The invention relates to a host material for stabilizing a Li metal electrode, fabricating methods and applications of the same. The host material includes crumpled graphene balls operably defining a scaffold having volumes and voids inside and in between the crumpled graphene balls so as to allow uniform and stable Li deposition/dissolution inside and in between the crumpled graphene balls without electrode volume fluctuations or with sufficiently small electrode volume fluctuations. The crumpled paper ball-like structures of graphene particles can readily assemble to yield the scaffold with scalable Li loading up to 10 mAh cm-2 within tolerable volume fluctuations. High Coulombic efficiency of 97.5% over 750 cycles (1500 hours) is achieved. Plating/stripping Li up to 12 mAh cm-2 on the crumpled graphene scaffold does not experience dendrite growth.

Embodiments of the present disclosure describe methods of preparing hollow silica nanoparticles comprising one or more of the following steps: contacting a polymer and a first solvent to obtain a first solution in which the polymer is dissolved; contacting the first solution and a second solvent to obtain a second solution in which a polymer template is formed by precipitation; contacting a silica precursor and the second solution to obtain a shell-core structure in which a silica shell is formed around the polymer template; contacting the shell-core structure with a third solvent to remove the polymer template from the shell-core structure; and recovering one or more of hollow silica nanoparticles, the polymer, and the polymer template.

The disclosure extends to biodegradable hollow nanoparticles, and systems, methods, devices, and processes for producing the same. The disclosure includes a method of preparing a hollow mesoporous nanoparticle by providing a plurality of silica core particles. Each of the plurality of silica core particles comprises a diameter within a range of about 600 nanometers to about 30 nanometers. The method further includes synthesizing a mesoporous silica shell around the plurality of silica core particles forming a plurality of mesoporous coated silica core particles. Further, the method provides for etching the plurality of mesoporous coated silica core particles with an aqueous solution of sodium carbonate and water to remove the silica core particle from the plurality of mesoporous coated silica core particles forming a plurality of hollow mesoporous particles. The method also includes diffusing a payload into the plurality of hollow mesoporous particles in an aqueous solution.

A cathode material, a preparation method thereof, a lithium ion battery and a vehicle are provided. The cathode material comprises elemental sulfur and secondary particles formed by packing primary particles, wherein the secondary particles have a hollow structure, and the elemental sulfur fills in gaps among the primary particles and in the hollow structure. The primary particles comprise a lithium oxide, wherein the lithium oxide comprises δLiNi.sub.mCo.sub.nX.sub.(1-m-n)O.sub.2.Math.(1−δ)Li.sub.2MO.sub.3, 0≤δ≤1, X comprises at least one selected from Mn, Al, Nb, and Fe, M comprises at least one of Mn, Al, Nb, Fe, Co, and Ni, 0≤m<1, 0≤n<1, and 0≤m+n<1.

The present invention relates to methods of fabrication of hollow shells/spheres/particles, core-shell particles and composite materials made from these particles.

Certain embodiments of the invention provide TiO.sub.2 nanoshell particles, methods of fabricating TiO.sub.2 nanoshell particles, and methods of enriching peptides in a sample using TiO.sub.2 nanoshell particles.

A method for forming hollow silica spheres by dissolving a hydrolyzable aryl silane in an aqueous solution of water and an acid to form a hydrolyzed silane solution, mixing the hydrolyzed silane solution with a hydroxide base to form a precipitate, and calcining the precipitate in a multi-stage calcination procedure that includes (a) heating to a first temperature of 180 to 240° C. with a first ramp rate of 3 to 10° C./min and holding the first temperature for 2 minutes to 2 hours, then (b) heating to a second temperature of 600 to 740° C. at a second ramp rate of 0.1 to 4° C./min, and holding the second temperature for 2 to 24 hours.

Embodiments described herein generally relate to compositions including discrete nanostructures (e.g., nanostructures including a functionalized graphene layer and a core species bound to the functionalized graphene layer), and related articles and methods. A composition may have a coefficient of friction of less than or equal to 0.02. Discrete nanostructures may have a substantially non-planar configuration. A core species may reversibly covalently bind a first portion of a functionalized graphene layer to a second portion of the functionalized graphene layer. Articles, e.g., articles including a plurality of discrete nanostructures and a means for depositing the plurality of discrete nanostructures on a surface, are also provided. Methods (e.g., methods of forming a layer) are also provided, including depositing a composition onto a substrate surface and/or applying a mechanical force to the composition, e.g., such that the composition exhibits a coefficient of friction of less than or equal to 0.02.

Provided are a cathode active material having a suitable particle size and high uniformity, and a nickel composite hydroxide as a precursor of the cathode active material. When obtaining nickel composite hydroxide by a crystallization reaction, nucleation is performed by controlling a nucleation aqueous solution that includes a metal compound, which includes nickel, and an ammonium ion donor so that the pH value at a standard solution temperature of 25° C. becomes 12.0 to 14.0, after which, particles are grown by controlling a particle growth aqueous solution that includes the formed nuclei so that the pH value at a standard solution temperature of 25° C. becomes 10.5 to 12.0, and so that the pH value is lower than the pH value during nucleation. The crystallization reaction is performed in a non-oxidizing atmosphere at least in a range after the processing time exceeds at least 40% of the total time of the particle growth process from the start of the particle growth process where the oxygen concentration is 1 volume % or less, and with controlling an agitation power requirement per unit volume into a range of 0.5 kW/m.sup.3 to 4 kW/m.sup.3 at least during the nucleation process.

The present invention discloses the morphology of hollow, double-shelled submicrometer particles generated through a rapid aerosol-based process. The inner shell is an essentially hydrophobic carbon layer of nanoscale dimension (5-20 nm), and the outer shell is a hydrophilic silica layer of approximately 5-40 nm, with the shell thickness being a function of the particle size. The particles are synthesized by exploiting concepts of salt bridging to lock in a surfactant (CTAB) and carbon precursors together with iron species in the interior of a droplet. This deliberate negation of surfactant templating allows a silica shell to form extremely rapidly, sealing in the organic species in the particle interior. Subsequent pyrolysis results in a buildup of internal pressure, forcing carbonaceous species against the silica wall to form an inner shell of carbon. The incorporation of magnetic iron oxide into the shells opens up applications in external stimuli-responsive nanomaterials.