Nanoarchitectures for lithium-ion batteries

Some recent work focused on developing materials that are electrochemically active within the range where electrolyte decomposition or electrolyte/electrode reactions do not occur.

[1] A research concept has been proposed in which the major parts of lithium-ion batteries, that is, the anode, electrolyte, and cathode, are combined into one functional molecule.

Thin film two dimensional batteries are restricted to between 2-5 micrometres, limiting areal capacity to significantly less than that of three-dimensional geometries.

The requisite layers, an anode, separator, and cathode, for a battery were then added by low-pressure chemical vapor deposition.

The electrochemically active area consists of 50 nm nanoparticles, smaller than the critical size for crack propagation.

Relative to a two dimensional battery the length (L) over which transport must occur is decreased by two-thirds, which improves kinetics and reduces ohmic loses.

The printer deposited the inks onto the teeth of two gold combs, forming an interlaced stack of anodes and cathodes.

[6] A version of the concentric cylinder packed particles or close-packed polymer to create a three-dimensionally ordered macroporous (3DOM) carbon anode.

3DOM materials have a unique structure of nanometer thick walls that surround interconnected and closed-packed sub-micrometer voids.

[13] Nanowires have been incorporated into the anode/cathode matrix to provide a builtin conductive charge collector and enhancing capacity.

[16] Periodic structures lead to non-uniform current densities that lower efficiency and decrease stability.

Fabrication is through coating the ambigel with a polymer electrolyte and then filling the void space with RuO2 colloids that act as an anode.

As geometries become more complex, non-line-of-sight methods to in-fill the design with electrolyte materials supply the oppositely charged electrode is essential.

However, chemical and physical heterogeneity leaves molecular-level control a significant challenge, especially since the electrochemistry for energy storage is not defect-tolerant.

However, problems exist with the deposition of polymers within complex geometries, e.g. pores, on the size scale of 50-300 nm, resulting in defective coatings.

The precision is because reactions are confined to the surface containing an active chemical moiety that reacts with a precursor; this limits thickness to one monolayer.

This self-limiting growth is essential for complete coatings since deposition does not inhibit the access by other polymeric units to non-coated sites.

Thicker samples can be produced by cycling gases in a similar manner to alternating with oppositely charged polymers in LbL.

In practice ALD may require a few cycles in order to achieve the desired coverage and can result in varied morphologies such as islands, isolated crystallites, or nanoparticles.

The iron was then coatedwith palladium nanoparticles, which effectively reduced carbon's destructive reaction with oxygen and improved the discharge cycle.

As the scale continuous to decrease and transport through the solid becomes more difficult, pre-equilibration is needed to ensure coating uniformity.