and 1500 nm and narrow photoluminescence full-width at half-maximum (FWHM) of about 120 meV throughout. The simplicity, scalability, and tunability of the disclosed precursor platform are anticipated to inspire further research on In-based colloidal QDs.
Multistage Microfluidic Platform for the Continuous Synthesis of III–V Core/Shell Quantum Dots
Baek, Jinyoung,Shen, Yi,Lignos, Ioannis,Bawendi, Moungi G.,Jensen, Klavs F.
supporting information, p. 10915 - 10918 (2018/08/01)
We present a fully continuous chip microreactor-based multistage platform for the synthesis of quantum dots with heterostructures. The use of custom-designed chip reactors enables precise control of heating profiles and flow distribution across the microfluidic channels while conducting multistep reactions. The platform can be easily reconfigured by reconnecting the differently designed chip reactors allowing for screening of various reaction parameters during the synthesis of nanocrystals. III–V core/shell quantum dots are chosen as model reaction systems, including InP/ZnS, InP/ZnSe, InP/CdS and InAs/InP, which are prepared in flow using a maximum of six chip reactors in series.
Lethal photosensitisation of Staphylococcus aureus and Escherichia coli using crystal violet and zinc oxide-encapsulated polyurethane
Sehmi, Sandeep K.,Noimark, Sacha,Bear, Joseph C.,Peveler, William J.,Bovis, Melissa,Allan, Elaine,MacRobert, Alexander J.,Parkin, Ivan P.
, p. 6490 - 6500 (2015/08/06)
Crystal violet and zinc oxide nanoparticles (CVZnO) were incorporated into medical grade polyurethane polymers by a two-step dipping procedure to prepare novel bactericidal surfaces. The photobactericidal activity of CVZnO polyurethane samples was tested against the Gram-positive bacterium, Staphylococcus aureus and the Gram-negative bacterium, Escherichia coli. Exposure of the polymer samples to white light induced the lethal photosensitisation of both S. aureus and E. coli. In addition, this novel system demonstrated significant antibacterial activity under dark conditions against S. aureus within 2 hours, but more remarkably, a 99.9% reduction in the numbers of E. coli within 4 hours in the dark. This is, to the best of our knowledge, the most potent 'dark-kill' by a light activated antimicrobial agent ever reported. The singlet oxygen quenchers, bovine serum albumin and l-histidine, and an enzyme which catalyses the decomposition of hydrogen peroxide, bovine catalase, were incorporated into the antibacterial assays to determine if the mechanism of E. coli kill involved a Type 1 or a Type 2 light-activated process.
