The present disclosure relates to the field of photovoltaic cells technologies, and more particularly, to a zinc magnesium oxide material, a method for producing the same and a solar cell.
Copper Indium Gallium Selenium (CIGS) thin film solar cells have characteristics of low pollution, no degradation, good weak light performance, and high photoelectric conversion rate. The CIGS thin film solar cell includes a buffer layer, the buffer layer always is cadmium sulfide (CdS). However Cd has toxicity and environmentally unfriendly, and thus cadmium-free buffer layer has become a new development direction, (Zn, Mg)O material can be used as one of the materials of cadmium-free buffer layer.
Some embodiments of the present disclosure provides a zinc magnesium oxide material, comprising at least two composite thin film layers, wherein, an atomic ratio of Zn element to Mg element in each of the at least two composite thin film layers is different from an atomic ratio of Zn element to Mg element in each of at least one remaining composite thin film layer of the at least two composite thin film layers.
In accordance with some embodiments of the present disclosure, the zinc magnesium oxide material is a composite material with a gradual changing optical band gap, and is a zinc magnesium oxide material with an adjustable optical band gap.
In accordance with some embodiments of the present disclosure, the atomic ratio of Zn element to Mg element ranges from 1:1 to 20:1.
In accordance with some embodiments of the present disclosure, along an incident direction of photons, atomic ratios of Zn element to Mg element in the at least two composite thin film layers gradually increase and band gaps of the at least two composite thin film layers gradually decrease.
In accordance with some embodiments of the present disclosure, the Zn element comes from a zinc-containing compound.
In accordance with some embodiments of the present disclosure, the zinc-containing compound is diethyl zinc.
In accordance with some embodiments of the present disclosure, the Mg element comes from a magnesium-containing compound.
In accordance with some embodiments of the present disclosure, the magnesium-containing compound is bis(cyclopentadienyl)magnesium.
Some embodiments of the present disclosure provides a method for producing the zinc magnesium oxide material, comprising: producing a ZnMgO material by using three precursors; and depositing at least two composite thin film layers on a substrate in sequence, wherein, atomic ratios of Zn element to Mg element in the at least two composite thin film layers gradually decrease along a direction away from the substrate.
In accordance with some embodiments of the present disclosure, before depositing the at least two composite thin film layers on the substrate in sequence, the method further comprises cleaning the substrate.
In accordance with some embodiments of the present disclosure, deposing the at least two composite thin film layers on the substrate in sequence comprises: placing the substrate on a sample tray and placing the sample tray in an atomic layer deposition apparatus; and setting a deposition temperature, and depositing the at least two composite thin film layers on the substrate in sequence under the deposition temperature.
In accordance with some embodiments of the present disclosure, the three precursors are diethyl zinc, bis(cyclopentadienyl)magnesium and water, respectively.
In accordance with some embodiments of the present disclosure, the deposition temperature ranges from 100° C. to 200° C.
In accordance with some embodiments of the present disclosure, the deposition temperature ranges from 105° C. to 135° C.
Some embodiments of the present disclosure provide a solar cell comprising a buffer layer, and the buffer layer comprises the aforementioned zinc magnesium oxide material.
The accompanying drawings described herein are used to provide further understanding to the disclosure and constitute a part of the disclosure. The exemplary embodiments of the disclosure and the description thereof are used to explain the disclosure, but do not constitute an improper limitation to the disclosure. In the accompanying drawings:
The technical solutions of the present disclosure will be described below in detail through embodiments. The following embodiments are only for illustration and explanation of the disclosure, but not for limitation to the disclosure.
Some embodiments of the present disclosure provide a buffer layer material used in a Copper Indium Gallium Selenium thin film solar cell. The buffer layer material is a zinc magnesium oxide (ZnMgO) material, and the zinc magnesium oxide material is a composite material with a gradual changing optical band gap. The optical band gap is defined as a photon energy corresponding to an absorption coefficient of 103 or 104 cm−1. The zinc magnesium oxide material is a thin film material composed of Zn element, Mg element, and O element, and the thin film material has a large width of forbidden band. Therefore, when the buffer layer material of the CIGS thin film battery is the zinc magnesium oxide material, visible light penetrates the buffer layer and reaches to an absorption layer, so that a quantum efficiency of the solar cell is increased.
In some embodiments of the present disclosure, the zinc magnesium oxide material includes two or more composite thin film layers, that is, at least two composite thin film layers.
In some embodiments of the present disclosure, the at least two composite thin film layers are produced with different atomic ratios of Zn element to Mg element. That is, the atomic ratio of Zn element to Mg element in each of the at least two composite thin film layers is different from an atomic ratio of Zn element to Mg element in each of at least one remaining composite thin film layer of the at least two composite thin film layers.
Exemplary, the zinc magnesium oxide material includes three composite thin film layers, and the atomic ratios of Zn element to Mg element in the composite thin film layers are 4:1, 6:1 and 9:1, respectively. Exemplary, the zinc magnesium oxide material includes four composite thin film layers, and the atomic ratios of Zn element to Mg element in the composite thin film layers are 4:1, 6:1, 7:1 and 9:1, respectively.
In some embodiments of the present disclosure, as shown in
The Zn element comes from a zinc-containing compound. In some embodiments of the present disclosure, the zinc-containing compound is dimethylzinc, zinc chloride, etc. In some other embodiments of the present disclosure, the zinc-containing compound is diethyl zinc. Since the diethyl zinc has a suitable saturated vapor pressure at a lower temperature, the diethyl zinc has a lower deposition temperature, thereby facilitating the deposition of the composite thin film layer.
The Mg element comes from a magnesium-containing compound. In some embodiments of the present disclosure, the magnesium-containing compound is bis(ethylcyclopentadienyl)magnesium (Mg(CpEt)2), etc. In some other embodiments of the present disclosure, the magnesium-containing compound is bis(cyclopentadienyl)magnesium. Since the bis(cyclopentadienyl)magnesium has a suitable saturated vapor pressure at a lower temperature, the bis(cyclopentadienyl)magnesium has a lower deposition temperature, and can be used to be performed an Atomic Layer Deposition (ALD).
A person skilled in the art can select the range of the atomic ratios of Zn element to Mg element according to actual needs. In some embodiments of the present disclosure, the atomic ratio of Zn element to Mg element ranges from 1:1 to 20:1, such as 1:1, 4:1, 6:1, 7:1, 9:1, 12:1, 15:1 or 20:1. When the atomic ratio of Zn element to Mg element is in the range of 1:1 to 20:1, the band gap of the composite thin film layer formed matches with that of each of other layers of the solar cell well. If contents of the Mg element in the composite thin film layer are small, the band gap of the zinc magnesium oxide material formed is small, thereby resulting in low open-circuit voltage (Voc) and efficiency of the battery. If contents of the Mg element in the composite thin film layer are large, the zinc magnesium oxide material formed will lose its semiconductor property and hinder the transmission of the photo-generated carriers, thereby resulting in significantly decline of the short-circuit current (Isc) and efficiency of the battery. It will be noted that the atomic ratios outside this range can also be used to produce the buffer layer material.
In some embodiments of the present disclosure, as shown in
Some embodiments of the present disclosure further provide a method for producing the zinc magnesium oxide material. As shown in
In some embodiments of the present disclosure, the three precursors are diethyl zinc, bis(cyclopentadienyl)magnesium and water, respectively.
In some embodiments of the present disclosure, the substrate is a glass.
In some embodiments of the present disclosure, before depositing the at least two composite thin film layers on the substrate in sequence, the method further includes cleaning the substrate.
In some embodiments of the present disclosure, depositing the at least two composite thin film layers on the substrate in sequence includes: placing the substrate on a sample tray and placing the sample tray in an atomic layer deposition apparatus. In addition, the method further includes: setting a deposition temperature, and depositing the at least two composite thin film layers on the substrate in sequence under the deposition temperature.
Exemplary, the method for producing the zinc magnesium oxide material includes steps 101-104 (S101-S104).
In step 101 (S101), a substrate is cleaned to obtain a cleaned substrate.
In step 102 (S102), a (Zn, Mg)O material is produced by using three precursors. Zn element comes from diethyl zinc, Mg element comes from bis(cyclopentadienyl)magnesium, and O element comes from water.
In step 103 (S103), the cleaned substrate is placed on a sample tray, the sample tray is placed in an atomic layer deposition apparatus, and a deposition temperature is set to deposit at least two composite thin film layers.
In step 104 (S104), the substrate on which the at least two composite thin film layers have been deposited is taken out.
In some embodiments of the present disclosure, the deposition temperature is in a range of 100° C. to 200° C.
In some embodiments of the present disclosure, the deposition temperature is in a range of 105° C. to 135° C. Such as 105° C., 110° C., 115° C., 120° C., 125° C., 130° C., 135° C.
In some embodiments of the present disclosure, as shown in
In step 1031 (S1031), an atomic layer deposition apparatus sprays a diethyl zinc steam once to a substrate on a sample tray, and then sprays water steam once, so that the diethyl zinc steam reacts with the water steam on the substrate and thus a first zinc oxide layer (with a thickness of one atomic layer in the thickness direction theoretically) is deposited. In turn, the above method for forming the zinc oxide layer is repeated eight times, and total nine zinc oxide layers are deposited on the substrate. Afterwards, the atomic layer deposition apparatus sprays the bis(cyclopentadienyl)magnesium steam once onto the ninth zinc oxide layers, and then sprays the water steam once, so that the bis(cyclopentadienyl)magnesium steam reacts with the water steam on the ninth zinc oxide layer and thus one magnesium oxide layer (with a thickness of one atomic layer in the thickness direction theoretically) is deposited. At this point, a first deposition of a first composite thin film layer is finished. The step 1031 is cyclically performed according to the target film thickness, and the preparation of the first composite thin film layer is finished. The atomic ratio of Zn element to Mg element in the first composite thin film layer is 9:1.
In step 1032 (S1032), according to the method for forming the zinc oxide layer in S1031, total six zinc oxide layers are deposited on the first composite thin film layer. Afterwards, the bis(cyclopentadienyl)magnesium steam is sprayed once on the sixth zinc oxide layer, and the water steam is sprayed once, so that the bis(cyclopentadienyl)magnesium steam reacts with the water steam on the ninth zinc oxide layer and thus one magnesium oxide layer is deposited. At this point, a first deposition of a second composite thin film layer is finished. The step 1032 is cyclically performed according to the target film thickness, and the preparation of the second composite thin film layer is finished. The atomic ratio of Zn element to Mg element in the second composite thin film layer is 6:1.
In step (S1033), according to the method for forming the zinc oxide layer in S1031, total four zinc oxide layers are deposited on the second composite thin film layer. Then the bis(cyclopentadienyl)magnesium steam is sprayed once on the fourth zinc oxide layer, and the water steam is sprayed once, so that the bis(cyclopentadienyl)magnesium steam reacts with the water steam on the ninth zinc oxide layer and thus one magnesium oxide layer is deposited. At this point, a first deposition of a third composite thin film layer is finished. The step 1033 is cyclically performed according to the target film thickness, and the preparation of the third composite thin film layer is finished. The atomic ratio of Zn element to Mg element in the third composite thin film layer is 4:1.
In some embodiments of the present disclosure, as shown in
After taking out the substrate on which the composite thin film layers have been deposited, morphology of the substrate is characterized by a Scanning Electron Microscope (SEM) to observe compactness and a surface morphology structure of the composite thin film layers. The atomic ratio of Zn to Mg in the substrate is detected by an Energy Dispersive Spectrometer (EDS), and the light transmittance of the composite thin film layers is tested by a spectrophotometer, so as to calculate the optical band gap of the composite thin film layers.
In some embodiments of the present disclosure, a multilayer composite film with different Zn/Mg atomic ratios is produced by adjusting the atomic ratio of Zn to Mg, and the multilayer composite film may realize continuous adjustment of optical band gap of the thin film.
Some embodiments of the present disclosure provide a solar cell. As shown in
The buffer layer and the absorbing layer in the solar cell form a pn junction, which is used as a working area of the thin film solar cell, so that the light energy is converted into electrical energy. Since the aforementioned zinc magnesium oxide material includes at least two composite thin film layers, and the atomic ratio of Zn element to Mg element in each of the at least two composite thin film layers is different from an atomic ratio of Zn element to Mg element in each of at least one remaining composite thin film layer in the at least two composite thin film layers, the buffer layer including the aforementioned zinc magnesium oxide material and the absorbing layer have a good match in energy band. Therefore, a good pn junction is formed, and the electrical leakage of the device is avoided. Therefore, the solar cell has a higher open circuit voltage, better fill factor and higher conversion efficiency.
Although some embodiments of the present disclosure have been shown and described, it will be apparent to those skilled in the art that various changes, modifications, amendments and variants can be made to these embodiments without departing from the principles and spirits of the present disclosure, and the scope of the disclosure is defined by the accompanying claims and their equivalents.
Number | Date | Country | Kind |
---|---|---|---|
201810090928.1 | Jan 2018 | CN | national |
This application is a national phase entry under 35 USC 371 of International patent Application No. PCT/CN2018/090297 filed on Jun. 7, 2018, which claims priority to Chinese Patent Application No. 201810090928.1, filed on Jan. 30, 2018, titled “A ZINC MAGNESIUM OXIDE MATERIAL WITH AN ADJUSTABLE OPEICAL BAND GAP, A METHOD FOR PRODUCING THE SAME AND A SOLAR CELL”, which is incorporated herein by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/CN2018/090297 | 6/7/2018 | WO | 00 |