Acetone Sensing and Catalytic Conversion by Pd-Loaded SnO2.

Noble metal additives are widely used to improve the performance of metal oxide gas sensors, most prominently with palladium on tin oxide. Here, we photodeposit different quantities of Pd (0-3 mol%) onto nanostructured SnO2 and determine their effect on sensing acetone, a critical tracer of lipolysis by breath analysis. We focus on understanding the effect of operating temperature on acetone sensing performance (sensitivity and response/recovery times) and its relationship to catalytic oxidation of acetone through a packed bed of such Pd-loaded SnO2. The addition of Pd can either boost or deteriorate the sensing performance, depending on its loading and operating temperature. The sensor performance is optimal at Pd loadings of less than 0.2 mol% and operating temperatures of 200-262.5 °C, where acetone conversion is around 50%.

Bi2O3 boosts brightness, biocompatibility and stability of Mn-doped Ba3(VO4)2 as NIR-II contrast agent.

Deep-tissue fluorescence imaging remains a major challenge as there is limited availability of bright biocompatible materials with high photo- and chemical stability. Contrast agents with emission wavelengths above 1000 nm are most favorable for deep tissue imaging, offering deeper penetration and less scattering than those operating at shorter wavelengths. Organic fluorophores suffer from low stability while inorganic nanomaterials (e.g. quantum dots) are based typically on heavy metals raising toxicity concerns. Here, we report scalable flame aerosol synthesis of water-dispersible Ba3(VO4)2 nanoparticles doped with Mn5+ which exhibit a narrow emission band at 1180 nm upon near-infrared excitation. Their co-synthesis with Bi2O3 results in even higher absorption and ten-fold increased emission intensity. The addition of Bi2O3 also improved both chemical stability and cytocompatibility by an order of magnitude enabling imaging deep within tissue. Taken together, these bright particles offer excellent photo-, chemical and colloidal stability in various media with cytocompatibility to HeLa cells superior to existing commercial contrast agents.

Simultaneous Nanothermometry and Deep-Tissue Imaging.

Bright, stable, and biocompatible fluorescent contrast agents operating in the second biological window (1000-1350 nm) are attractive for imaging of deep-lying structures (e.g., tumors) within tissues. Ideally, these contrast agents also provide functional insights, such as information on local temperature. Here, water-dispersible barium phosphate nanoparticles doped with Mn5+ are made by scalable, continuous, and sterile flame aerosol technology and explored as fluorescent contrast agents with temperature-sensitive peak emission in the NIR-II (1190 nm). Detailed assessment of their stability, toxicity with three representative cell lines (HeLa, THP-1, NHDF), and deep-tissue imaging down to about 3 cm are presented. In addition, their high quantum yield (up to 34%) combined with excellent temperature sensitivity paves the way for concurrent deep-tissue imaging and nanothermometry, with biologically well-tolerated nanoparticles.

Single-Nanoparticle Thermometry with a Nanopipette.

Thermal measurements at the nanoscale are key for designing technologies in many areas, including drug delivery systems, photothermal therapies, and nanoscale motion devices. Herein, we present a nanothermometry technique that operates in electrolyte solutions and, therefore, is applicable for many in vitro measurements, capable of measuring and mapping temperature with nanoscale spatial resolution and sensitive to detect temperature changes down to 30 mK with 43 µs temporal resolution. The methodology is based on local measurements of ionic conductivity confined at the tip of a pulled glass capillary, a nanopipettete, with opening diameters as small as 6 nm. When scanned above a specimen, the measured ion flux is converted into temperature using an extensive theoretical support given by numerical and analytical modeling. This allows quantitative thermal measurements with a variety of capillary dimensions and is applicable to a range of substrates. We demonstrate the capabilities of this nanothermometry technique by simultaneous mapping of temperature and topography on sub-micrometer-sized aggregates of thermoplasmonic nanoparticles heated by a laser and observe the formation of micro- and nanobubbles upon plasmonic heating. Furthermore, we perform quantitative thermometry on a single-nanoparticle level, demonstrating that the temperature at an individual nanoheater of 25 nm in diameter can reach an increase of about 3 K.

Silica-Coated TiN Particles for Killing Cancer Cells.

Photothermal therapy (PTT) using plasmonic nanoparticles for cancer treatment is on the verge of clinical application. Titanium nitride (TiN) nanoparticles offer a promising alternative to commonly used gold-based systems at a fraction of the costs. Little is known, however, about the relationship between TiN particle characteristics and their optical properties in colloidal systems. Here, TiN nanoparticles with closely controlled characteristics are prepared by nitridation of TiO2, and their use as PTT agents is explored. Emphasis is placed on the particle surface and core oxygen content, which dominate the TiN optical properties. Colloidal suspensions were studied under UV-vis and near-infrared (NIR) laser irradiation and correlated to particle characteristics. High nitridation temperatures and long residence times lead to increased NIR light absorption. Too high nitridation temperatures, however, lead to particle aggregation that deteriorated their optical properties. This was overcome with SiO2 coating of TiO2 nanoparticles prior to nitridation: the resulting SiO2-coated TiN particles exhibited increased plasmonic performance compared to bare TiN, which is attributed to reduced plasmonic coupling effects. The optimized SiO2-coated TiN had a photothermal efficiency of 58.5% and mass extinction coefficient of 31.6 L g-1 cm-1, outperforming commercial gold nanoshells that are used in clinical trials. The potential of SiO2-coated TiN for photothermal therapy was demonstrated by controllably killing HeLa cells in vitro.

Nd3+-Doped BiVO4 luminescent nanothermometers of high sensitivity.

Neodymium-doped BiVO4 nanoparticles are explored for luminescent nanothermometry in the first and second biological windows. The nanothermometer sensitivity can be increased by an order of magnitude through careful selection of excitation wavelength and emission peaks, leading to sub-degree resolution and penetration depth up to 6 mm in biological tissues.