The present invention provides a zirconia sintered body containing a fluorescent agent and having excellent translucency and excellent strength. The present invention also provides a zirconia shaped body and a zirconia calcined body from which the zirconia sintered body can be obtained. The present invention relates to a zirconia sintered body comprising a fluorescent agent, wherein the zirconia sintered body comprises 4.5 to 9.0 mol % yttria, and has a crystal grain size of 180 nm or less, and a three-point flexural strength of 500 MPa or more. The present invention relates to a zirconia shaped body comprising a fluorescent agent, wherein the zirconia shaped body comprises 4.5 to 9.0 mol % yttria, and has a three-point flexural strength of 500 MPa or more after being sintered at 1,100° C. for 2 hours under ordinary pressure, and a crystal grain size of 180 nm or less after being sintered at 1,100° C. for 2 hours under ordinary pressure. The present invention relates to a zirconia calcined body comprising a fluorescent agent, wherein the zirconia calcined body comprises 4.5 to 9.0 mol % yttria, and has a three-point flexural strength of 500 MPa or more after being sintered at 1,100° C. for 2 hours under ordinary pressure, and a crystal grain size of 180 nm or less after being sintered at 1,100° C. for 2 hours under ordinary pressure.

The present invention provides a zirconia sintered body containing a fluorescent agent and having excellent translucency and excellent strength. The present invention also provides a zirconia shaped body and a zirconia calcined body from which the zirconia sintered body can be obtained. The present invention relates to a zirconia sintered body comprising a fluorescent agent, wherein the zirconia sintered body comprises 4.5 to 9.0 mol % yttria, and has a crystal grain size of 180 nm or less, and a three-point flexural strength of 500 MPa or more. The present invention relates to a zirconia shaped body comprising a fluorescent agent, wherein the zirconia shaped body comprises 4.5 to 9.0 mol % yttria, and has a three-point flexural strength of 500 MPa or more after being sintered at 1,100° C. for 2 hours under ordinary pressure, and a crystal grain size of 180 nm or less after being sintered at 1,100° C. for 2 hours under ordinary pressure. The present invention relates to a zirconia calcined body comprising a fluorescent agent, wherein the zirconia calcined body comprises 4.5 to 9.0 mol % yttria, and has a three-point flexural strength of 500 MPa or more after being sintered at 1,100° C. for 2 hours under ordinary pressure, and a crystal grain size of 180 nm or less after being sintered at 1,100° C. for 2 hours under ordinary pressure.

Self-assembly methods are provided for making hedgehog-shaped microparticles or nanoparticles. The method may comprise combining a metal-containing (e.g., Fe, Au) precursor, a chalcogen-containing precursor (e.g., Se, S), and a self-assembly additive (e.g., dodecanethiol (DT), oleylamine (OLA), hexadecyltrimethylammonium bromide (CTAB)). At least one hedgehog-shaped nanoscale, mesoscale, or microscale particle is formed that defines a core region formed of a first material and a plurality of needles connected to and substantially orthogonal to a surface of the core region. The needles comprise a second material. At least one of the first or the second material comprises iron or gold and optionally selenium or sulfur, for example, iron diselenide (FeSe2). Hedgehog-shaped microparticles or nanoparticles formed from such self-assembly methods are also provided. The semiconductor nature of FeSe2 hedgehog-shaped particles enables their utilization in biomimetic catalysis, drug delivery, optics, and energy storage, by way of non-limiting example.

Self-assembly methods are provided for making hedgehog-shaped microparticles or nanoparticles. The method may comprise combining a metal-containing (e.g., Fe, Au) precursor, a chalcogen-containing precursor (e.g., Se, S), and a self-assembly additive (e.g., dodecanethiol (DT), oleylamine (OLA), hexadecyltrimethylammonium bromide (CTAB)). At least one hedgehog-shaped nanoscale, mesoscale, or microscale particle is formed that defines a core region formed of a first material and a plurality of needles connected to and substantially orthogonal to a surface of the core region. The needles comprise a second material. At least one of the first or the second material comprises iron or gold and optionally selenium or sulfur, for example, iron diselenide (FeSe2). Hedgehog-shaped microparticles or nanoparticles formed from such self-assembly methods are also provided. The semiconductor nature of FeSe2 hedgehog-shaped particles enables their utilization in biomimetic catalysis, drug delivery, optics, and energy storage, by way of non-limiting example.

Embodiments of the present disclosure provide methods of forming solid state dual pore sensors which may be used for biopolymer sequencing and dual pore sensors formed therefrom. In one embodiment, a method of forming a dual pore sensor includes providing a pattern in a surface of a substrate. Generally, the pattern features two fluid reservoirs separated by a divider wall. The method further includes depositing a layer of sacrificial material into the two fluid reservoirs, depositing a membrane layer, patterning two nanopores through the membrane layer, removing the sacrificial material from the two fluid reservoirs, and patterning one or more fluid ports and a common chamber.

Provided is a method of fabricating a micro/nanowire having a nanometer- to micrometer-sized diameter at predetermined positions on an object. The method comprises: preparing a micro/nanopipette having a tip with an inner diameter (d.sub.pt) which is substantially the same as the diameter of the micro/nanowire to be fabricated; filling the micro/nanopipette with a solution containing a micro/nanowire-forming material; bringing the solution into contact with the object through the tip of the micro/nanopipette; and pulling the micro/nanopipette apart from the object at a pulling speed lower than or equal to a predetermined critical pulling speed (v.sub.c) to fabricate a micro/nanowire having substantially the same diameter as the inner diameter of the micro/nanopipette tip (d.sub.pt). The critical pulling speed (v.sub.c) is defined by a maximum limit of the pulling speed at which the micro/nanowire to be fabricated has the same diameter as the inner diameter of the micro/nanopipette tip (d.sub.pt).

Embodiments of the present disclosure provide plasmonic structures, methods of making plasmonic structures, and the like.

An ink includes a solvent, and light-emitting elements dispersed in the solvent, each of the light-emitting elements comprising semiconductor layers and an insulating film partially surrounding outer surfaces of the semiconductor layers, wherein the solvent has Hansen solubility parameters of a polarity parameter between about 4 and about 9 and a hydrogen bonding parameter between about 6 and about 11.

Systems and methods for mechanosynthesis are disclosed, including those that avoid the need for a bootstrap process, avoid the need to build tips via mechanosynthesis, avoid the need for charging tips with feedstock during a build sequence, avoid the need to dispose of reaction byproducts, which reduce the design complexity of new tips, and/or which reduce or avoid the need for multiple positional means and/or tip switching.

3D nanochannel interleaved devices for molecular manipulation are provided. In one aspect, a method of forming a device includes: forming a pattern on a substrate of alternating mandrels and spacers alongside the mandrels; selectively removing the mandrels from a front portion of the pattern forming gaps between the spacers; selectively removing the spacers from a back portion of the pattern forming gaps between the mandrels; filling i) the gaps between the spacers with a conductor to form first electrodes and ii) the gaps between the mandrels with the conductor to form second electrodes; and etching the mandrels and the spacers in a central portion of the pattern to form a channel (e.g., a nanochannel) between the first electrodes and the second electrodes, wherein the first electrodes and the second electrodes are offset from one another across the channel, i.e., interleaved. A device formed by the method is also provided.