PHOTOVOLTAIC CELL STRUCTURE AND METHOD OF MANUFACTURING A PHOTOVOLTAIC CELL
20170069772 ยท 2017-03-09
Inventors
- Sylwia GIERALTOWSKA (Warszawa, PL)
- Marek GODLEWSKI (Warszawa, PL)
- Grzegorz LUKA (Rzeszow, PL)
- Rafal PIETRUSZKA (Wilczyce, PL)
- Lukasz WACHNICKI (Warszawa, PL)
- Bartlomiej WITKOWSKI (Warszawa, PL)
Cpc classification
H10F77/703
ELECTRICITY
C30B7/00
CHEMISTRY; METALLURGY
Y02E10/50
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
H10F10/164
ELECTRICITY
C23C16/407
CHEMISTRY; METALLURGY
H10F71/00
ELECTRICITY
H10F71/138
ELECTRICITY
International classification
H01L31/18
ELECTRICITY
Abstract
The invention relates to the photo-voltalic cell structure comprising semiconductor type-p substrate with bottom electric contact upon which the active ZnO film is present, with the transparent conductive layer upon it, preferably ZnO:Al film, with an electric contact, characterized in that the active ZnO layer consists of ZnO nanostructures film at least 50 nm thick, deposited on nucleating layer and covered with ZnO film at least 1 nm thick, and the method to produce the photovoltaic structure.
Claims
1. A photovoltaic cell structure, comprising semiconductor type-p substrate with bottom electric contact upon which the active ZnO film is present, with the transparent conductive layer upon it, preferably ZnO:Al film, with an electric contact, characterized in that the active ZnO layer consists of ZnO nanostructures film at least 50 nm thick, deposited on nucleating layer and covered with ZnO film at least 1 nm thick.
2. The structure according to claim 1, characterized in that the nucleating layer is a layer of gold, silver or ZnO, or nanoparticles of these materials.
3. The method of carrying out the photovoltaic cell structure, wherein upon p-type substrate with bottom electric contact an active layer of ZnO is deposited, upon which a transparent ZnO:Al electrode film and electric contact are deposited, characterized in that upon the substrate, preferably silicon, an active ZnO layer is created in the form of nanorods covered with ZnO film, wherein in order to produce that layer, the substrate is first covered with the nucleating layer, then the substrate with the nucleating layer is placed in a reaction mixture with pH of 6.5-12, containing a solvent, at least one oxygen precursor, and at least one zinc precursor, heated up to the temperature of 30-95 C. and kept in this temperature for at least 1 second, and after completion of this process, impurities are removed from the substrate and crystallized nanorods, preferably by annealing for at least 1 second in the temperature of 100 C., after which the nanorods are covered, in an ALD process, with ZnO film at least 1 nm thick, and so created active layer is covered with a transparent ZnO:Al electrode film, which the upper electric contact is made on.
4. The method of claim 3, characterized in that the nucleating layer is deposited on the substrate by cathode sputtering of gold, silver or nanoparticles of those metals.
5. The method of claim 3, characterized in that the nucleating layer is a ZnO layer or ZnO nanoparticles deposited on the substrate from a solution or obtained by annealing zinc salt deposited from a solution or deposited in at least 1 ALD cycle, whereing the zinc precursor is diethylzinc, dimethylzinc or zinc chloride, and the oxygen precursor is water, ozone or oxygen plasma.
6. The method of claim 3, characterized in that the oxygen precursor in the reaction mixture is water, and the zinc precursor is zinc acetate.
7. The method of claim 3, characterized in that the ZnO film that the nanorods of the active layer are covered with is deposited in at least 10 ALD cycles, using diethylzinc, dimethylzinc or zinc chloride as zinc precursor, and water, ozone or oxygen plasma as oxygen precursor.
8. The method of claim 3, characterized in that the transparent ZnO:Al electrode film is deposited in at least 100 ALD cycles with diethylzinc, dimethylzinc or zinc chloride as zinc precursor, water, ozone or oxygen plasma as oxygen precursor, and trimethylaluminum as aluminum precursor.
Description
[0003] The object of the invention is to develop a photovoltaic structure of increased efficiency and relatively cheap production method of such structure.
[0004] The first object of the invention is a photovoltaic structure comprising a p-type semiconductor substrate with bottom electric contact upon which the active ZnO film is present with the transparent conductive layer upon it, preferably ZnO:Al film with electric contact. In this structure, the active ZnO layer is placed between the substrate, preferably silicon, and the transparent conducting film layer, preferably ZnO:Al film. It is ZnO nanostructures layer at least 50 nm high, covered with ZnO film at least 1 nm thick. ZnO nanostructures are deposited on the nucleating layer, preferably gold, silver layer or on ZnO layer or on nanoparticles of those materials. Equally preferably, the transparent conducting layer is made of ITO (Indium tin oxide) or SnO.sub.2. ZnO nanostructures can have the form of nanorods.
[0005] The second object of the invention is the method of obtaining photovoltaic structure, characterized in that an active ZnO layer in the form of nanorods covered with ZnO film is made on a substrate, preferably silicon, with prepared bottom electric contact. In order to produce the active layer, the substrate is first covered with the nucleating layer. The nucleating layer can be a layer of gold, silver or nanoparticles of those metals deposited by means of cathode sputtering, or a ZnO layer or ZnO nanoparticles deposited from solution or obtained by zinc salt annealing (e.g. zinc acetate) deposited from solution or during at least 1 ALD cycle, where, as zinc precursor, diethylzinc, dimethylzinc or zinc chloride is used, and water, ozone or oxygen plasma as oxygen precursor. Upon depositing the nucleating layer, the substrate is placed in reaction mixture with pH of 6.5-12, containing a solvent, at least one oxygen precursor, and at least one zinc precursor, heated up to the temperature of 30-95 C. and kept in this temperature for at least 1 second. It is preferred when the oxygen precursor in the reaction mixture is water, and the zinc precursor is zinc acetate. Upon completion of the process, impurities are removed from the substrate and crystallized ZnO nanorods, preferably by annealing for at least 1 second in the temperature of 100 C., after which ZnO nanorods are covered with ZnO film in ALD process. Preferably, ZnO film is deposited in at least 10 ALD cycles with diethylzinc, dimethylzinc or zinc chloride as zinc precursor, and water, ozone or oxygen plasma as oxygen precursor. Further on, the active layer is covered with a transparent ZnO:Al electrode film, which the upper electric contact is made on. Preferably, the transparent ZnO electrode film with aluminum admixture is deposited in at least 100 ALD cycles with diethylzinc, dimethylzinc or zinc chloride as zinc precursor, and water, ozone or oxygen plasma as oxygen precursor, and trimethylaluminum as aluminum precursor.
[0006] The obtained structure generates electrical voltage when subjected to visible, infrared or near UV light spectrum. The technology of execution of photovoltaic structure according to this invention is cheap and simple, and the structure is a multiple use structure.
[0007] The invention will be explained in more detail with the Al/ZnO/ZnO.sub.NR/Si/Al photovoltaic structure embodiment illustrated in
[0008] To carry out the example structure, commercially available p-type silicon substrate with electrical resistivity of 2.3 cm and dimensions of 1.51.5 cm was used. First, the substrate was subjected to cleaning carried out in an ultrasonic cleaner. The substrate was cleaned in 3 steps of 30 seconds each, in isopropanol, acetone and deionized water consecutively. Upon the cleaned substrate 1, from the bottom, a film of aluminum 2, constituting the electric contact, was deposited with cathode sputtering. In the second step, the creation of the active ZnO layer in the form of ZnO nanorods 4 covered with thin film of ZnO 5 was commenced. For that purpose, first, silver nanoparticles constituting the nuclei 3 for hydrothermal growth of nanorods were deposited upon the upper surface of the substrate 1 also by cathode sputtering. Then, the substrate with the nuclei was placed in the reaction mixture containing dissolved zinc acetate brought to the pH value of 8. The mixture and the substrate were heated up to the temperature of 50 C. and the growth of nanorods to the height of 650 nm was continued in the temperature for 2 minutes. After the growth completed, the substrate 1 with the crystallized nanorods 4 was rinsed in isopropanol to remove possible impurities, and deposition of ZnO layer 5 upon them started. For that purpose, the substrate was placed in an ALD reactor where it was annealed for 2 minutes in 200 C. After annealing, the reactor chamber was cooled down to 160 C., in which temperature the ZnO nanorods (and the substrate in part) were thoroughly covered with ZnO film ca. 200 nm thick in 1000 ALD cycles. Next, without removing the substrate with the deposited active layer from the ALD reactor, the transparent electrode 6 film was deposited. At the same temperature (160) in 1700 ALD cycles, the active layer (nanorods 4 covered with ZnO layer 5) was covered with ZnO:Al film 300 nm thick, constituting the upper, transparent electrode 6. The electrode layer 6 was deposited using diethylzinc as zinc precursor, water as oxygen precursor, and trimethylaluminum as aluminum precursor. After depositing the electrode layer 6, the point ohmic contact to the ZnO:Al layer 7 made of aluminum was deposited by cathode sputtering process.
[0009] Covering the ZnO nanorods with the additional ZnO layer increased the area of the contact separating the carriers, which significantly increased the efficiency of the structure according to the invention. The obtained structure demonstrated the efficiency of 12.5% (laboratory measurements made with sunlight simulator)