Bi-Metallic Rare Earth Oxide Nanomaterials

Abstract

Disclosed are nanomaterials that are comprised of R.sub.xO.sub.yM.sup.1M.sup.2 clusters, where R is one or more lanthanides selected from La, Ce, Pr, Nd, Pm, Sm Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb or Lu, wherein O is oxygen and where M.sup.1 and M.sup.2 are metallic components selected from Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, or Cd, or a metal oxide of the foregoing transition metals.

Claims

1. A nanomaterial comprised of R.sub.xO.sub.yM.sup.1M.sup.2, where R is one or more lanthanides selected from La, Ce, Pr, Nd, Pm, Sm Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb or Lu, wherein O is oxygen and where M.sup.1 and M.sup.2 are metallic components selected from Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, or Cd, or a metal oxide thereof, wherein x is 1-3 and y is 1-3.

2. The nanomaterial of claim 1, wherein M.sup.1 and M.sup.2 comprise different metals, or alternatively, M.sup.1 is a metal and M.sup.2 is a metal oxide of M.sup.1.

3. The nanomaterial of claim 1, wherein the M.sup.1M.sup.2 content is about 2% to about 20%, molar percent of the nanomaterial.

4. The nanomaterial of any of claims 1-4, wherein the nanomaterial comprises particles having a particle size of the range of from 1 nm to 100 nm or from 5 nm to 100 nm or from 5 nm to 25 nm.

5. The nanomaterial of claim 4, wherein the particles are spherical, rod-shaped, star-shaped, or polygonal.

6. The nanomaterial of claim 5, wherein the particles are spherical.

7. The nanomaterial of claim 6, wherein the particles comprise an average diameter of about 50 nm across their largest diameter and are comprised of unique particle phases with average diameters less than 30 nm.

8. The nanomaterial of any of claims 1-7, wherein the particles comprise a lanthanide oxide core with an external surface, wherein the external surface comprises different constituents in different valence states.

9. The nanomaterial of claim 8, wherein M.sup.1 and M.sup.2 comprise a valence state selected from 0, +2, +3, or +4, or a combination thereof, where the valence state of M.sup.1 and M.sup.2 is the same or different, and wherein R comprises a valence state selected from +3, +4, or a combination thereof.

10. The nanomaterial of claim 9, wherein R comprises a mixed valence state with a ratio of R (3+):R (4+) percentages, wherein the ratio is about 80%: 20% to about 20%: 80%, about 75%: 25% to about 25%: 75%, about 60%: 40% to about 25%: 75%, or about 57%: 43% to about 27%: 73%.

11. The nanomaterial of claim 10, wherein the percentage of R (3+) relative to R (4+) is >50% R (3+). In a specific embodiment, R is Ce.

12. A method of producing R.sub.xO.sub.yM.sup.1M.sup.2 nanoparticles, the method comprising dissolving a lanthanide salt (e.g. Ce(NO3)3) in water to form a lanthanide solution at a concentration of 5 mM to about 50 mM; dissolving a first metal salt in water and a second metal salt in water at concentrations up to 20 mol % for each metal component, optionally the first metal salt and second metal salt being dissolved in the same or different solutions; hydrolyzing the lanthanide to form lanthanide oxide; and mixing the first metal and second metal salt solution(s) with the lanthanide solution during the hydrolyzing step to form a lanthanide/metal mixture; and aging lanthanide/metal mixture to form R.sub.xO.sub.yM.sup.1M.sup.2 nanoparticles, where R is one or more lanthanides selected from La, Ce, Pr, Nd, Pm, Sm Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb or Lu, wherein O is oxygen and where M.sup.1 and M.sup.2 are metallic components selected from Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, or Cd, or a metal oxide thereof, wherein x is 1-3 and y is 1-3.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0004] FIG. 1: Transmission Electron Microscopy images of Bi-Metallic Nano rare Earth Oxide particle (77WC) formulations. Nano rare Earth Oxide particle (77WC) formulations. A representative formulation was synthesized and is noted here as formulation (1). Particles are largely crystalline, as evidenced by observable lattice fringes. These fringes, along with variation in relative crystallite sizes, suggest formation of the bi-metallic surface phases. Additional formulations may further be synthesized, in fixed nominal compositions, by dissimilar wet chemical syntheses. Differences in particle character among representative formulations will confer the ability to tune a given bi-metallic nano rare earth oxide composition's physicochemical character through modification of synthesis approach. Designed changes to these characters may then be considered for varied, specific applications.

[0005] FIG. 2: Chemical state analysis of bi-metallic nanomaterials. X-ray photoelectron spectroscopy (XPS) measurements (FIG. 2A, survey scan over a relevant binding energy region) with binding energy regions for Ce3d (FIG. 2B), Ag3d (FIG. 2C), and Zn2p (FIG. 2D) chemical states. Peak fittings to Ce.sup.3+ and Ce.sup.4+ states provide insight into the density of oxygen vacancies at the material surface and thereby their unique redox chemistry. Integration of the peak areas demonstrates that the majority of (near-) surface cerium sites are in the reduced state: suggesting a substantial density of surface vacancy sites at which catalytic redox reactions may occur. Interestingly, silver (FIG. 2C) content in the nanoparticle formulation is observed in a metallic state while zinc (FIG. 2D) occurs in both metallic and oxide states. The presence of multiple metal elements (cerium, silver, zinc) in mixed valence states (0, +2, +3, +4) further suggests complex bond structures and interfaces or doping among the varied material components. The range of component valencies may also contribute to observed antimicrobial activates via associated redox reactions such as the generation of free radicals by engineered nanoceria formulations.

DETAILED DESCRIPTION

Overview

[0006] Multi-metal clustering of nano-rare earth oxide (RO, where R is varied from La, Ce to Lu) particles, which initiates complex electron transfer can enable many catalytic reactions. This leads to fast redox active nanoparticles for modulating reactive oxygen species. Combination of various bi-metallic combinations includes transition group of elements from Sc to Cd (2 to 20 at %) (example: CuZn/RO, ZnCd/RO, etc). The chosen bi-metallic components will have limited solid solubility in the nano-rare earth oxide component and will tend to localize towards the rare earth oxide surface at lower bi-metallic component concentrations. When the bi-metallic component concentrations are greater, surface phases may be comparable in size to the rare earth oxide component. The bi-metallic component of the material will participate in fast redox reactions through function as binding sites for chemical substrates and/or mediators of electron transfer within a given chemical reaction. This multi-metal clustering creates more asymmetric oxygen vacancies in host nano-rare earth oxide lattices promotes faster electron transport. This leads to superior catalytic performance for biomedical applications.

Definitions

[0007] Unless specifically stated or obvious from context, as used herein, the term about is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About can be understood as within 30%, 25%, 20%, 15%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from context, all numerical values provided herein are modified by the term about.

DESCRIPTION OF EXEMPLARY EMBODIMENTS

[0008] According to certain embodiments, provided are nanomaterials that are comprised of R.sub.xO.sub.yM.sup.1M.sup.2 clusters, where R is one or more lanthanides selected from La, Ce, Pr, Nd, Pm, Sm Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb or Lu, wherein O is oxygen and where M.sup.1 and M.sup.2 are metallic components selected from Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, or Cd, or a metal oxide of the foregoing transition metals. M.sup.1 and M.sup.2 typically comprise different metals, or alternatively, M.sup.1 might be a metal and M.sup.2 a metal oxide of the same metal of M.sup.1 (e.g., M.sup.1 is zinc and M.sup.2 is zinc oxide). Moreover, M.sup.1 and/or M.sup.2 may include a metal and a metal oxide of the same metal. In a certain embodiment, the M.sup.1M.sup.2 content is about 2% to about 20%, molar percent of the nanomaterial. X may be 1-3 and y may be 1-3. In an embodiment, nanomaterials comprise nanoparticles having a particle size of the range of from 1 nm to 100 nm or from 5 nm to 100 nm or from 5 nm to 25 nm.

[0009] The R.sub.xO.sub.yM.sup.1M.sup.2 nanomaterial are particles, where the particles may be spherical, rod-shaped, star-shaped, or polygonal. In a preferred embodiment, the particles are spherically-shaped, meaning that they more or less approximate the shape of a sphere. Preferably, the average diameter of the spherically-shaped particles is about 20-70 nm. In a certain embodiment, the spherically-shaped lanthanide oxide nanoparticles have an average diameter of 30 nm to 50 nm as measured by transmission electron microscopy. In embodiments in which the particles are not spherically shaped, it is preferred that the average dimension between two opposing sides of the nanoparticles is 50 nm or less.

[0010] The R.sub.xO.sub.yM.sup.1M.sup.2 nanoparticles will have a lanthanide oxide core with an external surface. The surface is characterized by having different constituents in different valence states, i.e., mixed valence states. For example, M.sup.1 and M.sup.2 may comprises a valence state selected from 0, +2, +3, or +4, or a combination thereof, where the valence state of M.sup.1 and M.sup.2 is the same or different. Similarly, R may comprise a valence state selected from +3, +4, or a combination thereof. Although the amount is not intended to be limiting, when used in methods of the invention, some preferred ranges of R (3+):R (4+) percentages are: about 80%: 20% to about 20%: 80%, about 75%: 25% to about 25%: 75%, about 60%: 40% to about 25%: 75%, or about 57%: 43% to about 27%: 73%. In certain embodiments, the percentage of R (3+) relative to R (4+) is >50% R (3+). In a specific embodiment, R is Ce.

[0011] According to another embodiment, provided is a method of producing R.sub.xO.sub.yM.sup.1M.sup.2 nanoparticles. The method involves dissolving a lanthanide salt (e.g. Ce(NO3)3) in water to form a lanthanide solution at a concentration of 5 mM to about 50 mM; dissolving a first metal salt in water and a second metal salt in water at concentrations up to 20 mol % for each metal component (the first metal salt and second metal salt may be dissolved in the same or different solutions); hydrolyzing the lanthanide to form lanthanide oxide; and mixing the first metal and second metal salt solution(s) with the lanthanide solution during the hydrolyzing step to form a lanthanide/metal mixture; and aging lanthanide/metal mixture to form R.sub.xO.sub.yM.sup.1M.sup.2 nanoparticles. Aging involves storing the mixture for a period of time to allow for formation of the nanoparticles, and may also involve subjecting the mixture to an oxidizing agent known in the art.

EXAMPLES

Example 1: Production of Bi-Metal Cerium Oxide Particles

[0012] Synthesis Procedure. A cerium precursor salt, such as Ce(NO.sub.3).sub.3, is dissolved in de-ionized water to a final concentration of 5 to 50 mM. Additional metal (e.g., silver, zinc, zirconium) salts are similarly dissolved to various concentrations, up to 20 mol %, for each component, in de-ionized water and combined with the dissolved cerium salt. The aqueous cerium ion components are then allowed to undergo hydrolysis at elevated or autogenic pH. Hydrolysis and consequent metal oxide particle formation may be accelerated through addition of an oxidizing agent such as hydrogen peroxide (e.g., at a final concentration of at least (0.1 v/v %). Additional metal component, ts are incorporated with the forming cerium oxide phase as dopants and surface phases. Choice of additional metal components, based on respective solubilities in the cerium oxide parent material, allows control over doping versus non-doping, or surface segregating, behaviors. Additionally, choice of pairs of additional metal species will allow control of particle electrochemical properties through band or work function tuning (e.g., choice of metal species based on their individual standard electrochemical positions). The choice of metal species may also allow efficient chemical transformations, such as for catalytic ZnPd intermetallic structures at zinc support surfaces or Ru/Pd structures, with each species contributing to the catalytic pathway. Particles may be aged, in situ or with application of some physicochemical process such as heating, following addition of all reaction components to allow equilibration of particle phase compositions (e.g., decomposition of surface adsorbed peroxide species).

[0013] Those skilled in the art will appreciate that other lanthanide precursor salts and metal salts can be substituted for the cerium precursor salt described in the above example.

Example 2

[0014] As shown in FIG. 1, a representative formulation was synthesized and is noted here as formulation (1), with the nominal molar proportions of metal components as Zn:Ag:Ce->1:1:10. The formulation was analyzed using Transmission Electron Microscopy. Particles are largely crystalline, as evidenced by observable lattice fringes. These fringes, along with variation in relative crystallite sizes, suggest formation of the bi-metallic surface phases. Additional formulations may further be synthesized, in fixed nominal compositions, by dissimilar wet chemical syntheses. Differences in particle character among representative formulations will confer the ability to tune a given bi-metallic nano rare earth oxide composition's physicochemical character through modification of synthesis approach. Designed changes to these characters may then be considered for varied, specific applications.

Example 3

[0015] As shown in FIG. 2, X-ray photoelectron spectroscopy (XPS) measurements were taken (A, survey scan over a relevant binding energy region) with binding energy regions for Ce3d (B), Ag3d (C), and Zn2p (D) chemical states. Peak fittings to Ce.sup.3+ and Ce.sup.4+ states provide insight into the density of oxygen vacancies at the material surface and thereby their unique redox chemistry. Integration of the peak areas demonstrates that the majority of (near-) surface cerium sites are in the reduced state: suggesting a substantial density of surface vacancy sites at which catalytic redox reactions may occur. Interestingly, silver (C) content in the nanoparticle formulation is observed in a metallic state while zinc (D) occurs in both metallic and oxide states. The presence of multiple metal elements (cerium, silver, zinc) in mixed valence states (0, +2, +3, +4) further suggests complex bond structures and interfaces or doping among the varied material components. The range of component valencies may also contribute to observed antimicrobial activates via associated redox reactions such as the generation of free radicals by engineered nanoceria formulations.