In general, the lifetime of a battery is determined by how great of a volume change it undergoes when cycling from the charged to uncharged state and vice versa. Volume changes imply stress and the gradual introduction of defects that can trap electrons and reduce electrical conductivity. For LiFePO4 cathodes, the volume change is around 4-7 %, but this is a crystalline material. Silicon nanowires are amorphous (i.e. poorly ordered) and the introduction of defects on cycling is not necessarily an issue.
The previous work was truly proof of principal, but unlikely for variety of reasons to be a direct path to commercialization. There's some new work out by a local group that expands on the work of Chen. Fleischeur et al. tried their specialty, glancing angle vapour deposition, to form a thin-film of Silicon composed of many, regular pillars. (Disclosure: our research group collaborates with the group that did this research. I personally do not, however.) In glancing angle deposition, the substrate (onto which the film is deposited) is at nearly right angles to the incoming vapour stream. In thin film deposition, one tends to see small clusters form first due to surface tension. As the clusters grow, they amalgamate together and form a (porous) solid thin film. When the substrate is at high angles of incidence, the first clusters to form shadow any smaller trees and grab more than their fair share of the incoming mass stream. Hence glancing-angle deposition typically forms column-like thin films.
The glancing-angle fabrication method has a number of potential advantages over Chan's technique:
- Chan's thin film process relied on a gold catalyst ($$$), whereas the GLAD process only requires a thin layer of chromium for adhesion on Si substrate and none at all on a stainless steel substrate.
- Glancing-angle deposition can easily control the spacing of pillars by patterning the substrate.
- The glancing-angle films were "robust" when I asked the author about it. He said hitting the batteries with a hammer had no effect on performance, so presumably the pillars were not breaking.
- Glancing-angle deposition requires a microscopically smooth surface for proper column formation.
Figure 1: Chan et al. charge capacity after 10 total cycles.
Figure 2: Fleischauer et al. charge capacity after cycling up to cycle 70. I don't recall the reason for the discontinuities but I vaguely recall it had something to do with the test electronics.
Both authors show a very large drop in charge capacity after the first recharge. This means there is some sort of irreversible change to the material occuring from film fabrication to charged and uncharged Si. Then there is a progressive loss in capacity. Evidently Chan and company are less confident in their material as they are only showing results up to ten cycles. Average capacity fade for Fleischeur's battery was found to be 0.3 % per cycle. If we extrapolate, that would imply it would take approximately 750 cycles for the charge capacity of the silicon anode to drop below that of a conventional graphite one. Obviously, that's not good enough for commercial applications.
Overall, I think that this is an important step in terms of fabrication and longevity. We are still looking at a minimum of a decade before any such silicon Li-ion batteries hit the shelves; this is progress on that path.
I completely agree what you said. As well, In order to make battery, we need to place membrane and cathode on the top of the anode and then press it so that we can minimize the volume. the pressure on the anode may destroy the anode wires. the battery that they made may have large volume compare with the weight of anode materials. Since they calculated the capacity based on weight, their data will show 10 times higher than other commercial bateries but the size of battery will be 10 times larger than commercial batteries.
In other hand, if they want to prove that their battery has excellent cyclability, they should show at least 500cycles. otherwise, their tech may be useless in battery industries.
Post a Comment