Hybrid energy storage device production
A novel hybrid lithium-ion anode material based on coaxially coated Si shells on vertically aligned carbon nanofiber (CNF) arrays. The unique cup-stacking graphitic microstructure makes the bare vertically aligned CNF array an effective Li + intercalation medium. Highly reversible Li + intercalation and extraction were observed at high power rates. More importantly, the highly conductive and mechanically stable CNF core optionally supports a coaxially coated amorphous Si shell which has much higher theoretical specific capacity by forming fully lithiated alloy. Addition of surface effect dominant sites in close proximity to the intercalation medium results in a hybrid device that includes advantages of both batteries and capacitors.
1. A method of producing an energy storage device, the method comprising:
providing a conductive substrate;
growing support filaments on the substrate;
applying intercalation material to the support nanofibers, the intercalation material being configured for intercalation of charge carriers;
applying a plurality of surface effect dominant sites in close proximity to the intercalation material, wherein the surface effect dominant sites are disposed on nanoparticles with a difference in Zeta potentials of the intercalation material and the nanoparticles greater than or equal to 25 mV; and
wherein the nanoparticles form at least a monolayer on surfaces of the intercalation material when the energy storage device is discharged.
2. The method of claim 1 , wherein the support filaments include carbon nanotubes or carbon nanowires.
3. The method of claim 1 , wherein the nanoparticles include titanium.
4. The method of claim 1 , wherein the nanoparticles surface coverage for the intercalation material and the surface coverage of the nanoparticles is reduced by charging the energy storage device.
5. The method of claim 1 , wherein the intercalation material includes silicon particles having an over-layer of silicon oxide.
6. The method of claim 1 , wherein the intercalation material covers less than 25% of the support filaments.
7. The method of claim 1 , wherein the surface effect dominant sites are configured to undergo redox reactions with the charge carriers.
8. The method of claim 1 , wherein the surface effect dominant sites are configured to adsorb charge carriers in a faradaic interaction.
9. The method of claim 1 , wherein the surface effect dominant sites are configured such that faradaic interaction between the charge carriers and surfaces of the nanoparticles dominate faradaic interactions between the charge carriers and the bulk of the nanoparticles.
10. The method of claim 1 , wherein the nanoparticles are less than 34 nanometers in diameter.