The invention relates to a device and a method for the photo-voltaic generation of hydrogen from hydrogen-containing compounds, sunlight being concentrated on solar cells by means of an optical concentrator and the consequently generated voltage being used directly for the electrolysis of a hydrogen-containing compound, in particular of deionised water, in order to generate hydrogen.
Solar hydrogen can be obtained with the help of biological water splitting by bacteria, photoelectrochemical cells, from biomass reforming or by solar thermal splitting of water at high temperatures.
The electrolysis of hydrogen by means of photovoltaics has been achieved to date generally by separate, successively connected systems made of solar module and electrolysis unit. The same applies to systems which use wind energy for the electrolysis. Preliminary systems are described for example also in the review paper by M. A. K. Lodhi “A Hybrid System of Solar Photovoltaic, Thermal and Hydrogen: a Future Trend” Int. J. Hydrogen Energy, vol. 20, number 6, pp. 417-484 (1995). This publication also describes the use of concentrating PV systems for current generation and hybrid systems which both use solar-generated electricity and heat for the electrolysis.
The level of effectiveness of the hydrogen generation is relatively low for all these systems and the method is altogether expensive. In the past, there were also ideas of using solar cells directly for the electrolysis of water or an aqueous solution but the voltage of most solar cells at the operating point is too low to implement the electrolysis.
The electrolysis of water with the help of a semiconductor electrode was described for the first time in July 1972 in Nature vol. 238 “Electrochemical Photolysis of Water at a Semiconductor Electrode” by Akira Fijishima and Kenichi Honda. This publication shows how hydrogen can be separated from an aqueous solution with the help of sunlight. Water is hereby brought into direct contact with an n conducting semiconductor layer made of TiO2 and a Pt-counter-electrode. In the case of TiO2, the potential difference achieved in sunlight suffices for the splitting of water. It is described how hydrogen and oxygen can be obtained from water with this photoelectrochemical process. Because of the high band gap energy of TiO2 however, only a very small part of the solar spectrum is captured in the electrode and used for the electrolysis. Hence this process is not efficient.
In a patent by D. I. Tchernev from 1975 (U.S. Pat. No. 3,925,212) “Device for Solar Energy Conversion by Photo-Electrolytic Decomposition of Water”, it is shown for the first time that also separated p and n conducting semiconductor layers can be used as electrodes with illumination for splitting water. In this arrangement also there are semiconductor layers in direct contact with the electrolyte.
A further patent from 1984 “Photolytic production of hydrogen”, U.S. Pat. No. 4,466,869 by A. Williams, describes for the first time that the photoelectrode can also consist of a layer structure of a plurality of semiconductor layers which are mounted one above the other and have different band gap energy. Hence the photoelectrode corresponds in principle to a cascade solar cell, as is used also preferably in the invention described here. At the National Renewable Energy Laboratory NREL, work has taken place since 1998 on a system for the generation of hydrogen by means of solar energy. O. Khaselev, J. A. Turner describe in Science; vol. 280, Apr. 17 (1998), p. 425-427 “A Monolithic Photovoltaic-Photoelectrochemical Device for Hydrogen Production via Water Splitting” a photoelectrochemical method for water splitting. For the first time, a cascade solar cell made of III-V semiconductors was hereby used as one of the photoelectrodes. The counter-electrode consisted of platinum. In addition, the use of concentrated sunlight was mentioned for the first time. The semiconductor layers in all the mentioned arrangements are in direct contact with the electrolyte and themselves represent one of the electrodes for the water splitting. The photovoltaic energy generation and the electrolysis of water are hence not spatially separated.
It was therefore the object of the present invention to provide a system for the photovoltaic generation of hydrogen which has high efficiency in the hydrogen generation and thereby is simultaneously economical in production.
This object is solved by the device and the method for photo-voltaic generation of hydrogen according to claim 1 and 17. The further dependent claims reveal advantageous developments.
According to the invention, a device for the photovoltaic generation of hydrogen from hydrogen-containing compounds is provided, which consists of a plurality of units which track the position of the sun, which device has an optical concentrator for concentrating sunlight onto a solar cell, at least one solar cell which is not in contact with the hydrogen-containing compounds and is electrically connected to an electrolysis unit which has an anode and a cathode in contact with the hydrogen-containing compounds, the units being disposed on a tracking system following the position of the sun.
In comparison with systems known from prior art in which two separate systems are used, on the one hand, for photovoltaic current generation and, on the other hand, for electrolysis, the system underlying the present invention is characterised by the integration of solar power generation and hydrogen production in one system and hence by a lower material and spatial requirement, higher efficiency and potentially lower costs for the solar hydrogen. Hence electrical losses which are normally produced by the wiring of solar cells in a module are hence dispensed with. Even if individual cells within a module do not function, the functional capacity of the remaining units is not impaired. A substantial advantage relative to photoelectro-chemical methods is based on the fact that the photovoltaic cell is not in direct contact with the electrolyte. This can otherwise lead to significant problems, such as e.g. the oxidation of semi-conductor layers or the removal or deposition of material by the electrolysis. This extends the long term stability of such systems. In addition, optical absorption losses of the sunlight in the hydrogen-containing compound are avoided.
Preferably each individual unit of the device has an electrical power of 1 to 100 W.
The electrolysis unit according to the invention preferably has an operating temperature of −10° C. to 200° C., particularly preferred of 30° C. to 100° C.
A point-focusing lens, such as e.g. a Fresnel lens, is used preferably as optical concentrator. Alternatively, a curved Fresnel lens with a line focus, a parabolic mirror with a line focus or a dished mirror with a point focus can be used.
The solar cell is preferably constructed from a plurality of layers made of semiconductor materials which are connected to each other in series and have respectively different band gap energy. The semiconductor materials are thereby preferably selected from the group consisting of silicon, germanium and the III-V compounds of aluminium, gallium or indium with nitrogen, phosphorus, arsenic or antimony.
The polarity of the solar cell is freely selectable so that both an np polarity and a pn polarity is possible. The solar cell, if merely a pn or np transition is present, can have a voltage of more than 1.4 volts, particularly preferred of 1.6 to 2.4 volts. If the solar cell has a plurality of series-connected pn or np transitions, then a voltage in the range of 1.5 to 6 volts can be achieved. The solar cell thereby preferably has an area of 0.01 to 1 cm squared.
Preferably a proton-permeable polymer membrane (PEM) with two electrodes, the cathode and the anode is used as electrolysis unit.
Preferably the anode and the cathode consist of noble metals, in particular here platinum, palladium or iridium, the compounds thereof, e.g. iridium oxide, or of metals coated with noble metal, in particular here nickel, iron or copper. These materials also serve as catalyst for the electrolysis. The electrodes can preferably have in addition a distribution structure which is disposed on the electrodes in order to distribute the current. This is preferably a metal grating.
A further variant of the device according to the invention provides that the anode is connected to a channel system through which the hydrogen-containing compounds flow. The cathode is likewise connected to a channel system or to a gas-permeable material through which the generated hydrogen is discharged.
A further embodiment of the device according to the invention provides that the electrolysis unit consists of two or more units which are connected to each other in series and have a correspondingly higher operating voltage.
According to the invention, a method for the generation of hydrogen from hydrogen-containing compounds is also provided, in which sunlight is concentrated on at least one solar cell by means of an optical concentrator and, with the photovoltaically generated voltage, the hydrogen-containing compounds are electrolysed at a temperature preferably in the range of −10° C. to 200° C., particularly preferred of 30° C. to 100° C., the solar cell being contacted electrically with an electrolysis unit with a cathode and/or an anode and the protons formed by the electrolysis being conducted from the anode to the cathode where they are reduced to form molecular hydrogen.
A preferred embodiment of the method according to the invention provides that the hydrogen-containing compounds are also used for cooling in that the hydrogen-containing compounds are made to flow along the solar cell.
Preferably the hydrogen-containing compound contains deionised water in substantial parts. In this case, it is then also possible to generate also oxygen in addition to hydrogen.
The subject according to the invention is intended to be explained in more detail with reference to the subsequent Figures, without wishing to restrict said subject to the embodiments shown herein.
In
A first embodiment of a device according to the invention for the photovoltaic generation of hydrogen is illustrated in
The III-V materials have not been used for terrestrial energy generation to date since they are too expensive. By using concentrated light, the semiconductor surface is however significantly reduced and use becomes economical. In future, this is intended also to be used for solar power generation on earth. The Fraunhofer ISE has been working in this context for some years on the so-called FLATCON™ concentrator. This system likewise uses cascade solar cells with concentrated sunlight for the generation of electrical power.
In a cascade solar cell, a plurality of layers made of III-V semi-conductors of different band gap energy are deposited one on the other. These partial cells are monolithically, i.e. on the substrate, connected in series to each other. As a result, operating voltages between 1 volt for a single solar cell and approx. 6 volts for a solar cell with 5-6 series-connected pn transitions can be achieved. Solar cells with 3 pn transitions have achieved efficiencies of up to 37% for the conversion of concentrated sunlight into electrical energy (R. King et al. “Metamorphic III-V Materials” Proc. of 19th European Photovoltaic Solar Energy Conference Paris 2004). The combination of the band gaps and materials for the application described here must be reoptimised with respect to maximisation of the efficiency for the electrolysis of water. Examples of possible material combinations are for example GaInP/GaInAs, GaAs/Ge, AlGaInAs/Ge, AlGaAs/Si, GaInP/GaInAs/Ge, AlGaInP/GaAs/GaInNAs/Ge or AlGaInP/GaIn/AlGaInAs/GaInAsN/Ge. In addition to the lower consumption of materials, a further advantage in the use of concentrated light resides in the fact that the voltage of a solar cell increases logarithmically with the concentration.
The front and rear contact of the solar cell is connected directly via a metal grating 6 to electrodes (e.g. made of noble metals, such as platinum, palladium, iridium or iridium oxide which serve also as catalyst for the electrolysis, or made of nickel, iron or copper electrodes which are coated with such noble metals) on a proton-permeable polymer membrane (PEM) 4. The surface of the PEM membrane can extend up to the total surface of incidence of the sunlight (apart from the surface of the solar cell). The PEM membrane can however also adopt only a much smaller surface area. The membrane is on the positive side of the anode in direct contact with the hydrogen-containing solution which consists of e.g. deionised water 5. However other solutions can also be used which also need not necessarily be transparent. The solution will firstly flow through below the solar cells in one possible arrangement and contributes there to the cooling. As a result, the efficiency of the solar cells can be increased. Subsequently, the solution is conducted through a channel system to the anode and is split there into oxygen and hydrogen ions. The oxygen molecules produced on the anode side rise within the liquid and can be collected there. The H+ ions migrate through the PEM membrane to the negative cathode where they react with respectively two electrons to form molecular hydrogen. The cathode side is covered in turn with a channel system through which the hydrogen-containing solution flows or with a gas-permeable or porous material through which the hydrogen can be conducted to the store.
The principle of energy conversion is represented schematically in
In a further embodiment of the invention described here, two electrolysis units are connected in series. This is sensible if the voltage of the concentrator solar cell at the operating point achieves twice the voltage necessary for the electrolysis, i.e. approx. 3 volts. Such high voltages can be achieved with a single highly efficient cascade solar cell made of III-V semiconductors. A possible construction for the series connection of two PEM electrolysis units is shown in
In a further embodiment of the invention, respectively two to four concentrator solar cells are connected to only one electrolysis unit (see
Number | Date | Country | Kind |
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102004050638.8 | Oct 2004 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP05/10844 | 10/7/2005 | WO | 5/30/2007 |