Semiconduction devices having a thin film structure...

Active solid-state devices (e.g. – transistors – solid-state diode – Non-single crystal – or recrystallized – semiconductor... – Amorphous semiconductor material

Reexamination Certificate

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C257S059000, C257S064000, C438S096000, C438S097000

Reexamination Certificate

active

06239451

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates generally to the production of semiconductor thin film materials, and more particularly to ultra-thin film highly conductive materials used as a contact layer in photovoltaic cells, p-i-n detectors, radiation sensors and the like.
BACKGROUND OF THE INVENTION
Thin film, p-type and n-type highly conductive materials are used as contact layers in many semiconductor structures, including photovoltaic cells, particle detectors, X-ray and electromagnetic radiation detectors that convert incoming radiation to electrical output signals.
As shown in
FIG. 1
, such devices
2
typically include a layer of semiconductor detecting material
4
that detects the incoming particle or electromagnetic radiation
6
, and emits an electrical signal
8
in response to such detection. A front (or radiation entry) surface of the detecting material is at least partially covered by a layer of thin film, preferably high conductivity material
10
to which a first electrical lead
12
is coupled. Commonly, device
2
includes a thin layer of protective transparent substrate material such as glass
14
that overlies this contact layer
10
. A back surface of material
4
is at least partially covered by a layer of high conductivity material
16
to which a second electrical lead
18
is coupled. In some devices, the lower surface of back contact layer
16
is made reflective
20
to cause incoming radiation to pass through the detection layer twice, effectively increasing the device signal output. In such applications, back contact layer
16
must be thin so as not to attenuate incoming radiation enroute to the reflective region
20
. Electrical contact between the device
2
and the outside world is via contact layers
10
and
16
using leads
12
and
18
. The present invention is directed toward the production of an improved thin film material suitable for front contact layer
10
and, where a thin layer is required, for back contact layer
16
.
Incoming radiation
6
(e.g., light, IR, X-ray, etc.) must pass at least partially through front contact layer
10
(as well as the transparent layer
14
) before entering the detection layer. Therefore, to reduce attenuation, the front contact layer's thickness
22
should be minimal, preferably 200 Å or less for photovoltaic cells, and 800 Å or less for electromagnetic radiation detectors. Further, because electrical signals from the device
2
must pass through the upper contact layer before reaching lead
12
, layer
10
should be highly conductive electrically, to minimize signal loss. Because electrical signals also pass through lower contact surface
16
before reaching lead
18
, layer
16
should also be highly conductive electrically to minimize electrical losses. However layer
16
need not be thin unless a reflective surface
20
is utilized by the device
2
.
It has been surprisingly difficult in the prior art to produce highly conductive deposited thin film material for use in semiconductors. In the prior art, contact layer materials are either a heavily doped amorphous material, or a heavily doped microcrystalline semiconductor material. Semiconductor devices including such materials are not optimally designed because the radiated losses and contact layer resistance are excessive. As a result, such devices tend to be inefficient and require a relatively large amount of incoming radiation to produce a useful electrical output signal.
The prior art's use of amorphous material for contact layers, for example as the p-layer and/or n-layer in a p-i-n structure, has drawbacks because by nature amorphous materials store energy that can dissipate over time. During dissipation, the energy promotes chemical reactions that create instability and degradation in any semiconductor material using the material.
In addition, it is well known that light can cause degradation in amorphous silicon materials, and thus amorphous photovoltaic devices experience conversion efficiency degradation relatively rapidly. Further, semiconductor dopants tend not to modulate conductivity as efficiently in amorphous materials as in crystalline structures, which results in more resistive contact layers.
The other prior art approach to manufacturing a thin film contact layer avoids amorphous materials, and instead uses a fine-grained microcrystalline material, such as the material depicted for layer
10
in FIG.
1
. Using this approach, the crystals are created during a deposition growth (e.g., plasma enhanced chemical vapor deposition). Post-deposition, the crystals may be subjected to an annealing process to increase the grain size and improve electrical conductivity. Often, however, annealing cannot be accomplished because the temperatures required to increase grain size (and thus improve electrical conductivity) exceed about 950° C. Frequently such high temperatures cannot be tolerated by the other materials in the device, e.g., the substrate, the detector layer. For example, prior art detectors on inexpensive glass substrates do not employ such annealed contact layers because of the excessive heat that would be required.
Large grain size, where it can be achieved in contact layers, would promote improved conductivity by minimizing the number of grain boundaries, which tend to “soak up” semiconductor dopants and carriers, rendering them less effective and making the contact layer material less conductive. Generally a large grain size is associated with a large volume fraction of the crystalline material.
Unfortunately prior art deposition-created crystals are essentially isotropic microcrystals, growing during deposition no larger laterally than the film thickness. Thus as depicted schematically in
FIG. 1
, contact layer
10
comprises a layer of many small sized microcrystals
24
, whose lateral dimensions are no larger than the contact layer's thickness
22
. Further, because the crystals
24
have such small grain size, there are many grain boundaries
26
that absorb dopant as well as carriers, hindering electrical conductivity. Although larger microcrystals
24
could be grown by increasing the film thickness
22
, thereby improving electrical conductivity by decreasing the number of grain boundaries
26
, the increased thickness would degrade optical transmission due to increased absorption losses. Although for ease of illustration, the crystals
24
are depicted as identical cubes in
FIG. 1
, in reality the essentially isotropic crystals need not necessarily be identical in size and shape to one another.
Generally, such deposition produced microcrystalline silicon contact layers (doped p-type or doped n-type) have conductivities in the range of 10
−3
to 10 S/cm, but only for thicknesses exceeding 800 Å. As film thickness is decreased below about 400 Å, conductivity falls by many orders of magnitude. This conductivity loss coincides with a decrease in Raman signal strength at 520cm
−1
, which corresponds to the volume fraction of Si in the crystalline phase, and coincides with an increase in the Raman signal at 480 cm
−1
, which corresponds to volume fraction of Si in the amorphous phase.
In summary, there is a need for an ultra-thin contact material that is highly conductive electrically. Preferably such material should be stable, easily doped and highly responsive to doping, and capable of production using a low temperature semiconductor process. The present invention discloses such a material, and a low temperature method for producing the material.
SUMMARY OF THE INVENTION
The present invention discloses a process for minimizing grain boundaries in an ultra-thin polycrystalline material, thereby lessening absorption of dopants and carriers into such boundaries and thus substantially improving the material's electrical conductivity. The resultant ultra-thin highly conductive material is especially suitable for use as a semiconductor contact layer.
In the prior art, isotropic crystals are grown during deposition and, in situations where high process

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