Processes for forming metal oxide thin films on electrode interphase control
This invention provides a novel solution to form an artificial interphase on the electrode to protect it from fast declining electrochemical behaviors, by depositing Metal Oxides Layer, by ALD or CVD. Metals discussed here are IVA-VIA elements (Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W). The film needs to be thin, possibly discontinuous, and lithium ion conductive enough, so that the addition of this thin film interface allows fast lithium ion transfer at the interface between electrode and electrolyte.
1 . A method of coating a cathode or a cathode active material with a metal oxide film, the method comprising the steps of:
a1. exposing the cathode or cathode active material to a chemical precursor vapor comprising a precursor of the formula M(═NR a )(OR b ) 2 (NR 2 2 ) and an oxygen source as an oxidizing co-reactant, and
b1. depositing the metal oxide film on the cathode or cathode active material,
wherein:
M is selected from Nb, Ta, or V,
R a is selected from iPr, tBu, t-Am
R b each is independently selected from Et, iPr, tBu, sBu or SPen, and
R c each is independently selected from Et or Me.
2 . The method of claim 1 , wherein the precursor is of the formula M(═NR a )(OR b ) 2 (NMeEt).
3 . The method of claim 2 , further comprising a step of purging the chemical precursor vapor prior to step of exposing the cathode or cathode active material to a co-reactant.
4 . The method of claim 1 , wherein for R b at least one is independently selected from sBu or SPen.
5 . The method of claim 4 , wherein both R b are independently selected from sBu or SPen.
6 . The method of claim 4 , wherein the step b1. depositing the metal oxide film on the cathode or cathode active material comprises an atomic layer deposition step.
7 . The method of claim 4 , wherein the step b1. of depositing the metal oxide film on the cathode or cathode active material comprises a chemical vapor deposition step.
8 . The method of claim 1 , wherein the precursor is of the formula M(=NR a )(OR b ) 2 (NMeEt) and wherein for R b at least one is independently selected from sBu or SPen.
9 . The method of claim 1 , wherein the precursor is Nb(═NtBu)(NEt 2 )(O-tBu) 2 , Nb(═NtBu)(NEt 2 ) 2 (O-tBu), Ta(═NtBu)(NEt 2 )(O-tBu) 2 , Ta(═NtBu)(NEt 2 ) 2 (O-tBu), and mixtures thereof.
10 . The method of claim 1 , wherein the step of exposing the cathode or cathode active material to a chemical precursor vapor and the step of exposing the cathode or cathode active material to a co-reactant, are sequentially performed.
11 . The method of claim 1 , wherein the co-reactant is an oxygen source; an oxygen-containing silicon precursor, an oxygen-containing tin precursor, a phosphate, diethyl phosphoramidate, or a sulfate.
12 . The method of claim 1 , wherein the metal oxide film produced by step b1. has an average atomic composition of Nb x O y D z , O is oxygen, and D is any other atom(s), and wherein x=0.3-0.4, y=0.4-0.65 and z=0.01-0.1.
13 . The method of claim 1 , wherein a temperature of the chemical precursor vapor and/or the cathode or cathode active material is from 125 degrees C. to 275 degrees C.
14 . The method of claim 12 , wherein the metal oxide film has an average thickness of 0.02 nm to 10 nm.
15 . The method of claim 1 , wherein the cathode active material, or the cathode active material in the cathode, is selected from the group consisting of a) layered oxides; b) spinel cathode materials; c) Olivine structured cathode materials,; and combinations thereof.
16 . The method of claim 1 , wherein one or more of steps a1. and b1. are performed from one to ten times.
17 . The method of claim 16 , wherein a) the temperature of the chemical precursor vapor and/or the cathode or cathode active material is from 100 degrees C. to 300 degrees C.; b) the metal oxide film has an average thickness of 0.02 nm to 10 nm; and c) the metal oxide film is at least 50% continuous on a surface of the cathode or cathode active material.