The Technology
Solar modules: a variety of technologies
Photovoltaics uses the internal photoelectric effect to generate electricity from sunlight. Incoming light which is absorbed by a semiconductor crystal releases electrons from their bonding state. An electric field is then required to conduct them away from the solid state.
Solar cells have an n-type layer which can emit electrons (emitter) and a p-type layer which can absorb electrons (base). At the boundary interface between the two layers (p-n junction) an electric field is formed, which separates the light-generated charge carriers. A voltage corresponding to the electric field is produced at the terminal contacts of the cell, meaning that current is able to flow as soon as the contacts are connected to each other.
Many types of solar cell have already been developed in laboratories to increase efficiency and reduce costs. Five of these are used commercially today and play a role in the market. The fundamental difference between them is the semiconductor material used and their crystal structure (crystalline or amorphous).
Silicon is the prevailing semiconductor in photovoltaics. Monocrystalline (mono-Si) and multicrystalline (mc-Si) are mainly used. Crystalline silicon solar cells achieve the highest efficiency, however, the manufacture of high-purity silicon requires relatively large amounts of energy and brings with it high costs. Thin-film technology, which requires significantly less material, is therefore used in an endeavor to avoid both of these drawbacks. The following materials are chiefly considered to be suitable semiconductors:
- amorphous silicon (a-Si) and microcrystalline silicon (µc-Si)
- copper indium diselenide (CIS)
- cadmium telluride (CdTe)
First generation photovoltaics technology is based on crystalline silicon. The second generation is based on thin-film technology and the third generation encompasses new technologies which have not yet reached a commercial stage – mainly organic solar cells.
Crystalline silicon cells
A crystalline silicon solar cell consists of a mono- or multicrystalline silicon chip (wafer) approximately 180 mm thick. In order to increase its conductivity, the crystal structure is doped, i.e. foreign atoms are added to the material in a targeted manner. The p-type layer is created by doping the structure with boron; the n-type layer is created by doping it with phosphorus. Metallic, strip-like contacts on the front and rear of the cell draw off the light-generated charge carriers.
Monocrystalline cells have a perfectly regular crystal structure. Multicrystalline cells are made of silicon crystals with grain sizes measuring just a few millimeters. The grain boundaries represent crystal defects to which charge carriers can be bound (recombination). Their efficiency is therefore somewhat lower.
Monocrystalline silicon cells achieve an efficiency of 17 to 18 percent in commercial manufacturing; multicrystalline silicon cells achieve 16 to 17 percent. Special technologies have also been developed to increase efficiency. The following three are the best known of the commercially available technologies:
Buried contacts: Applying contacts to the upper cell surface in the form of metal fingers and busbars reduces the absorptive area. This can be avoided by cutting grooves into the cell using a laser, to create a path for the metal conductors.
Back contact cells: Another way of removing the metal conductors from the upper surface is to place them on the rear side of the cell. The solar cells which currently achieve the highest efficiencies were created using this method.
Heterojunction with Intrinsic Thin Layer (HIT): The HIT cell consists of a thin, single-crystal wafer which is covered on the front and rear with an ultra-thin layer of amorphous silicon. Using both crystalline and amorphous silicon layers increases the cell’s efficiency.
These technologies can increase the efficiency of a crystalline solar cell by over 20 percent.
Thin-film modules
Thin-film modules are photovoltaic modules with an active photoelectric layer only a few micrometers thick, which is deposited using large-area, thin-film technology. The deposition methods employed are mainly those commonly used to coat architectural glass and VDUs. The production units are at least one meter square in size and surpass the area of a silicon solar cell by some two orders of magnitude.
These extremely thin layers are not self-supporting, and consequently need to be mounted on a substrate. Glass is generally used for this purpose, although flexible plastic films are also employed, allowing roll-to-roll coating which offers advantages in terms of production.
Thin-film modules are less efficient than those made with crystalline cells, but this is offset by the following advantages:
- the energy payback time is relatively short due to the low amounts of material and energy consumed
- the manufacturing process can be automated for large-area modules
- a high degree of vertical integration can be achieved, with only a few production steps necessary
- flexible substrates open up new areas of use for the product and its integration into buildings
The most important advantage is that fully-developed production, which allows large production volumes and efficiency to match, brings such major cost benefits that crystalline technology can be equaled or even bettered. This means that a kWh of solar power can be generated at a lower cost. Three technologies have already made the transition to mass production and are enjoying commercial success:
Silicon based thin-film modules are generally made from amorphous silicon (a-Si). Since amorphous silicon can absorb light considerably better than crystalline silicon, a film thickness of about 1 µm is sufficient. However, this material generates fewer charge carriers so the efficiency is substantially lower, lying between four and eight percent. Thin-film modules made from amorphous silicon can be manufactured to very large dimensions (the maximum as at June 2011 is 5.7 m2).
In order to increase the efficiency of an a-Si module, microcrystalline silicon (µc-Si) is added to the amorphous silicon, thereby producing a tandem or micromorph solar cell. The µc-Si layer absorbs more light in the red and infrared parts of the spectrum, and the efficiency increases to ten percent.
Copper-indium-selenium is the active semiconductor material in a CIS module, and is often alloyed with gallium to produce a CIGS module. Sulfur can also be used as an alloying agent to increase efficiency. CIS and CIGS modules have the highest efficiencies of all thin-film modules; an efficiency of 20 percent has already been reached in laboratory conditions, and commercial modules have efficiencies of between seven and twelve percent. The crystal structure of these chalcopyrite compounds corresponds to that of silicon, with the lattice sites occupied by elements of different valences (monovalent copper, trivalent indium, and hexavalent selenium). The outstanding characteristic of these semiconductors is their high tolerance of crystal defects and impurities, as these can combine to form electrically-neutral complexes. Consequently, the demands placed on the raw materials and processes are lower than for other semiconductor materials, resulting in greater scope for savings. The most recent research has shown that, in principle, it is possible to replace indium, a particularly costly element, with zinc.
Cadmium telluride (CdTe) modules are characterized by a relatively high efficiency (eleven percent) combined with low production costs, and are already being manufactured in very high quantities at reasonable cost. Currently, this is the most economic thin-film technology. Use of the heavy-metal cadmium poses particularly high expectations on module recycling, however.
Organic solar cells
The steadily growing demand for photovoltaic modules means that more cost-effective production processes are becoming increasingly necessary. In view of this, the use of organic semiconductors represents a promising approach as they can be processed into large-area, thin layers on flexible films using simple print and film coating methods or vacuum sublimation.
Organic solar cells use a process to generate electricity that works in a similar fashion to the way in which photosynthesis converts the radiant energy from sunlight into chemical energy. This mechanism can be exploited using a suitable combination of strongly absorbing chromophores (semiconducting organic molecules or polymers may be considered) as donors and strong electron acceptors (e.g. fullerenes) for the photovoltaic generation of charge carriers. A layer thickness of around just 0.1 µm is required for the incident light to be completely absorbed.
Organic solar cells produced in the laboratory can reach an efficiency of eight percent. It has been possible to increase their service life to some 5,000 hours, but this is still far too short. Improvements achieved thus far have concentrated above all on the packaging of the cells and less on extending the photoactive materials’ service life.
It will be necessary to synthesize new donor and acceptor materials if organic solar cells are to be further improved. These must firstly be capable of self-organization (as this is crucial for the resulting coatings to be highly ordered) and secondly offer as broad an absorption spectrum as possible, so as to be able to better utilize the sunlight. Hence there is still great potential for increasing photocurrent.
Dye-sensitized cells
A photoelectrochemical reaction ensures the flow of current in dye-sensitized cells. The reaction proceeds in an aqueous environment between a photosensitive dye, which provides the electrons, and electrolytes and a semiconductor material, which transport the charge. While theoretically very inexpensive owing to low material costs, dye-sensitized cells have hitherto suffered from difficulties encountered in sealing the modules. Efficiencies of up to eleven percent have been achieved in laboratories.
Multijunction cells
Multijunction or stacked cells make the best possible use of the solar spectrum. In multijunction cells, alloys of semiconductors with varying band gap energies are layered on top of one another. The band gap energy indicates the wave length until which a semiconductor can absorb light and convert it into electricity. While solar cells with just one semiconductor material reach a theoretical efficiency of 33 percent, the theoretical maximum for solar cells using two semiconductors with different band gaps is 42 percent.
Multijunction or stacked cells are generally made of elements of the third and fifth group of the periodic table. Elements of the third main group are indium (In), gallium (Ga) and aluminum (Al), while arsenic (As), phosphor (P), nitrogen (N) and antimony (Sb) belong to the fifth main group. The compound semiconductors are separated onto monocrystalline germanium wafers, where the germanium is the solar cell with the lowest band gap.
As the production of stacked cells is very complex and expensive, generally only small cells (100 square millimeters) are produced for use in concentrator systems with up to 700-fold concentration.
Concentrator systems use optical lenses to bundle sunlight onto small multijunction cells. These installations generally use tracking systems to follow the sun over the course of the day for optimum yields. The lenses are made of glass or plastic.
Thanks to their heat resistance and their favorable output-to-weight ratio, stacked cells are also used for satellites.
From cell to grid
In a module, solar cells are connected to form an electric unit. Under standard conditions, commercial solar modules achieve an output of between 60 and 360 W. At 25 to 50 V, open-circuit voltage is considerably below grid voltage.
When a string is created by series-connecting several modules, the open-circuit voltage rises. By connecting several strings in parallel, almost any voltage can be achieved.
The direct current supplied by this PV generator is converted into alternating current at grid voltage and frequency by one or several inverters. If required, this conversion can occur with a specified phase shift, in order to feed reactive power into the grid (e.g. in the event of grid failure) and lend it support. Thanks to state-of-the-art power electronics, converting direct current to alternating current now only incurs minimal losses.
The inverter is connected directly to the public grid and must therefore perform several tasks simultaneously. It constantly searches for the maximum power point (MPP) of the PV generator, and records and saves the operational data necessary for monitoring the PV installation’s efficiency. It also displays error messages and sends them to a computer when required. Furthermore, the inverter monitors the grid connection and checks if this has failed or been switched off.
As a result of converting the direct current, losses are incurred which can be relatively high within the partial load range of the inverter (zero to 20 percent of the rated power), but which are usually less than five percent at the rated output. Inverters usually achieve maximum efficiency at around half the rated output; some even reach over 98 percent.
Microgrids and smart grids
The decentralized feed-in of solar power opens up the possibility of creating microgrids from several neighboring PV installations. Using intelligent control engineering, a variable, virtual, large-scale power station can be developed in conjunction with decentralized suppliers and consumers of electricity. As elements in this power plant, the PV installations would contribute to increasing the quantity of decentralized power consumed, thus decreasing the amount of electricity bought from the public grid. Moreover, PV plants could improve supply security through short-term island operation.
In future, inverters could take over grid management tasks and provide energy services. In addition to stabilizing voltage and frequency, these include controlling the power factor and the targeted production of harmonic components to improve grid quality.
For this reason, bidirectional network interfaces are required to ensure the necessary communications and to link the large number of decentralized suppliers and consumers together in “smart grids”. This is an important precondition for the power supply of the future, which will no longer be dominated by large fossil fuel or nuclear power plants but by a few centralized and many decentralized power generation units.
PV plants will then feed power into the public grid or the microgrid (individual households, for example) on demand. If supply considerably exceeds demand, the solar power will be stored locally. This turns the microgrids that communicate with each other into smart grids, which in turn play an important part within a controllable, virtual large-scale power plant.
Applications
Photovoltaics was originally used for supplying autonomous systems, mainly in aerospace applications. A satellite was first equipped with solar cells as early as 1958. After photovoltaics proved successful in space applications, it was soon used to power small devices for daily use, such as pocket calculators and watches, later even parking meters, traffic signs and solar lights.
In the mid 1970s, the first commercial, 20 to 30 W modules became available, creating larger stand-alone systems. In 1983, a village in the Philippines was the first village to be entirely supplied with solar power. In Europe, isolated farmhouses or hiking cabins were equipped with PV installations which had an output of between 1 and 4 kW. In response to the Chernobyl nuclear reactor disaster in 1986, private individuals started testing stand-alone solar power systems for single family homes. These projects were successful, but too costly to become widespread. Above all, storing electricity in batteries was too expensive.
As shown by the Australian annual solar mobile race, solar mobility is still in its experimental stage rather than a commercial sector. On many lakes, tourist boats are powered by special solar modules installed onto the roof of the passenger cabin. Unmanned zeppelins and solar planes whose wings are completely covered with solar cells have already been tested; a scientist is planning a trip around the world in a solar plane in a few years’ time.
The scalability of photovoltaics (from mini solar cells with just a few milliwatts output to large 360 W modules) has contributed to a wide variety of stand-alone systems around the world today. These range from minute applications (pocket calculators) to the electricity supply of remote settlements, or solar mobility.
Stand-alone systems play but a minor role due to the fact that they produce relatively little electricity. Since powerful inverters were developed in around 1990, and since the systematic subsidization of feeding solar power into the grid started in 2000, grid-connected photovoltaics has developed into the predominant method of solar power generation.
Its typical applications range from a roof-top PV system on a family home (from 1 kW) to large, free-field power plants with ten thousand times that output. The largest plants have an output of almost 100 MW, and an end to this growth in scale is not in sight.
Today, wherever fed-in solar power is remunerated well enough to cover the costs, available roof space is slowly but surely being used. PV modules are being installed on single and multi-family homes, on schools, agricultural buildings, factories, and warehouses. With falling investment costs, it is no longer just south-facing roofs that are suitable, but also east- and west-facing ones.
This increases the amount of solar power fed into the grid in the mornings and afternoons. The typical “noon peak” is thus evened out, and the feed-in period is lengthened. This makes the grid integration of solar power, whose production is naturally fluctuating, easier.





























