Additives for self-standing electrodes
A method of making a self-supportive electrode material that includes providing an aerosolized plurality of carbon nanotubes in a carbon nanotube synthesis reactor, transporting the aerosolized plurality of carbon nanotubes directly from the carbon nanotube synthesis reactor to a mixing chamber, contacting the aerosolized plurality of carbon nanotubes in the mixing chamber with an aerosolized electrode active material from a first chamber to provide a substantially homogenous aerosol mixture of the carbon nanotubes and the electrode active material, and depositing the carbon nanotubes and the electrode active material on a substrate to provide a self-supportive electrode material. Also described are systems for performing the disclosed method and self-supportive electrode materials provided by the method.
1. A method of making a self-supportive electrode material, the method comprising:
providing an aerosolized plurality of carbon nanotubes in a carbon nanotube synthesis reactor;
transporting the aerosolized plurality of carbon nanotubes directly from the carbon nanotube synthesis reactor to a mixing chamber;
providing an aerosol mixture by contacting the aerosolized plurality of carbon nanotubes in the mixing chamber with an aerosolized electrode active material from a first chamber and an aerosolized additive from a second chamber;
creating a vortex of the aerosol mixture in the mixing chamber to provide a substantially homogenous aerosol mixture comprising the carbon nanotubes, the electrode active material, and the additive; and
depositing the carbon nanotubes, the electrode active material, and the additive directly on a porous substrate to provide a self-supportive electrode material.
2. The method of claim 1 , wherein the aerosolized electrode active material is provided in a vortex in the first chamber.
3. The method of claim 2 , wherein the first chamber comprises an inlet configured to provide a flow of carrier gas sequentially through a porous frit and a bed of the electrode active material in a first direction.
4. The method of claim 3 , wherein the first chamber further comprises one or more tangential inlets configured to provide one or more tangential flows of carrier gas in a direction that is tangential to the first direction.
5. The method of claim 3 , wherein the first chamber comprises a shaker configured to agitate the bed of the electrode active material in the first direction.
6. The method of claim 1 , wherein the aerosolized additive is provided in a vortex in the second chamber.
7. The method of claim 6 , wherein the second chamber comprise an inlet configured to provide a flow of carrier gas sequentially through a porous frit and a bed of the additive in a first direction.
8. The method of claim 7 , wherein the second chamber further comprises one or more tangential inlets configured to provide one or more tangential flows of carrier gas in a direction that is tangential to the first direction.
9. The method of claim 1 , wherein the electrode active material comprises a lithium metal oxide, a lithium iron phosphate, or a combination thereof.
10. The method of claim 1 , wherein the electrode active material comprises graphite.
11. The method of claim 1 , wherein the porous substrate is movable.
12. The method of claim 1 , wherein the self-supportive electrode material comprises the carbon nanotubes at a concentration of between about 0.01 and 10% w/w of a concentration of the electrode active material.
13. The method according to claim 12 , wherein the self-supportive electrode material comprises the carbon nanotubes at a concentration of about 1% w/w of the concentration of the electrode active material.
14. The method according to claim 1 , wherein the aerosolized plurality of carbon nanotubes and the aerosolized electrode active material are provided to the mixing chamber at a combined flow rate of between about 0.5 to 2.5 L/min.
15. The method of claim 1 , wherein the additive comprises graphene flakes.
16. The method of claim 1 , further comprising pressing the self-supportive electrode active material to a density of between about 0.1 and 3 g/cm 3 .