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Lanthanide-doped glasses and crystals are attractive for laser applications because the metastable energy levels of the trivalent lanthanide ions facilitate the establishment of population inversion and amplified stimulated emission at relatively low pump power. At the nanometre scale, lanthanide-doped upconversion nanoparticles (UCNPs) can now be made with precisely controlled phase, dimension and doping level. When excited in the near-infrared, these UCNPs emit stable, bright visible luminescence at a variety of selectable wavelengths, with single-nanoparticle sensitivity, which makes them suitable for advanced luminescence microscopy applications. Here we show that UCNPs doped with high concentrations of thulium ions (Tm), excited at a wavelength of 980 nanometres, can readily establish a population inversion on their intermediate metastable H level: the reduced inter-emitter distance at high Tm doping concentration leads to intense cross-relaxation, inducing a photon-avalanche-like effect that rapidly populates the metastable H level, resulting in population inversion relative to the H ground level within a single nanoparticle. As a result, illumination by a laser at 808 nanometres, matching the upconversion band of the H → H transition, can trigger amplified stimulated emission to discharge the H intermediate level, so that the upconversion pathway to generate blue luminescence can be optically inhibited. We harness these properties to realize low-power super-resolution stimulated emission depletion (STED) microscopy and achieve nanometre-scale optical resolution (nanoscopy), imaging single UCNPs; the resolution is 28 nanometres, that is, 1/36th of the wavelength. These engineered nanocrystals offer saturation intensity two orders of magnitude lower than those of fluorescent probes currently employed in stimulated emission depletion microscopy, suggesting a new way of alleviating the square-root law that typically limits the resolution that can be practically achieved by such techniques.

The ultimate frontier in nanomaterials engineering is to realize their composition control with atomic scale precision to enable fabrication of nanoparticles with desirable size, shape and surface properties. Such control becomes even more useful when growing hybrid nanocrystals designed to integrate multiple functionalities. Here we report achieving such degree of control in a family of rare-earth-doped nanomaterials. We experimentally verify the co-existence and different roles of oleate anions (OA−) and molecules (OAH) in the crystal formation. We identify that the control over the ratio of OA− to OAH can be used to directionally inhibit, promote or etch the crystallographic facets of the nanoparticles. This control enables selective grafting of shells with complex morphologies grown over nanocrystal cores, thus allowing the fabrication of a diverse library of monodisperse sub-50 nm nanoparticles. With such programmable additive and subtractive engineering a variety of three-dimensional shapes can be implemented using a bottom–up scalable approach.

Each single upconversion nanocrystal (UCNC) usually contains thousands of photon sensitizers and hundreds of photon activators to up-convert near-infrared photons into visible and ultraviolet emissions. Though in principle further increasing the sensitizers' concentration will enhance the absorption efficiency to produce brighter nanocrystals, typically 20% of Yb ions has been used to avoid the so-called "concentration quenching" effect. Here we report that the concentration quenching effect does not limit the sensitizer concentration and NaYbF is the most bright host matrix. Surface quenching and the large size of NaYbF nanocrystals are the only factors limiting this optimal concentration. Therefore, we further designed sandwich nanostructures of NaYbF between a small template core to allow an epitaxial growth of the size-tunable NaYbF shell enclosed by an inert shell to minimize surface quenching. As a result, the suspension containing 25.2 nm sandwich structure UCNCs is 1.85 times brighter than the homogeneously doped ones, and the brightness of each single 25.2 nm heterogeneous UCNC is enhanced by nearly 3 times compared to the NaYF: 20% Yb, 4% Tm UCNCs in similar sizes. Particularly, the blue emission intensities of the UCNCs with the sandwich structure in the size of 13.6 and 25.2 nm are 1.36 times and 3.78 times higher than that of the monolithic UCNCs in the similar sizes. Maximizing the sensitizer concentration will accelerate the development of brighter and smaller UCNCs as more efficient biomolecule probes or photon energy converters.

We propose and demonstrate a thinned fiber based Mach-Zehnder interferometer for multi-purpose sensing applications. The sensor head is formed by all-fiber in-line singlemode-multimode-thinned-singlemode (SMTS) fiber structure, only using the splicing method. The principle of operation relies on the effect that the thinned fiber cladding modes interference with the core mode by employing a multimode fiber as a mode coupler. Experimental results showed that the liquid refractive index information can be simultaneously provided from measuring the sensitivity of the liquid level. A 9.00 mm long thinned fiber sensor at a wavelength of 1538.7228 nm exhibits a water level sensitivity of -175.8 pm/mm, and refractive index sensitivity as high as -1868.42 (pm/mm)/RIU, respectively. The measuring method is novel, for the first time to our knowledge. In addition, it also demonstrates that by monitoring the wavelength shift, the sensor at a wavelength of 1566.4785 nm exhibits a refractive index sensitivity of -25.2935 nm/RIU, temperature sensitivity of 0.0615 nm/°C, and axial strain sensitivity of -2.99 pm/με, respectively. Moreover, the sensor fabrication process is very simple and cost effective.

A positive margin results in a significantly worse outcome for pT1-2, pN0-1, and I-II stage gastric cancer patients who undergo D2/D3 lymphadenectomy, but not for those in pT3-4, pN2-3, and III-IV stage.

The rN stage has more potential advantages in minimizing stage migration phenomenon for patients with insufficient number or level of lymph nodes retrieved.

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