Hybrid energy storage device charging
View Patent ↗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 charging a charge storage device, the method comprising
establishing a potential between a cathode and an anode of the charge storage device, the charge storage device including an electrolyte;
receiving a first charge carrier of the electrolyte at a surface effect dominant site of the anode;
transferring an electron of the anode to the first charge carrier;
receiving a second charge carrier of the electrolyte at an intercalation material of the anode; and
transferring an electron from the intercalation material to the second charge carrier.
2. The method of claim 1 , wherein the first charge carrier includes lithium.
3. The method of claim 1 , wherein the potential results in an electrostatic potential difference between the surface effect dominant site and the intercalation material of less than 2.4V.
4. The method of claim 1 , wherein the surface effect dominant site is configured to catalyze intercalation of the first charge carrier into the intercalation material.
5. The method of claim 1 , wherein the surface effect dominant site is disposed on a nanoparticle including titanium.
6. The method of claim 1 , wherein the surface effect dominant site is one of a layer of surface effect dominant sites in a layer on a surface of the intercalation material.
7. The method of claim 1 , wherein the steps of receiving the first charge carrier and receiving the second charge carrier occur contemporaneously.
8. The method of claim 1 , wherein the surface effect dominant site is one of a plurality of surface effect dominant sites distributed within a binder.
9. The method of claim 8 , wherein a concentration of the surface effect dominant sites adjacent to a surface of the intercalation material is greater than a concentration of the surface effect dominant sites elsewhere within the binder.
10. The method of claim 8 , wherein the step of receiving the second charge carrier causes an increase in a volume of the intercalation material and a reduction in a surface density of the surface effect dominant sites on the intercalation material.
11. A method of charging a charge storage device, the method comprising:
establishing a potential gradient at an anode of the charge storage device, the anode including an electrolyte, a plurality of nanoparticles having surface effect dominant sites, an intercalation material and a substrate;
receiving a first charge carrier of the electrolyte at one of the surface effect dominant sites;
transferring an electron to the first charge carrier from the one of the surface effect dominant sites;
receiving a second charge carrier at the intercalation material of the anode; and
transferring an electron from the intercalation material to the second charge carrier.
12. The method of claim 11 , wherein the first charge carrier includes lithium.
13. The method of claim 11 , wherein the second charge carrier is an oxide of the first charge carrier.
14. The method of claim 11 , wherein the surface effect dominant sites are configured to catalyze intercalation of the first charge carrier into the intercalation material.
15. The method of claim 11 , wherein the first charge carrier and the second charge carrier consist of the same chemical species.
16. The method of claim 11 , wherein the intercalation material includes Ag, Al, Bi, C, Ge, Sb, Si, Sn or Zn.
17. The method of claim 11 , wherein the plurality of nanoparticles are disposed on a surface of the intercalation material.
18. The method of claim 11 , wherein the intercalation material is coated on a support filament.
19. The method of claim 11 , wherein the intercalation material is coated on a vertically aligned carbon nanofiber.
20. The method of claim 11 , wherein transferring the electron of the first charge carrier from the one of the surface effect dominant sites occurs at a first reaction potential and transferring the electron to the second charge carrier from the intercalation material occurs at a second reaction potential, the first and second reaction potentials being differently by less than 2.4V.
21. The method of claim 11 , wherein receiving the second charge carrier at the intercalation material results in a decrease in the surface coverage of the nanoparticles on the intercalation material.
22. The method of claim 11 , wherein receiving the second charge carrier at the intercalation material results in an increase in a rate at which charge carriers can be intercalated in the intercalation material.
23. The method of claim 11 , wherein the surface effect dominant sites are configured to produce an oxide of the first charge carrier and the intercalation material is configured to reduce the second charge carrier.
24. The method of claim 11 , further comprising transferring an oxygen from the intercalation material to the surface effect dominant sites.
25. The method of claim 24 , wherein the oxygen is received at the intercalation material from the surface effect dominant sites as an oxide of the first charge carrier.
26. The method of claim 1 , wherein the surface effect dominant site is disposed on one of a plurality of nanoparticles supported by a substrate and wherein the intercalation material is disposed in a layer.
27. The method of claim 11 , further comprising transferring an electron from the intercalation material to the surface effect dominant sites in response to the transferring the electron to the first charge carrier from the one of the surface effect dominant sites.
28. The method of claim 11 , wherein the surface effect dominant sites are configured to adsorb charge carriers in the faradaic interaction.
29. The method of claim 18 , wherein the intercalation material includes silicon and coats less than 25% of the support filament.