Active electrode material
The invention relates to active electrode materials and to methods for the manufacture of active electrode materials. Such materials are of interest as active electrode materials in lithium-ion or sodium-ion batteries. The invention provides a method of making an active electrode material, the method comprising: providing a mixed niobium oxide; combining the mixed niobium oxide with a carbon precursor to form an intermediate material, wherein the carbon precursor comprises polyaromatic sp 2 carbon and is selected from pitch carbons, graphene oxide, and mixtures thereof; and heating the intermediate material under reducing conditions to pyrolyse the carbon precursor forming a carbon coating on the mixed niobium oxide and introducing oxygen vacancies into the mixed niobium oxide, thereby forming the active electrode material.
1 . A method of making an active electrode material, the method comprising:
providing a mixed niobium oxide having a Wadsley-Roth or Tetragonal Tungsten Bronze crystal structure, wherein the mixed niobium oxide is expressed by the formula MNb b O c , wherein M represents one or more cations, b satisfies 0.13≤b≤49, and c satisfies 3.3≤c≤124;
combining the mixed niobium oxide with a carbon precursor to form an intermediate material, wherein the carbon precursor comprises polyaromatic sp 2 carbon and is selected from pitch carbons wherein the intermediate material comprises the carbon precursor in an amount of 0.1-25 wt %; and
heating the intermediate material under reducing conditions to pyrolyse the carbon precursor forming a carbon coating on the mixed niobium oxide and introducing oxygen vacancies into the mixed niobium oxide, thereby forming the active electrode material;
wherein the step of heating the intermediate material under reducing conditions is performed at a temperature in the range of 400-1,200° C. under an inert gas; or under a mixture of an inert gas and hydrogen; or under vacuum; and
wherein the active electrode material has an Ip/IG ratio as observed by Raman spectroscopy within the range of 0.90-1.15.
2 . The method of claim 1 , wherein the pitch carbons are selected from coal tar pitch, petroleum pitch, mesophase pitch, wood tar pitch, isotropic pitch, bitumen, and mixtures thereof.
3 . The method of claim 1 , wherein the intermediate material comprises the carbon precursor in an amount of 0.1-15 wt %, or 0.2-8 wt %, based on the total weight of the mixed niobium oxide and the carbon precursor.
4 . The method of claim 1 , wherein the carbon coating on the active electrode material is present in an amount of up to 10 wt %, or 0.05-5 wt %, or 0.1-3 wt %, based on the total weight of the active electrode material.
5 . The method of claim 1 , wherein the step of combining the mixed niobium oxide with the carbon precursor comprises high energy milling.
6 . The method of claim 1 , wherein the step of combining the mixed niobium oxide with the carbon precursor comprises mixing the mixed niobium oxide with the carbon precursor in a solvent.
7 . The method of claim 1 , wherein the step of heating the intermediate material under reducing conditions is performed at a temperature in the range of 500-1,100° C. or 600-900° C.
8 . The method of claim 1 , wherein the step of heating the intermediate material under reducing conditions is performed for a duration within the range of 30 minutes to 12 hours, or 1-9 hours, or 2-6 hours.
9 . The method of claim 1 , wherein the step of heating the intermediate material under reducing conditions is performed under an inert gas.
10 . The method of claim 1 , comprising
providing the mixed niobium oxide;
heating the mixed niobium oxide under reducing conditions to introduce oxygen vacancies into the mixed niobium oxide, thereby forming an oxygen-deficient mixed niobium oxide;
combining the oxygen-deficient mixed niobium oxide with the carbon precursor comprising polyaromatic sp 2 carbon to form the intermediate material; and
heating the intermediate material under reducing conditions to pyrolyse the carbon precursor forming a carbon coating on the oxygen-deficient mixed niobium oxide and introducing further oxygen vacancies into the oxygen-deficient mixed niobium oxide, thereby forming the active electrode material.
11 . The method of claim 1 , wherein the carbon coating is semi-crystalline.
12 . The method of claim 11 , wherein the carbon coating provides a peak in an XRD pattern of the active electrode material centred at 2θ of about 26° with a width (full width at half maximum) of at least 0.20°, or at least 0.25°, or at least 0.30°.
13 . The method of claim 1 , wherein the active electrode material has an ID/IG ratio as observed by Raman spectroscopy within the range of 0.90-1.10, or 0.95-1.05.
14 . The method of claim 1 , wherein the mixed niobium oxide is expressed by the formula [M1] x [M2] (1-x) [Nb] y [O] z , wherein:
M1 and M2 are different;
M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, Sb, Y, La, Hf, Ta, Re, Zn, In, or Cd;
M2 represents one or more of Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, Sb, Y, La, Hf, Ta, Re, Zn, In, or Cd; and wherein
x satisfies 0<x<0.5;
y satisfies 0.5≤y≤49; and
z satisfies 4≤z≤124.
15 . The method of claim 14 , wherein
(i) M2 represents one or more of Mo, W, V, Zr, Al, Ga, Ge, Zn, Ta, Cr, Cu, K, Mg, Ni, Hf; or
(ii) M2 represents one or more of Mo, W, V, Zr, Al, Ga, Ge, Zn, Ta, Cu, K, Mg; or
(iii) M2 represents one or more of Mo, W, V, or Zr.
16 . The method of claim 14 , wherein
(i) M1 represents one or more of K, Mg, Ca, Y, Ti, Zr, Hf, V, Ta, Cr, Mo, W, Mn, Fe, Co, Ni, Cu, Zn, Al, Ga, Si, Ge, Sn, Sb; or
(ii) M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Cu, Ga, Ge, K, Ni, Al, Hf, Ta, or Zn; or
(iii) M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Ga, Ge, Al, or Zn.
17 . The method of claim 14 , wherein
(i) x satisfies 0.01≤x≤0.4; and/or
(ii) x satisfies 0.05≤x≤0.25; and/or
(iii) x is about 0.05.
18 . The method of claim 1 , wherein the mixed niobium oxide is expressed by the formula [M1] x [M2] (1-x) [Nb] y [O] z , wherein:
M1 and M2 are different;
M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, Sb, Y, La, Hf, Ta, Re, Zn, In, or Cd;
M2 represents one or more of Mg, V, Cr, W, Zr, Mo, Cu, Ga, Ge, Ca, K, Ni, Co, P, Al, Sn, Mn, Ce, Sb, Y, La, Hf, Ta, Zn, In, or Cd; and wherein
x satisfies 0<x<0.5;
y satisfies 0.5≤y≤49; and
z satisfies 4≤z≤124.
19 . The method of claim 1 , wherein the mixed niobium oxide has the formula M1 x Mo (1-x) Nb 12 O (33-33 α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, or Sb; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05.
20 . The method of claim 1 , wherein the mixed niobium oxide has the formula M1 x W (1-x) Nb 0.57 O (4.43-4.43 α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, or Sb; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05.
21 . The method of claim 1 , wherein the mixed niobium oxide has the formula M1 x Zn (1-x) Nb 17 O (43.5-43.5 α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, or Sb; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05.
22 . The method of claim 1 , wherein the mixed niobium oxide has the formula M1 x Al (1-x) Nb11O (29-29 α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, or Sb; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05.
23 . The method of claim 1 , wherein the crystal structure of the mixed niobium oxide does not correspond to the crystal structure of TiNb 2 O 7 .
24 . The method of claim 1 , wherein the active electrode material is in particulate form, wherein the active electrode material has a D50 particle diameter in the range of 0.1 100 μm, or 0.5-50 μm, or 1-15 μm.
25 . The method of claim 1 , wherein the active electrode material has a BET surface area in the range of 0.1-100 m 2 /g, or 0.5-50 m 2 /g, or 1-20 m 2 /g.
26 . The method of claim 1 , wherein the mixed niobium oxide is expressed by the formula [M1] x [M2] (1-x) [Nb] y [O] z :
M1 and M2 are different;
M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, K, Ni, Al, Ta, or Zn;
M2 represents one or more of Mg, V, Cr, W, Zr, Nb, Mo, Cu, Fe, Ga, Ge, Zn, Ca, K, Ni, Al, Mn, Hf or Ta; and wherein
x satisfies 0<x<0.5;
y satisfies 0.5≤y≤49; and
z satisfies 4≤z≤124.
27 . The method of claim 1 , wherein the mixed niobium oxide is expressed by the formula [M1] x [M2] (1-x) [Nb] y [O] z , wherein:
M1 and M2 are different;
M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Cu, Ga, Ge, K, Ni, Al, Hf, Ta, or Zn;
M2 represents one or more of Mo, W, V, Zr, Al, Ga, Ge, Zn, Ta, Cu, K, or Mg; and wherein
x satisfies 0<x<0.5;
y satisfies 0.5≤y≤49; and
z satisfies 4≤z≤124;
wherein the intermediate material comprises the carbon precursor in an amount of 0.2-8 wt %, based on the total weight of the mixed niobium oxide and the carbon precursor; and
wherein the carbon coating on the active electrode material is present in an amount of 0.1-3 wt %, based on the total weight of the active electrode material.
28 . The method of claim 1 , wherein the mixed niobium oxide has the formula:
(i) M1 x Mo (1-x) Nb 12 O (33-33α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Ga, Ge, Al, or Zn; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05; or
(ii) M1 x W (1-x) Nb 0.57 O (4.43-4.43α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Ga, Ge, Al, or Zn; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05; or
(iii) M1 x Zn (1-x) Nb 17 O (43.5-43.5α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Ga, Ge, Al, or Zn; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05; or
(iv) M1 x Al (1-x) Nb 11 O (29-29α) where M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Ga, Ge, Al, or Zn; and wherein x satisfies 0<x<0.5; and α satisfies 0≤α≤0.05; and
wherein the intermediate material comprises the carbon precursor in an amount of 0.2-8 wt %, based on the total weight of the mixed niobium oxide and the carbon precursor;
wherein the carbon coating on the active electrode material is present in an amount of 0.1-3 wt %, based on the total weight of the active electrode material;
wherein the carbon precursor is petroleum pitch.
29 . The method of claim 1 , wherein the carbon precursor is petroleum pitch.
30 . A method of making an electrode, comprising making an active electrode material by following the method of claim 1 , and forming an electrode comprising the active electrode material in electrical contact with a current collector.