Colloidal Plasmonic Titanium Nitride Nanoparticles: Properties and Applications

Optical properties of colloidal plasmonic titanium nitride nanoparticles are examined with an eye on their photothermal via transmission electron microscopy and optical transmittance measurements. Single crystal titanium nitride cubic nanoparticles with an average size of 50 nm exhibit plasmon resonance in the biological transparency window. With dimensions optimized for efficient cellular uptake, the nanoparticles demonstrate a high photothermal conversion efficiency. A self-passivating native oxide at the surface of the nanoparticles provides an additional degree of freedom for surface functionalization.Comment: 17 pages, 4 figures, 1 abstract figur

Colloidal CuFeS2 Nanocrystals: Intermediate Fe d-Band Leads to High Photothermal Conversion Efficiency

We describe the colloidal hot-injection synthesis of phase-pure nanocrystals (NCs) of a highly abundant mineral, chalcopyrite (CuFeS2). Absorption bands centered at around 480 and 950 nm, spanning almost the entire visible and near infrared regions, encompass their optical extinction characteristics. These peaks are ascribable to electronic transitions from the valence band (VB) to the empty intermediate band (IB), located in the fundamental gap and mainly composed of Fe 3d orbitals. Laser-irradiation (at 808 nm) of an aqueous suspension of CuFeS2 NCs exhibited significant heating, with a photothermal conversion efficiency of 49%. Such efficient heating is ascribable to the carrier relaxation within the broad IB band (owing to the indirect VB-IB gap), as corroborated by transient absorption measurements. The intense absorption and high photothermal transduction efficiency (PTE) of these NCs in the so-called biological window (650-900 nm) makes them suitable for photothermal therapy as demonstrated by tumor cell annihilation upon laser irradiation. The otherwise harmless nature of these NCs in dark conditions was confirmed by in vitro toxicity tests on two different cell lines. The presence of the deep Fe levels constituting the IB is the origin of such enhanced PTE, which can be used to design other high performing NC photothermal agents.Comment: 12 pages, Chemistry of Materials, 31-May-201

Photothermal Conversion Characteristics of Silver Nanoparticle Dispersions

This paper was presented at the 4th Micro and Nano Flows Conference (MNF2014), which was held at University College, London, UK. The conference was organised by Brunel University and supported by the Italian Union of Thermofluiddynamics, IPEM, the Process Intensification Network, the Institution of Mechanical Engineers, the Heat Transfer Society, HEXAG - the Heat Exchange Action Group, and the Energy Institute, ASME Press, LCN London Centre for Nanotechnology, UCL University College London, UCL Engineering, the International NanoScience Community, www.nanopaprika.eu.Nanoparticle-based direct absorption system is a recent development, which employs nanoparticles to absorb and convert solar energy directly into thermal energy within the fluid volume. This work reports for the first time the use of plasomic nanoparticles (PNPs) to improve the direct photo-thermal conversion efficiency. Rod-shaped silver nanoparticles are synthesized and used as an example to illustrate the photo-thermal conversion characteristics of PNPs and the effect of particle shape. The result reveals a significant role of particle morphology on the photo-thermal conversion efficiency (PTE). For spherical silver particles, constant specific absorption rate (SAR), ~0.14 kW/g, is observed and the PTE increases nearly linearly with the particle concentration. For rod-shaped silver nanoparticles, much higher SARs (2~5 kW/g) are obtained, and the PTE increases from 43% (pure DI water) to 61% at a low concentration of 0.0028%. It is suggested that the increased specific surface area and the absorption spectrum variation are the two main reasons for the strong heating effect of rod-shaped silver nanoparticles

Functionalized MoS2 nanosheet-capped periodic mesoporous organosilicas as a multifunctional platform for synergistic targeted chemo-photothermal therapy

The combination of different therapies into a single platform has attracted increasing attention as a potential synergistic tumor treatment. Herein, the fabrication of a novel folate targeted system for chemo-photothermal therapy by using thioether-bridged periodic mesoporous organosilica nanoparticles (PMOs) as a drug-loading vehicle is described. The novel targeted molecular bovine serum albumin-folic acid-modified MoS2 sheets (MoS2-PEI-BSA-FA) were successfully synthesized and characterized, and then utilized as a capping agent to block PMOs to control the drug release and to investigate their potential in near-infrared photothermal therapy. The resulting PMOs–DOX@MoS2–PEI-BSA-FA complexes had a uniform diameter (196 nm); high DOX loading capacity (185 mg/g PMOs-SH); excellent photothermal transformation ability; and good biocompatibility in physiological conditions. The PMOs–DOX@MoS2–PEI-BSA-FA exhibited pH-dependence and near infrared (NIR) laser irradiation-triggered DOX release. In vitro experimental results confirmed that the material exhibits excellent photothermal transfer ability, outstanding tumor killing efficiency and specificity to target tumor cells via an FA-receptor-mediated endocytosis process. The in vivo experiments further demonstrated that the platform for synergistic chemo-photothermal therapy could significantly inhibit tumor growth, which is superior to any monotherapy. Meanwhile, cytotoxicity assays and histological assessments show that the engineered PMOs@MoS2–PEI-BSA-FA have good biocompatibility, further inspiring potential biomedical applications. Overall, this work describes an excellent drug delivery system for chemo-photothermal synergistic targeted therapy having good drug release properties, which have great potential in cancer therapy

Solar-driven broad spectrum fungicides based on monodispersed Cu₇S₄ nanorods with strong near-infrared photothermal efficiency

The development of low-cost and biocompatible inorganic photothermal nanoagents with broadband sunlight absorption and high photothermal conversion efficiency as broad spectrum fungicides is highly desirable for the large scale antibacterial treatment especially in the wild, because of their highly efficient anti-bacteria ability via solar irradiation. Here, we present a facile strategy for the synthesis of Cu7S4 nanorods (NRs) with broadband light absorption (300-3300 nm) and high photothermal conversion efficiency (57.8%, 808 nm), and the use of these NRs as broad spectrum fungicides for efficient disinfection using natural sunlight as light source. In the presence of Cu7S4 NRs, with natural sunlight irradiation (70 mW cm-2), both Gram-positive (S. aureus) and Gram-negative (E. coli) bacterium strains (2 mL, 106 mL-1) were completely killed in 10 min. These results suggest that our Cu7S4 NRs are effective and broad spectrum photothermal anti-bacterial agents regardless of drug resistance, that are particularly suitable for anti-bacteria activity in the wild using solar irradiation where artificial light sources are not available. Due to their strong near infrared (NIR) absorption, these biocompatible and low-cost Cu7S4 NRs may also serve as promising agents for photothermal therapy of tumors, disinfection in clinics, food sterilization and environmental treatment.</p

A general kinetic model for the photothermal oxidation of polypropylene

A general kinetic model for the photothermal oxidation of polypropylene has been derived from the basic auto-oxidation mechanistic scheme in which the main sources of radicals are the thermolysis and photolysis of the most unstable species, i.e hydroperoxides. Thermolysis is a uni- or bi-molecular reaction whose rate constant obeys an Arrhenius law. In contrast, photolysis is exclusively a unimolecular reaction and its rate constant is independent of temperature. According to the quantum theory, this latter is proportional to the energy absorbed by photosensitive species and thus, accounts for the impact of UV-light intensity and wavelength on the global oxidation kinetics. The validity of this model has been checked on iPP films homogeneously oxidized in air over a wide range of temperatures and UV-light sources. It gives access to the concentration changes of: (i) primary (hydroperoxides) and secondary (carbonyls) oxidation products, (ii) double bonds, (iii) chain scissions and crosslinking nodes, but also to the subsequent changes in molecular masses. These calculations are in full agreement with the photolysis results reported by Carlsson and Wiles in the 70s [1–3]. However, the model seems to be only valid for UV-light energies equivalent to about 10 suns as upper boundary, presumably because of multiphotonic excitations or chromophores photosensitization (i.e. termolecular photo-physical reactions), both enhanced at high irradiances