WO2011097676A1 - Composition de contact - Google Patents
Composition de contact Download PDFInfo
- Publication number
- WO2011097676A1 WO2011097676A1 PCT/AU2011/000137 AU2011000137W WO2011097676A1 WO 2011097676 A1 WO2011097676 A1 WO 2011097676A1 AU 2011000137 W AU2011000137 W AU 2011000137W WO 2011097676 A1 WO2011097676 A1 WO 2011097676A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nickel
- aluminium
- silicon
- μπι
- dopant polarity
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 339
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 169
- 239000004065 semiconductor Substances 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims abstract description 41
- 229910052751 metal Inorganic materials 0.000 claims abstract description 30
- 239000002184 metal Substances 0.000 claims abstract description 30
- 229910000838 Al alloy Inorganic materials 0.000 claims abstract description 23
- 239000000463 material Substances 0.000 claims abstract description 12
- 239000010409 thin film Substances 0.000 claims abstract description 9
- 239000004411 aluminium Substances 0.000 claims description 142
- 229910052782 aluminium Inorganic materials 0.000 claims description 142
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 142
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 100
- 229910052710 silicon Inorganic materials 0.000 claims description 100
- 239000010703 silicon Substances 0.000 claims description 100
- 239000002019 doping agent Substances 0.000 claims description 62
- 229920005989 resin Polymers 0.000 claims description 36
- 239000011347 resin Substances 0.000 claims description 36
- 239000010408 film Substances 0.000 claims description 33
- 238000002955 isolation Methods 0.000 claims description 26
- 229910045601 alloy Inorganic materials 0.000 claims description 20
- 239000000956 alloy Substances 0.000 claims description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 238000005538 encapsulation Methods 0.000 claims description 16
- 229920003986 novolac Polymers 0.000 claims description 12
- 239000011521 glass Substances 0.000 claims description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical group [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 10
- 239000003518 caustics Substances 0.000 claims description 10
- 238000005530 etching Methods 0.000 claims description 10
- 238000004544 sputter deposition Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 238000005477 sputtering target Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 230000007797 corrosion Effects 0.000 abstract description 3
- 238000005260 corrosion Methods 0.000 abstract description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 20
- 238000009413 insulation Methods 0.000 description 16
- 150000004767 nitrides Chemical class 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- QPJSUIGXIBEQAC-UHFFFAOYSA-N n-(2,4-dichloro-5-propan-2-yloxyphenyl)acetamide Chemical compound CC(C)OC1=CC(NC(C)=O)=C(Cl)C=C1Cl QPJSUIGXIBEQAC-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
- 239000012286 potassium permanganate Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical group COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 3
- 238000007641 inkjet printing Methods 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 238000000608 laser ablation Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000001579 optical reflectometry Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005389 semiconductor device fabrication Methods 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/0445—PV modules or arrays of single PV cells including thin film solar cells, e.g. single thin film a-Si, CIS or CdTe solar cells
- H01L31/046—PV modules composed of a plurality of thin film solar cells deposited on the same substrate
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/0445—PV modules or arrays of single PV cells including thin film solar cells, e.g. single thin film a-Si, CIS or CdTe solar cells
- H01L31/046—PV modules composed of a plurality of thin film solar cells deposited on the same substrate
- H01L31/0463—PV modules composed of a plurality of thin film solar cells deposited on the same substrate characterised by special patterning methods to connect the PV cells in a module, e.g. laser cutting of the conductive or active layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/0445—PV modules or arrays of single PV cells including thin film solar cells, e.g. single thin film a-Si, CIS or CdTe solar cells
- H01L31/046—PV modules composed of a plurality of thin film solar cells deposited on the same substrate
- H01L31/0465—PV modules composed of a plurality of thin film solar cells deposited on the same substrate comprising particular structures for the electrical interconnection of adjacent PV cells in the module
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/075—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PIN type, e.g. amorphous silicon PIN solar cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/548—Amorphous silicon PV cells
Definitions
- the present invention relates generally to the field of semiconductor device fabrication and in particular the invention provides an improved processing step for use in a method of forming metal contacts to semiconductor devices and in particular to thin film semiconductor devices such as thin film photovoltaic devices.
- PV photovoltaic
- the present invention provides a method of forming a connection layer, in an electronic device, the method comprising the steps of:
- connection layer a) preparing a surface onto which the connection layer will be formed
- the present invention provides a semiconductor device comprising a region of semiconductor material and a metal contact in electrical contact with the semiconductor layer, the metal contact comprising a connection layer of nickel:aluminium alloy.
- the device is a thin film silicon solar cell.
- the method of applying the connection layer is by sputtering.
- the electronic, device will be a photovoltaic device structure in a silicon film deposited on a glass substrate.
- the silicon film may comprise a first doped region having silicon of a first dopant polarity closest to the glass, a lightly doped or intrinsic region over the first doped region and a second doped region having silicon of a second dopant polarity opposite to the first dopant polarity over the lightly doped region.
- the method preferably further comprises One or more of the following steps: 1) dividing the silicon film into a plurality of cell regions by forming cell isolation grooves;
- the photovoltaic device structure may further comprise one or more of the following features:
- the nickehaluminium alloy layer extending over a surface of the organic resin layer and extending into each opening of the first set of openings to contact the silicon of the first dopant polarity and extending into the second set of openings to contact the silicon of the second dopant polarity, the alloy in the first set of openings being isolated from the exposed edges of the silicon of the second dopant polarity by the re-flowed resin;
- isolation grooves in the alloy layer to separate the contacts to the silicon of the first dopant polarity from the contacts to the silicon of the second dopant polarity within each cell, whereby the alloy layer interconnects the silicon of the second dopant polarity of one of the cells to the silicon of the first dopant polarity of an adjacent one of the cells;
- the nickel :aluminium alloy contact may be formed by various methods but one particularly preferred method is by sputtering.
- the nickel:aluminium alloy will have a composition of in the range of one of 10 - 100,000 or 100 - 100,000 or 1,000 - 100,000 or 10,000 - 100,000 or 10 - 10,000 or 100 - 10,000 parts per million nickel in aluminium (by weight) and preferably 1,000 - 10,000 or 2,000 - 10,000 or 3,000 - 10,000 or 4,000 - 10,000 or 5,000 - 10,000 or 6,000 - 10,000 or 7,000 - 10,000 or
- the sputtering source When applying the contact by sputtering the sputtering source will be a nickel:aluminium target having a composition comprising the desired composition of the contact.
- the nickehaluminium alloy may be in the range of one of 90.000 - 99.999% aluminium and 0.001 - 10.000% nickel or 99.000 - 99.999% aluminium and 0.001 - 1.000% nickel or 99.900 - 99.999% aluminium and 0.001 - 0.100% nickel or 99.990 - 99.999% aluminium and 0.001 - 0.010% nickel or 90.000 - 99.990% aluminium and 0.010 - 10.000% nickel or 99.000 - 99.990% aluminium and 0.010 - 1.000% nickel or 99.900 - 99.990% aluminium and 0.010 - 0.100% nickel 90.000 - 99.900% aluminium and 0.100 - 10.000% nickel or 99.00 - 99.900% aluminium and 0.100 - 1.000% nickel or 90.000
- the composition of the nickel :aluminium alloy target is selected to obtain low resistance contacts to both dopant polarities of the cell while maintaining good corrosion protection properties.
- the sputtered layer of nickel :aluminium alloy may be in the range of one of
- the method of the third aspect further includes the step of etching the silicon film in the second set of openings to remove damaged material from the surface of the silicon of the second dopant polarity before formation of the metal layer.
- the organic resin is preferably novolac, but other similar resins are also suitable such as commonly available photoresists.
- the openings in the resin layer can be formed by chemical removal using solutions of caustic substances such as potassium hydroxide (KOH) or sodium hydroxide (NaOH). Other methods of making openings in the mask layer include laser ablation and photographic techniques (using photoresist).
- Fig. 1 is a diagram of a section through a semiconductor device after initial steps of applying an anti-reflection coating over a glass substrate and depositing a doped semiconductor film over the anti-reflection coating;
- Fig. 2 is the sectional view seen in Fig. 1 after a scribing step has been completed to form a cell separating groove dividing separate cell areas and insulating layers have been applied over the semiconductor layer;
- Fig. 3 is a schematic diagram of an X-Y table with an inkjet print head fitted for directly applying the insulation etchant , using inkjet technology;
- Fig. 4 is the sectional view seen in Fig. 2 (shifted slightly to the left), after a pattern of etchant has been directly deposited onto the insulating layer to open the insulating layer in areas where contacts to an underlying n + type region of the semiconductor layer are required;
- Fig. 5 is the sectional view seen in Fig. 4 after the insulation layer has been opened in the areas where contacts to the underlying n + type region of the semiconductor layer are required;
- Fig. 6 is the sectional view seen in Fig. 5 after further etching steps have been performed to remove some of the doped semiconductor film in the area where the contact to the underlying n + type region of the semiconductor layer is required;
- Fig. 7 is the sectional view seen in Fig. 6 after a reflow step to flow some of the insulating layer into the hole formed by removal of some of the doped semiconductor film in the area where a contact to the underlying n + type region of the semiconductor layer are required.
- a pattern of caustic solution has been directly deposited onto the insulating layer to open the insulating layer in an area where a contact to an upper p + type region of the semiconductor layer is required;
- Fig. 8 is the sectional view seen in Fig. 7 after the caustic has opened the insulation layer in the areas where the contact to the upper p + type region of the semiconductor layer is required;
- Fig. 9 is the sectional view seen in Fig. 8 after further etching steps have been performed to clean the surface of the doped semiconductor film of damaged material in the areas where the contact to the upper p + type region of the semiconductor layer is required;
- Fig. 10 is the sectional view seen in Fig. 9 after a metal layer has been applied to contact the p + and n + type regions of the semiconductor material and to interconnect adjacent cells;
- Fig. 11 is the sectional view seen in Fig. 10 after the metal layer has been interrupted to separate the contacts to the p + & n + type regions from each other within each cell;
- Fig. 12 is a back view (silicon side) of part of the device of Fig. 11 ; and Fig. 13 is a diagram of a part of a completed device, illustrating the interconnection between adjacent cells and the encapsulation layer.
- Fig. 1 illustrates a part of a semiconductor structure
- the semiconductor structure 11 which is a precursor to the photovoltaic device fabrication process described below.
- the semiconductor structure 11 is formed as a thin semiconductor film applied to a substrate 22 in the form of a glass sheet to which a thin silicon nitride anti-reflection coating 71 has been applied.
- the thin semiconductor film comprises a thin polycrystalline silicon film 12 formed with a total thickness in the range of 1 to 2 ⁇ and preferably ⁇ . ⁇ .
- the polycrystalline silicon film 12 has an upper p + type region 13 which is 60nm thick, a lower n + type region 15 which is 40nm thick, and a 1.5 ⁇ thick intrinsic or lightly p type doped region 14 separating the p + and n + type regions.
- the sheet resistance in both n + type and p + type layers is preferably between 400 and 2500 ⁇ / ⁇ , with no more than 2xl0 14 cm "2 boron in total. Typical values are around 750 ⁇ D for n + type material and 1500 ⁇ /D for p + type material.
- the thickness of the n + type and p + type layers is typically between 20 and 100 ran.
- the glass surface is preferably textured to promote light trapping, but this is not shown in the drawings for sake of clarity.
- the silicon film 12 is separated into cells by scribed isolation grooves 16. This is achieved by scanning a laser over the substrate in areas where isolation grooves 16 are required to define the boundaries of each photovoltaic cell. To scribe the grooves 16, the structure 11 is transferred to an X-Y stage (not shown) located under a laser operating at 1064 nm to produce focussed laser beam 73 which cuts the isolation grooves through the silicon. The laser beam is focussed to minimise the width of the groove, which is lost active area. Typically, a pulse energy of 0.11 mJ is required to fully ablate the silicon film and gives a groove width of 50 ⁇ . To ensure a continuous groove, successive pulses are overlapped by 50%. The optimum cell width is in the range of 5 to 8 mm and cell widths of 6mm are typical.
- the first insulation layer is an optional thin but tough cap nitride 72. This layer protects the exposed silicon along the edges of the cell definition grooves 16 after laser scribing and passivates the surface of the silicon.
- the cap nitride 72 is preferably capable of being etched completely in a few minutes to allow access to the silicon at n type and p type contact locations and typically comprises 60 nm of silicon nitride deposited by PECVD at a temperature of 300 - 320°C.
- the structure 11 is transferred to a tank containing a 5% solution (by weight) of hydrofluoric acid for one minute. This removes any remaining debris and any surface oxides that may have formed. The structure is rinsed in de-ionised water and dried.
- the second insulation layer 17 is a thin layer of organic resin.
- the insulating resin is resistant to dilute solutions of hydrofluoric acid (HF) and potassium permanganate ( ⁇ 4), and is preferably vacuum compatible to 10 "6 mbar.
- the insulation material most often used is novolac resin (AZ PI SO) similar to that used in photoresist (but without any photoactive compounds).
- the novolac resin is preferably loaded with 20 - 30% (by weight) white titania pigment (titanium dioxide) which improves coverage and gives it a white colour that improves its optical reflectivity to help trap light within the silicon.
- the resin layer 17 serves as an etch mask for etching steps described below and also covers over the rough jagged surface that is formed along the edges of the cell definition grooves 16, an area that is prone to pinholes in the cap nitride layer 72.
- the organic resin layer 17 also thermally and optically isolates the metal layer from the silicon to facilitate laser patterning of a metal layer in contact forming process steps described below.
- the novolac resin is applied to each module to a thickness of 4 to 5 ⁇ using a spray coater. After the structure 11 is coated, it is passed under heat lamps to heat it to 90°C to cure. As seen in Fig. 2, the insulation layer 17 is applied over the cap layer 72 and extends into the cell separation grooves 16.
- ink-jet technology is used to open holes in the novolac resin layer 17 at the crater locations.
- the structure 11 is loaded onto an X-Y stage equipped with an ink-jet head 91 having multiple nozzles with a nozzle spacing of 0.5 mm and controlled by controller 92.
- the glass is held down with a vacuum chuck and initially scanned to ensure that no point is deformed more than 1 mm above the stage.
- the glass is then scanned beneath the head 91 at a table speed of typically 400 mm/s.
- Droplets 76 of dilute (15% +/- 1% by weight) potassium hydroxide (KOH) (see figure 4) are dispensed at locations intended for n type 'crater' contacts.
- the odd-numbered nozzles fire in the odd-numbered cells, and the even-numbered nozzles fire in the even-numbered cells, so that within a given cell, the spacing between lines of droplets is 1 mm.
- the spacing between droplets within each line is 400 ⁇ , hence the rate of droplet release at a table speed of 400 mm/s is 1 kHz.
- the droplets are sized to etch circular openings in the resin layer that are about 100 ⁇ in diameter.
- the KOH solution removes the resin insulation 17 in the area of the droplet 76 after a few minutes to form the hole 32 seen in Fig. 5.
- the openings 32 are spaced holes so that lateral continuity is maintained in the semiconductor layer after contact formation.
- the ink-jet printing process applies a droplet 76 of the caustic solution in a controlled manner to remove the insulation only where the n type contacts are to be formed.
- the caustic solution preferably contains potassium hydroxide (KOH) but can also use sodium hydroxide (NaOH) and includes glycerol for viscosity control.
- KOH potassium hydroxide
- NaOH sodium hydroxide
- the print head used for this purpose is a model 128ID, 64ID2 or 64-30 manufactured by Ink Jet Technologies Inc., and will print substances having a viscosity in the range 5 to 20 centipoise.
- the droplet size deposited by the print head is in the range of 20 to 240 picolitre corresponding to a deposited droplet diameter range of 50- 150uin.
- the droplets are printed at a diameter of ⁇ .
- novolac is an organic resin closely related to the resins used in photo-resist material and the etchant printing process described above will apply equally to the patterning of other such materials.
- the structure 11 is rinsed in water to remove residual KOH from the ink-jet printing process, and it is then immersed in a tank containing a 5% solution (by weight) of hydrofluoric acid for 1 minute to remove the silicon nitride from the n type contact openings 32.
- the sheet is then directly transferred to a tank containing 1% hydrofluoric acid (HF) and 0.1% potassium permanganate (KMnO.)) (by weight) for 4 minutes.
- HF hydrofluoric acid
- KMnO. potassium permanganate
- the structure 11 is then rinsed in de-ionised water and dried.
- the resulting opening 32 in the silicon 12 has a rough bottom surface 82, in which some points may be etched through to the anti-reflection layer 71 and some ridges 83 extend into the lightly doped p type region 14 as seen in Fig. 6.
- Jong as some of the n + type region is exposed, good contact can be made to the n + type region. Because the p type region is very lightly doped in the area near the n + type region there is insufficient lateral conductivity to cause shorting if some p type material is also left in the bottom of the hole 32.
- the walls need to be insulated to prevent shorting of the p-n junction. This is achieved by causing the insulation layer 17 to re-flow whereby a portion of the insulation layer 78 in the vicinity of the edge of the opening 32 flows into the hole to form a covering 79 over the walls as seen in Fig.7.
- the sheet is passed through a zone containing a vapour of a suitable solvent. This causes the novolac resin of the insulating layer 17 to reflow, shrinking the size of the . crater openings 32. As the samples exit this zone, they are heated under heat lamps to a temperature of 90°C to drive out die remaining solvent.
- the rate of re-flow will vary with the aggressiveness of the solvent used, the concentration and, temperature.
- suitable, volatile solvents that will dissolve organic resins such as novolac, including substances such as acetone.
- Acetone is a suitable solvent for the process, but acts quite aggressively, requiring only a few seconds to cover the walls of the hole 32 with resin, and making it difficult to control the process accurately.
- the preferred solvent is propylene glycol monomethyl ether acetate (PGMEA) and the device is introduced into an atmosphere containing a saturated vapour of PGMEA at room temperature (e.g., 21° C) for 4 minutes until a slight shrinkage of the holes in the insulation is observed.
- PGMEA propylene glycol monomethyl ether acetate
- a further set of holes 19 are then formed in the insulation layer 17, again using the printing and etching process described above with reference to figs. 3, 4 and 5. These openings are formed by printing droplets 81 of caustic solution onto the insulation (see Fig. 7) in the locations where p type contact "dimples" are required. Following the removal of the insulation layer 17 by the caustic solution to form the openings 19 (see Fig. 8), any residual caustic solution is washed off with water and the cap layer 72 removed in the openings 19 with an etch of 5% hydrofluoric acid (HF) (by weight) for 1 minute (note times of from 10 seconds to 10 minutes may be required to remove the nitride layer depending on its stoichiometry).
- HF hydrofluoric acid
- any damaged silicon material on the surface of the p + type region 13 is then removed to allow good contact using an etch in 1% hydrofluoric acid (HF) and 0.1% potassium permanganate (KMnO-i) (by weight) for ten seconds followed by a rinse in de-ionised water to provide the slightly recessed contact "ciimple" 85 seen in Fig. 9.
- This length of etch is long enough to remove surface plasma damage without etching all the way through the p + type layer 13. It is also short enough to have negligible impact on the n type contacts.
- the final stage of device fabrication involves depositing a metal layer and slicing it up So that it forms a plurality of independent electrical connections, each one collecting current from one line of p type dimple contacts and delivering it to a line of n type crater contacts in the adjacent cell. In this manner, monolithic series interconnection of the cells is achieved.
- the structure 11 Before the metal layer is applied, the structure 11 is immersed into a tank containing a 0.2% solution (by weight) of hydrofluoric acid for 20 seconds. This acid removes the surface oxide from both the crater and dimple contacts. There is wide latitude for the strength and duration of this etch and hydrofluoric acid solution strengths of in the range of 0.05 to 0.5% (by weight) can be used by compensating the time of the etch within the range of 5 to 100 seconds. The structure is then rinsed in de-ionised water and dried.
- the contact metal for the n type and p type contacts is applied simultaneously by depositing a thin metal layer 28 over the insulation layer 17 and extending into the holes 32 and 19 to contact the surfaces 82 and 85 of the n + type region 15 and p + type region 13.
- the metal layer is preferably a thin layer of nickel:aluminium alloy, which makes good electrical contact to both n + type and p + type silicon, provides good lateral conductivity, and has high optical reflectance.
- the nickel.aluminium alloy contact may be formed by various methods but one particularly preferred method is by sputtering.
- the nickel:aluminium alloy will have a composition of in the range of 10 - 100,000 parts per million nickel in aluminium and preferably 1000 - 10000 parts per million nickel in aluminium (by weight).
- the sputtering source When applying the contact by sputtering, the sputtering source will be a nicke aluminium target having a composition comprising the desired composition of the contact.
- the the nickel.aluminium alloy may be in the range of one of 90.000 - 99.999% aluminium and 0.001 - 10.000% nickel and preferably will be in the range of 99.0 - 99.9% aluminium and 0.1 - 1% nickel (by weight)
- the sputtered layer of nicke aluminium alloy may be in the range 0.05-0.5 um and preferably nominally 0.1 um (0.095 - 0.105 um) thick.
- the isolation of the n type and p type contacts is achieved by using a laser 86 (see Fig. 10) to melt and/or evaporate the metal layer 28 to thereby form an isolation groove 31 as seen in Fig. 11.
- a laser 86 see Fig. 10
- a small amount of metal is ablated directly under the beam creating a hole 31.
- the structure 11 is processed using a laser operating at 1064 nm to scribe the isolation grooves in the metal layer 28.
- the laser is adjusted so that it scribes through the metal layer 28 without damaging the silicon 12.
- These scribes 31 separate the n type contacts 32 from the p type contacts 19 within each cell, while retaining the series connection of each cell to its neighbours.
- Preferred laser conditions are a pulse energy of 0.12 mJ with the beam defocused to a diameter of about 100 ⁇ .
- the pulse overlap is 50% and the scribes are spaced 0.5 mm apart.
- Fig. 12 illustrates a rear view of a part of a device made by the process described above, from which it can be seen that each of the cells of the device 11 comprises an elongate photovoltaic element 35a, 35b, 35c, 35d divided across its long axis by a plurality of transverse metal isolation scribes 31 which isolate alternate sets of holes 19 and holes 32 respectively providing contacts to the p + type and n + type regions of the cell.
- the transverse scribes 31 are made as long substantially straight scribes extending over the length of the device such that each scribe crosses each elongate cell.
- a further set of metal isolation scribes 34 are formed over the cell separation scribes 16 between adjacent cells 11, to isolate every second pair of cells.
- the metal isolation scribes 34 extending to either side of any one of the elongate transverse scribes 31 are offset by one cell with respect to those on the other side of the same transverse scribe 31 such that the cells become series connected by a matrix of connection links 36 with alternating offsets, connecting one set of p type contacts 19 of one cell 35 to a set of n type contacts 32 of an adjacent cell 35, as shown in Figure 12.
- the metal isolation scribes 31 comprises a first set of long scribes transverse to the cells 35 from 50-200 ⁇ wide, preferably about ⁇ wide.
- the scribes are typically spaced on centres of 0.2-2.0mm and preferably about 0.5mm to form conducting strips about 0.2-1.9mm and preferably about 0.4mm wide.
- the isolation scribes 34 comprises a second set of interrupted scribes parallel to the long direction of the cells 35 and substantially coincident with the cell isolation grooves 16 in the silicon,
- the isolation scribes 34 are also from 50-200 ⁇ wide, preferably about ⁇ wide. It is equally possible to form the isolation scribes 34 before forming the transverse isolation scribes 31.
- the scribed areas are illustrated in Fig. 12 with cross-hatching.
- FIG. 13 which illustrates a portion of the completed structure, the device is typically encapsulated in an encapsulation film 88 such as a 0.4 mm thick EVA encapsulation or a 0.2 mm thick Tedlar-Polyester-EVA (TPE) encapsulation.
- Fig. 13 also shows the connection of an n type contact of one cell to the p type contact of an adjacent cell to provide a series connections of cells. In practice there may be several n type contacts grouped together and several p type contacts grouped together however for the sake of clarity only one of each is shown in each cell.
- the arrangement shown in Fig. 13 is also schematic as the isolation grooves 16 in the silicon and the isolation grooves 31 in the metal run perpendicularly to one another in practice as is seen in Fig. 12.
Landscapes
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Sustainable Development (AREA)
- Computer Hardware Design (AREA)
- Power Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
- Physics & Mathematics (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Sustainable Energy (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
L'invention concerne un procédé de fabrication de contacts et de formation d'une couche de conduction dans un dispositif semi-conducteur, en particulier dans des dispositifs semi-conducteurs à couche mince comme des dispositifs photovoltaïques à couche mince. Le processus produit une zone de matériau semi-conducteur en contact avec une couche de contact métallique, la couche de contact métallique comprenant une couche d'alliage de nickel et d'aluminium. L'alliage de nickel et d'aluminium établit le contact avec le dispositif et l'interconnecteur de dispositifs individuels avec une résistance supérieure à la corrosion.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2010900612 | 2010-02-15 | ||
AU2010900612A AU2010900612A0 (en) | 2010-02-15 | Contact composition |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011097676A1 true WO2011097676A1 (fr) | 2011-08-18 |
Family
ID=44367057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/AU2011/000137 WO2011097676A1 (fr) | 2010-02-15 | 2011-02-10 | Composition de contact |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2011097676A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102938427A (zh) * | 2012-11-27 | 2013-02-20 | 宁波贝达新能源科技有限公司 | 一种光伏电池组件 |
CN102965549A (zh) * | 2012-11-27 | 2013-03-13 | 宁波贝达新能源科技有限公司 | 光伏电池组件用背板材料 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05160420A (ja) * | 1991-12-04 | 1993-06-25 | Sharp Corp | 太陽電池 |
US5595607A (en) * | 1991-12-09 | 1997-01-21 | Unisearch Limited | Buried contact interconnected thin film and bulk photovoltaic cells |
EP0694213B1 (fr) * | 1994-02-17 | 2004-04-21 | RWE Schott Solar Inc. | Procede de fabrication de modules de cellules solaires |
WO2009038323A2 (fr) * | 2007-09-17 | 2009-03-26 | Jusung Engineering Co., Ltd. | Pile solaire et son procédé de fabrication |
US20090317938A1 (en) * | 2003-09-09 | 2009-12-24 | Csg Solar Ag | Adjustment of masks by re-flow |
-
2011
- 2011-02-10 WO PCT/AU2011/000137 patent/WO2011097676A1/fr active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05160420A (ja) * | 1991-12-04 | 1993-06-25 | Sharp Corp | 太陽電池 |
US5595607A (en) * | 1991-12-09 | 1997-01-21 | Unisearch Limited | Buried contact interconnected thin film and bulk photovoltaic cells |
EP0694213B1 (fr) * | 1994-02-17 | 2004-04-21 | RWE Schott Solar Inc. | Procede de fabrication de modules de cellules solaires |
US20090317938A1 (en) * | 2003-09-09 | 2009-12-24 | Csg Solar Ag | Adjustment of masks by re-flow |
WO2009038323A2 (fr) * | 2007-09-17 | 2009-03-26 | Jusung Engineering Co., Ltd. | Pile solaire et son procédé de fabrication |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102938427A (zh) * | 2012-11-27 | 2013-02-20 | 宁波贝达新能源科技有限公司 | 一种光伏电池组件 |
CN102965549A (zh) * | 2012-11-27 | 2013-03-13 | 宁波贝达新能源科技有限公司 | 光伏电池组件用背板材料 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7446051B2 (en) | Method of etching silicon | |
US7960206B2 (en) | Adjustment of masks by re-flow | |
US7585781B2 (en) | Method of forming openings in an organic resin material | |
US10290750B2 (en) | Systems and methods for forming foil contact rear emitter solar cell | |
US8846431B2 (en) | N-type silicon solar cell with contact/protection structures | |
EP2748858A1 (fr) | Processus et structures d'ablation par laser à haut débit pour former des trous de contact dans des cellules solaires | |
JP7471229B2 (ja) | レーザービームを使用した半導体基板の局所メタライゼーション | |
WO2011097676A1 (fr) | Composition de contact | |
TWI496308B (zh) | Thin film solar cell and manufacturing method thereof | |
US20110177651A1 (en) | Method for producing a metal structure on a surface of a semiconductor substrate | |
US6544865B1 (en) | Metal film interrupting process | |
AU2004271223B2 (en) | Improved method of etching silicon | |
AU2004271224B2 (en) | Adjustment of masks by re-flow | |
AU2004271225B2 (en) | Improved method of forming openings in an organic resin material | |
JP5275415B2 (ja) | 結晶太陽電池セルおよび結晶太陽電池セルの製造方法 | |
US11949037B2 (en) | Local patterning and metallization of semiconductor structures using a laser beam | |
JP5677404B2 (ja) | 結晶太陽電池セル | |
JP5129369B2 (ja) | 結晶太陽電池セルおよび結晶太陽電池セルの製造方法 | |
JP2009130109A (ja) | 太陽電池セルの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 11741751 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 11741751 Country of ref document: EP Kind code of ref document: A1 |