General Remarks
Optoelectronics, as well as practically all other devices made from compound semiconductors, always contain heterojunctions, i.e. junctions between two different semiconductors, for a variety of reasons.  
One possible reason was already mentioned: Transparency to light generated in some active part.  
But there are many other advantages so compelling that extremely complicated heterostructures are now routinely produced despite a lot of problems that are encountered, too.  
Below the conduction band structure of an advanced Al_{x}Ga_{1x}As device is shown to illustrate that point. The doping is shown in brackets; "i" means undoped (= intrinsic). SQW is short for "Single Quantum Well"  whatever that may be.  
There are many heterojunctions and we will not be able to delve very deep into the subject. The logic behind this structure will be made clear in a later chapter.  

In this subchapter we will look at some major properties of heterojunctions. First of all: How do we construct a band diagram?  
Lets first look at the basic cases that we may encounter when considering heterojunctions. Naturally, the bandgaps are always different, but only specifying E_{g}(1) and E_{g}(2) (and of course the Fermi energy in (1) and (2)) is not sufficient to describe the heterosystem before the contact of the materials (1) and (2)  
We also must specify the exact position on the energy scale of one of the band edges. This then gives rise to three distinct cases for heterojunctions as illustrated below together with the necessary definitions of the various energies needed.  
You may want to consult a special modul (in German) dealing with some of the questions that may come up.  


Looking at the left hand (Type I) case, we first discuss the various energies encountered:  
In contrast to "simple" band diagrams in Si, the vacuum energy level is now included (and defines the zero point of the energy axis). We also have the energy of the band edges, E_{C} and E_{V}, and from their difference the bandgap energy E_{g}.  
By convention, the difference between the
conduction band edge and the vacuum energy is defined as a potential called
"electron affinity
c"; q · c is thus the work needed to move a charge from the
(lower) conduction band edge to infinity. 

Note that this is not exactly the same as the electron affinity in more chemical oriented lingo, where it is the energy gained by the reaction X + e ^{–} = X^{ } and thus only defined by atoms that form stable negatively charged ions..  
The difference between the Fermi energy and the vacuum energy is given by charge times the workfunction Q of the material, q · Q is thus the energy needed to move a fictitious electron (because in semiconductors usually there is none at the Fermi energy) from the Fermi energy to infinity.  
Note that while c is a material constant, Q is not  it changes with the position of the Fermi energy.  
We may also define the differences of the band edges between the two materials, D E_{C} and D E_{V}, although they are implicitely given by the prime material parameters c and E_{G} = E_{C} – E_{C}.  
The three types of heterojunctions possible are:  
Type I : (straddling) The bandgap of one semiconductor is completely contained in the bandgap of the other one; i.e. E_{C}(2) > E_{V}(1) and E_{V}(2) < E_{V}(1). The discontinuities of the bands are such that both types of carriers, electrons and holes, need energy (D E_{C} and D E_{V}, resp.) to change from the material with the smaller band gap to the one with the larger gap  the carriers from the other side gain this energy. Type I heterojunctions are quite common, the important GaAs  AlGaAs system belongs to this kind.  
Type II: (staggered) The bandgaps overlap, but one D E_{C/V} changes sign. The situation with respect to moving carriers from (1) to (2) or vice verse is no longer symmetrical. One kind of carrier gains energy (in the example if electrons move from right to left), the other one needs energy (the holes). The InP/InSb system provides an example  
Type III (brokengap): The bandgaps do not overlap at all. The situation for carrier transfer is like type II, just more pronounced. The system GaSb/InAs belongs to this type.  
Construction of Band Diagrams  
What happens if we join the two materials? Exactly the same thing as for differently doped Si:  
Carriers will flow across the junction, building space charges (and now possibly also interface charges) until the Fermi energy is the same everywhere in the material. Far away from the junction, everything is unchanged.  
However, there are pronounced differences to the case of a pnjunction in Si. Lets imagine symmetrical junctions, i.e. the majority carrier concentration is identical in the p and npart. For homojunctions, the number of electrons flowing into the ptype part is then the same as the number of electrons flowing into the npart. However, at least in the type I case, only one kind of carrier will flow as is obvious and shown below. The space charge regions to the left and right of the junction thus might not be symmetric.  


Still, some kind of carrier transfer will happen and the electrostatic potential far away from the junction will rise from a constant level on one side to a different, but constant level on the other side. The difference will be equal to the difference in Fermi energy before the contact divided by the elementary charge. To the left and the right of the junction the bands are bend accordingly, and so is the vacuum energy.  
Lets see how far this recipe takes us with a simple GaAs  AlGaAs type I junction  


First, we align the Fermi energies. Then we bend the bands  in a smaller region on the more heavily doped side  but always identical for the band edges! After all, the vacuum potential at some position x is fixed and so are the band edges relative to the vacuum potential.  
This leaves us with something new: We can not join the two materials! If we adjust the band bending on both sides so that the conduction bands match, the valence band won't match and vice verse. We must introduce a discontinuity right at the interface at one of the bands or at both.  
The next picture shows how to do that for type I heterojunctions for both possible doping cases.  


Some kind of cusp or notch must form in the conduction or valence band, depending on the details of the system. Exactly what happens and what the cusps look like depends on many details, you must solve the Poisson equation properly for a specific case.  
Again, a discontinuity like this must happen, even at "ideal" interfaces. We don't know exactly what it looks like, but we can now take this potential and plug it into a onedimensional Poisson equations and see what it means for the charge distribution.  
Unavoidably, there must be a dipole layer right at the interface (look at this basic module if you have problems figuring that out). The distance between the charges of this dipole layer is so small, however (atomic size) that it does not influence the carrier movement (there is an acceleration/deacceleration process with equal magnitudes at a very small scale in classical terms or effortless tunneling in quantummechanical terms).  
This dipole layer with its sharp wiggle in the charge distribution is therefore usually not included in drawings of the heterojunction.  
In reality, the matching of two lattice types with different atoms on both sides may well introduce some interface states in the bandgap, as discussed for the free Si surface.  
Depending on the Fermi level (which is of course influenced by the interface states, too), these interface states may be charged and introduce some band bending of their own.  
To make things even more complicated (for pessimists), or to add more possibilities for engineering with heterojunction (for optimists), we now can produce junctions with specific properties between materials of the same doping type  even for identical carrier concentrations.  
This type of heterojunction is sometimes called an isotype junction, the pntype a diode type junctions. Other people use abbreviations, e.g. with upper case letters indicating the doping type of the material with the wider bandgap, and lower case letters the other one. We than have Pn, pN, Np, and nP junctions of the diode type, and Nn, nN, Pp, and pP junctions of the isotype. If we look ahead, we can now easily denote multijunctions like PnP, and so on.  
Isotype junctions must also have band discontinuities at the interface, the next picture shows examples.  


You may already wonder what properties to expect from this kind of junction and what it is good for; we will discuss that later.  
We now have a degree of freedom for all heterojunctions, which did not occur for homojunctions: How do we distribute the discontinuity?  
In the left hand diagrams above, e.g., we could decrease DE_{C} and increase D E_{V} by an identical amount, making the cusp more pronounced; or we do it the other way around. How can we find the real case?  
The answer is: Nobody knows how to do that in some kind of comprehensive theory. The simplest model (called the Anderson model) assumes that D E_{C} is equal to the difference in the electron affinities c  


But that is only a rough estimate that may be quite wrong (not to mention that bulk electron affinities can not be calculated with any precision and measurements always obtain the (different) surface electron affinities).  
There is, however, one feature of the discontinuities that makes life somewhat easier: Whatever its value, it is determined by the interaction of the atoms at the interface and interatomic forces are responsible for its value.  
This simply means that its value does not change much if we change properties of the materials on a scale much larger than the atomic scale. In other words:  
The band bending necessary for adjusting the potentials on both sides of the junction so that the Fermi energy is identical, may be seen as independent of the value of the discontinuities. If we construct a band diagram, we simply always keep the same value for the discontinuities, no matter what else we do with the bands.  
Properties of Heterojunctions  
How do we measure the values of the discontinuities? The answer is: Make the heterojunction and measure the junction properties.  
In order to do that, we need to know how the discontinuities influence measurable quantities. How, for example, does the precise nature of the discontinuities influence the current  voltage characteristics across a heterojunction? Or, if there is some radiative recombination, the quantum or current efficiencies?  
We are now entering deep water. Or are we? After all, the equations for IVcharacteristics across a junction (without the space charge layer part) in the simple or more complex form did not contain anything about the shape of the band bending  only the potential difference and bulk properties of materials to the left and right of the junction.  
This tells us, that the basic diode characteristics (assuming that nothing happens in the space charge region) must still be valid in its general form, but with one big difference that transfers into a decisive property of heterojunctions:  
The hole and electron part of the total current now are different even for a perfectly symmetric junction!  
This is most easily seen if we look at the relation between the two partial currents j_{e} and j_{h}, which we called the injection ratio k = j_{e}/ j_{h}. Taking the values from the simple diode equation given before, we obtain  


Rewriting this equation in terms of the carrier mobilities, and the doping concentration (assuming fully ionized dopants) with the relations given before, we obtain  


For homojunctions, the intrinsic carrier concentration n_{i} is the same on both sides, but not for heterojunctions! For the intrinsic carrier concentrations of any semiconductor we have the basic equations:  


With E_{Fi} = Fermi energy for the intrinsic case.  
Only for the case that N ^{e}_{eff} = N ^{h}_{eff} would the Fermi energy be in the middle of the band gap; and while we always used that approximation for Si, we must be more careful with compound semiconductors.  
But independent of the exact position of the Fermi energy, we always have  


Inserting this relation into the equation for the injection ratio k from above, introducing the difference of the band gaps of material 1 and material 2 as DE_{g} = E_{g}(1) – E_{g}(2), and substituting "1" and "2" for "nside" and "pside" because this relation is valid for any heterojunction of the diode type, we obtain for k  


This is a very important equation for optoelectronics. Lets see why:  
If DE_{g} is sufficiently large  and since it is in an exponential term, it does not have to be very large  it will always overwhelm the possible asymmetries in the preexponential term, e.g. because of different doping levels, or effective density of states between the two materials, and this means k is very different from 1. Getting all signs right, we have the following situation  


In other words: In heterojunctions of the diode type, injection of the majority carriers from the material with the larger band gap (almost) always far surpasses the reverse process.  
To give a relevant example: For a GaAs/Ga_{0,7}Al_{0,3}As junction with DE_{g} = 0,3 eV and for doping concentrations of 10^{18} cm^{–3} or 2 · 10^{17} cm^{–3}, respectively, we have k » 10^{6}.  
Why is a large value of k so important?  
Because if we sandwich a small gap semiconductor between two large gap semiconductors, we should be able to inject a lot of electrons from one side and a lot of holes from the other side with no means of escape. The injected carriers must recombine in the small gap part which is our recombination zone  we have a large current efficiency h_{cu}.  
If you think about that a minute and try to come up with some structure, you will realize, that there is a problem: You can not have injection via two pnjunctions  one junction must be an isotype junction. But luckily, isotype junctions have similar properties: it is easy to inject majority carriers from the wide band gap side and not so easy from the other side. 
© H. Föll (Semiconductor  Script)