Heterojunction

Source: Wikipedia, the free encyclopedia.

A heterojunction is an interface between two

fast ion conductor
and semiconducting materials.

Manufacture and applications

Heterojunction manufacturing generally requires the use of

van der Waals heterostructures.[2]

Despite their expense, heterojunctions have found use in a variety of specialized applications where their unique characteristics are critical:

Energy band alignment

The three types of semiconductor heterojunctions organized by band alignment.
Band diagram for stradding gap, n-n semiconductor heterojunction at equilibrium.

The behaviour of a semiconductor junction depends crucially on the alignment of the

energy bands
at the interface. Semiconductor interfaces can be organized into three types of heterojunctions: straddling gap (type I), staggered gap (type II) or broken gap (type III) as seen in the figure.[8] Away from the junction, the band bending can be computed based on the usual procedure of solving Poisson's equation.

Various models exist to predict the band alignment.

  • The simplest (and least accurate) model is Anderson's rule, which predicts the band alignment based on the properties of vacuum-semiconductor interfaces (in particular the vacuum electron affinity). The main limitation is its neglect of chemical bonding.
  • A common anion rule was proposed which guesses that since the valence band is related to anionic states, materials with the same anions should have very small valence band offsets. This however did not explain the data but is related to the trend that two materials with different anions tend to have larger
    conduction band
    offsets.
  • Tersoff
    AlGaAs
    .
  • The 60:40 rule is a heuristic for the specific case of junctions between the semiconductor GaAs and the alloy semiconductor AlxGa1−xAs. As the x in the AlxGa1−xAs side is varied from 0 to 1, the ratio tends to maintain the value 60/40. For comparison, Anderson's rule predicts for a GaAs/AlAs junction (x=1).[11][12]

The typical method for measuring band offsets is by calculating them from measuring exciton energies in the luminescence spectra.[12]

Effective mass mismatch

When a heterojunction is formed by two different

band structure. In order to calculate the static energy levels within the achieved quantum well, understanding variation or mismatch of the effective mass
across the heterojunction becomes substantial. The quantum well defined in the heterojunction can be treated as a finite well potential with width of . In addition, in 1966, Conley et al. in a quantum well, known as BenDaniel–Duke boundary condition. According to them, the envelope function in a fabricated quantum well must satisfy a boundary condition which states that and are both continuous in interface regions.

Using the Schrödinger equation for a finite well with width of and center at 0, the equation for the achieved quantum well can be written as:

Solution for above equations are well-known, only with different(modified) k and [15]

.

At the z = even-parity solution can be gained from

.

By taking derivative of (5) and multiplying both sides by

.

Dividing (6) by (5), even-parity solution function can be obtained,

.

Similarly, for odd-parity solution,

.

For

numerical solution
, taking derivatives of (7) and (8) gives

even parity:

odd parity:

where .

The difference in effective mass between materials results in a larger difference in ground state energies.

Nanoscale heterojunctions

Image of a nanoscale heterojunction between iron oxide (Fe3O4 — sphere) and cadmium sulfide (CdS — rod) taken with a TEM. This staggered gap (type II) offset junction was synthesized by Hunter McDaniel and Dr. Moonsub Shim at the University of Illinois in Urbana-Champaign in 2007.

In

anisotropic
structures such as the one seen in the image on the right.

It has been shown

conduction bands in these structures is the conduction band offset. By decreasing the size of CdSe nanocrystals grown on TiO2, Robel et al.[17] found that electrons transferred faster from the higher CdSe conduction band into TiO2. In CdSe the quantum size effect is much more pronounced in the conduction band due to the smaller effective mass than in the valence band, and this is the case with most semiconductors. Consequently, engineering the conduction band offset is typically much easier with nanoscale heterojunctions. For staggered (type II) offset nanoscale heterojunctions, photoinduced charge separation can occur since there the lowest energy state for holes may be on one side of the junction whereas the lowest energy for electrons is on the opposite side. It has been suggested[17] that anisotropic staggered gap (type II) nanoscale heterojunctions may be used for photocatalysis, specifically for water splitting
with solar energy.

See also

References

Further reading