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1.2 Types of PV Cells

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Solar cells are the devices that convert sunlight into electricity. Solar cells are made of semiconductor materials and use a junction to separate the carriers of different charges, that is, to separate the electrons from the holes to create a voltage. There are a number of good articles on how solar cells work including one by the author [12] as well as others in print [13] and on line [14]. This book will not go into great detail about how solar cells work, but will discuss them in terms of how they impact the reliability of PV modules.

A variety of materials have been used commercially to make solar cells. The list below discusses those that have been successfully utilized in terrestrial PV modules and are available commercially today.

Crystalline silicon materials: Crystalline silicon materials were the first utilized for fabrication of solar cells by Bell Laboratories [7]. They were also the first used for space applications and then the first commercialized for remote power terrestrial applications. Crystalline silicon technology has been, and still is, the dominant commercial PV material, with more than 90% of the terrestrial PV market in 2018 [4].

Crystalline Si is a wafer‐based technology. Today, all of the commercial wafers are cut from ingots. There are two different types of crystalline silicon materials, single or mono‐crystalline and multi‐crystalline. They differ in the way the silicon ingots are grown. The single‐crystal ingots are grown by a crystal growth process called Czochralski (CZ), where a single‐crystal seed is dipped into a bath of molten silicon. As the seed is withdrawn, the silicon grows the same orientation as the seed. This is the same process that is used to make the wafers for many semiconductor devices. Single‐crystal ingots are round, but round wafers do not pack very well into rectangular modules so, in most cases, the round wafers are cut into square or pseudo‐square wafers for PV. Multi‐crystalline Si is grown using direction solidification in a crucible or mold. This process was developed specifically for PV in the late 1970s [15]. According to Paula Mints [4], in 2018 multi‐crystalline Si technology accounted for slightly more than 50% of the worldwide shipments of PV modules, while mono‐crystalline Si accounted for approximately 45%.


Figure 1.1 Cross‐sectional drawing of screen‐printed cry‐Si solar cell.

For both mono‐ and multi‐crystalline Si, the ingots are cut into wafers using wire saws. The resultant wafers are then processed into cells and the cells incorporated into modules in very similar ways. There are a number of cell processes in use today. Let's take a look at screen‐print technology (one of the simpler methods) since most of the cell components will be similar no matter which cell design is used. Figure 1.1 shows a diagram of the important features of a screen‐printed cry‐Si solar cell.

The solar cell is fabricated on the Si wafer. A p‐n junction is grown in the front (sun side) usually by diffusion. Metal grid lines are printed on the front to collect the current generated by the cell. The back side is also metallized. The drawing shows continuous back metallization though a grid can also be used on the back. Finally, because bare silicon is quite reflective, an antireflective coating (AR) is usually applied to the front. For mono‐crystalline Si the front surface is usually textured to increase optical absorption. This is one of the reasons that mono‐crystalline cells are usually a few percent higher in efficiency than multi‐crystalline cells. It is important to remember the different components in the cell when addressing reliability, because it is usually not the Si wafer or the p‐n junction that degrade, but rather the contacts, the interconnections between cells or even the AR coating.

Screen‐printed cry‐Si cells are typically fabricated on 15.6 × 15.6 cm wafers. Over the years, the wafer thickness has been slowly reduced to lower the cost of the Si used in the module. Today, Si wafers are typically less than 200 μm thick, which makes them more susceptible to breakage than the thicker wafers that were used in the earlier days of PV. Today most commercial screen‐printed cells have a conversion efficiency in the range of 15–19% with the multi‐crystalline Si cells at the low end and monocrystalline Si cells at the high end.

A number of commercial cell manufacturers have utilized specialty structures in order to increase cell performance. Several examples are:

 SunPower has commercialized cells with all of the contacts on the back of the cell. This cell structure eliminates front surface shadowing and can provide improved collection of the high currents associated with large area cells. This cell structure requires silicon substrates with very high lifetimes and excellent front surface passivation. SunPower offers their commercial cells with conversion efficiency up to 22.7% [16].

 The HIT (Heterojunction with intrinsic thin layer) cell uses heterojunctions between a‐Si and crystalline silicon to produce a much higher voltage than the standard p‐n junction. So HIT cells have high efficiency with research cells reported at 25.6% [17] and commercial modules available from Panasonic with reported efficiencies of 19.7% [18].

 One of the latest methods for increasing cell efficiency is the use of PERC Technology (Passivated emitter rear cell). PERC cells use the same screen‐printed front surface as standard screen‐print technology, but the rear is modified by replacing the full metal coverage with a passivated dielectric layer with small area back contacts. PERC improves the cells by reducing the back‐surface recombination of carriers and improving the reflection of long wavelength light back into the cells [19]. Solar World has reported PERC cell efficiencies of 22% [20]. There have been a number of forecasts that PERC will gain significant market share in the next few years.

Each solar cell produces a voltage determined by the semiconductor junction. For crystalline Si the typical p‐n junction cell has an open circuit voltage of 0.6–0.7 V and a peak power voltage of around 0.5 V. Therefore, to reach useful voltages a number of cells are connected together in series into a module. Each cell has metal contacts typically copper ribbons attached to the front metal grid and then to the back metallization of the next cell in the string. Ribbons from the front of the cell before it in the string are attached to its back metallization. In this way cell voltages are combined to reach useful levels. Today, most cry‐Si power modules have 60 or 72 cells in series. The next section will talk about the module packaging in more detail.

Thin Films Materials: In the thin‐film approach, the various layers of a PV device are deposited directly onto a substrate or superstrate. The advantages of thin films are the potential ability to:

 Dramatically reduce the amount of material utilized. In some cases, the active semiconductor only needs to be a fraction of a micron thick in order to absorb most of the incident sunlight.

 Directly integrate into a higher voltage module, thereby eliminating much of the handling and labor necessary to produce cry‐Si modules.

For monolithically integrated thin film modules, the deposition processes and the integration processes are described in Table 1.1 and the resultant structure shown in cross section in Figure 1.2. Figure 1.2 is not drawn to scale as the thin film layers and the three different scribe lines are exaggerated in size so you can see them. In thin film devices, the semiconductors have considerably higher resistance than cry‐Si so metal grids do not work well. Instead, a Transparent Conductive Oxide (TCO) is often used on the semiconductor surface to provide a conductive path as well as serving as the AR. Because the TCO layers are not as conductive as a metal grid, thin film solar cells are usually long and skinny, so that the collected current only flows a short distance across the cell to the next cell. Monolithically integrated thin film modules often have a large number of skinny cells connected in series, resulting in higher voltage, lower current and reduced series resistance losses.

Thin film layers of materials are more susceptible to corrosion than bulk materials. When thin film layers are deposited directly in contact with glass, they may also be susceptible to ion flow in the glass [21]. This is why many thin film modules are protected in packages that are designed to keep moisture out for the lifetime of the product.

Table 1.1 Process for making monolithically integrated thin film modules.

Step # Step Name Description
1 Transparent Conductive Oxide TCO Deposit TCO layer onto the substrate
2 P1 Scribe Scribe to remove TCO from selected areas
3 Semiconductor Deposition Deposit the semiconductor layers that make the solar cells
4 P2 Scribe Scribe to remove the Semiconductors from selected areas
5 Metallization Deposit the back metallization
6 P3 Scribe Scribe to remove the Metallization from selected areas

Figure 1.2 Cross‐sectional drawing of monolithically integrated thin film module.

According to Mints [4], thin films only represented about 5% of total worldwide module shipments in 2018, a declining percentage from previous years. The thin‐film PV commercial market includes the following three materials.

1 Cadmium telluride (CdTe): CdTe is a well‐known semiconductor often used in high performance infrared (IR) sensors. CdTe absorbs visible light very strongly, so very thin films (1–2 μm) are sufficient to absorb most of the sunlight. Commercial CdTe modules are typically fabricated on glass with a structure similar to the cross‐sectional drawing in Figure 1.2. First Solar is by far the largest supplier of CdTe modules. First Solar now offers large area, monolithically integrated CdTe modules with efficiencies of up to 18% [22]. CdTe technology is especially attractive because of low‐cost manufacturing. In 2018, First Solar, selling just CdTe modules shipped about 3% of the world's PV modules [4].

2 Copper Indium Diselenide (CIS) and Copper Indium Gallium Diselenide (CIGS): Both CuInSe2 (CIS) and Cu(InGa)Se2 (CIGS) are ideal PV‐absorber materials. The band gap is near the optimum for absorbing the terrestrial spectrum. These materials have strong optical absorption so very thin films (~1 μm) are sufficient to absorb most of the sunlight. Grain boundaries and surfaces in CIS and CIGS are electronically benign, so simple polycrystalline films yield reasonably high efficiency PV devices without complex grain boundary passivation. Typical CIS and CIGS cells use thin CdS layers to form p‐n junctions, molybdenum for ohmic contacts to the CIS or CIGS, and transparent conductors like zinc oxide and indium‐tin oxide for contact to the CdS and to serve as an AR coating. In most cases, CIS and CIGS cells are deposited upside down, meaning that the back metal is deposited first and the cells are deposited from back to front onto the metal. So, CIS and CIGS modules often have the cells deposited onto the back glass of a glass/glass package or onto a metallic substrate that is then diced up to produce individual cells that are packaged like you would wafer‐based cells. While CIS and CIGS are attractive PV materials, it has taken a long time to move from the laboratory to commercialization. Two reasons for this appear to be the difficultly in scaling to larger sizes and larger volumes, related to uniformity of the deposited films, and sensitivity to environmental stresses. Reliability issues relate to the humidity sensitivity of the contacts and TCO necessitating hermetic sealing to achieve long‐term life. Solar Frontier from Japan is the world's largest manufacturer of CIS PV modules offering large area, monolithically integrated CIS modules with conversion efficiencies up to 15% [23]. In 2018, CIS/CIGS made up about 1% of the worldwide shipments of PV modules [4].

3 Amorphous Silicon (a‐Si): Alloys of a‐Si made of thin‐film hydrogenated silicon (a‐Si:H) can be deposited on either glass superstrates or flexible metallic substrates. Because of the low minority carrier lifetimes in doped a‐Si, p‐i‐n (p‐type, intrinsic, n‐type) cell structures are utilized rather than normal p‐n junctions. Even in undoped a‐Si, the minority carrier lifetimes are short and because of the Staebler‐Wronski effect, in which light induces additional electrically active defects, the thickness of individual layers must be minimized. Therefore, to achieve reasonable efficiencies, multi‐junctions are usually utilized. Commercial a‐Si is typically fabricated with a structure similar to the cross‐sectional drawing in Figure 1.2. The maximum reported efficiency for a‐Si modules is about 12% [17], which is less than the efficiencies of commercially available CdTe or CIGs modules. Commercial a‐Si modules have efficiencies in the 5–8% range after light stabilization. Most a‐Si products are used in consumer‐type products (watches, calculators, etc.) not for power production.

Over the years, there have been a number of efforts to use optical concentration to increase the output power that can be obtained from PV devices. Some of these efforts have resulted in laboratory systems with high efficiencies and good performance. However, to date, none have been able to establish a sustainable commercial market. For this reason, reliability of concentrator PV will not be discussed in this book.

Photovoltaic Module Reliability

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