The invention refers to a method of depositing silicon onto a substrate by using a focused beam of charged particles, where a silicon-containing precursor is provided, which is being dissociated by the beam in direct proximity to the substrate. In addition, the invention refers to a corresponding device.
Methods of depositions, for example silicon depositions on a substrate (SiO2, AU etc.) have utility in many areas of microelectronics and related fields, but also in the areas directed to applied or basic research. Different methods are known for the deposition of materials (diamond layers, silicon-containing layers, tin oxide layers), for example chemical vapor phase deposition methods (CVD, Chemical vapor Deposition) or, also electron beam-based vapor deposition (EB-CVD, Electron Beam Chemical Vapor Deposition). The latter method is also termed as EBID (Electron Beam Induced Deposition or—when utilizing an ion beam as IBID (Ion Beam Deposition or IB-CVD). An additional normally used term for methods of this type is FPBID (Focused particle Beam Deposition).
During chemical vapor phase deposition, the substrate is normally heated to temperatures of several hundred degrees Celsius. From one or more of the reactants, solid components are deposited through chemical reactions from the vapor phase that are then deposited onto the substrate.
In the electron beam-based vapor deposition, a precursor is provided in direct proximity to the substrate, that is, essentially at its surface, from which by use of a focused electron beam, a solid component, for example silicon is deposited. Such a method could also be conducted through ion beams, which can be generated for example through a ion fine-jet installation.
With the two afore-described methods, deposition on the surface of the substrate can essentially be made for either two-dimensional or 3-dimensional structures.
From the article “Si deposition by electron beam induced surface reaction” by S. Matsui and M. Mito, Appl. Phys. Lett. 53 (16), 17 Oct. 1988, an electron beam-based vapor deposition method for the deposition of silicon on a substrate is known, where a silicon-containing precursor dichlorosilane (SiH2Cl2) is utilized. The depositions, according to the authors, contain 1.9 at-% chlorine.
The use of chlorine-containing precursors and in particular, SiH2CL2 has the drawback that the unintentional, but normally not avoidable inclusion of chlorine atoms in the deposition degrade the electrical properties of the deposition. In addition, the chlorine atoms can react with the aqueous portion of the residual vapor still residing in the reaction chamber, for example to form HCl and thus have a unintentional corrosive effect on the substrate and thereby damages the substrate. Furthermore, the free chlorine, due to its reactivity, can damage the deposition device itself (corrosion).
It is thus an aspect of the invention to provide a method for realizing a direct deposition of silicone on a substrate, which is especially effective and material-gentle and can be carried out in a precise manner. In addition, a device suitable for that purpose should also be provided.
Thus, with respect to the method according to the present invention, polysilicone is used as a precursor.
Further features of the present invention are the subject of the dependent claims.
The invention starts with the notion that the properties of silicone depositions on substrates have to be adapted to the increasing demands for modern applications. The demands refer in particular the conductivity, the structural size and the purity of the deposition. In addition, no damages or impurities should occur during the process of deposition.
To realize these demands, it is necessary that the silicone is directly deposited onto the substrate without the use of a lithographic mask technique. To this end, the silicone should be directly deposited by means of a particle beam induced dissociation of a precursor onto the substrate. In addition, a suitable precursor should be utilized in order to realize the highest quality of the silicone deposits. The precursor should be free of chlorine, since chlorine, due to its highly corrosive property, can damage the deposit and the substrate.
As has been now established, a precise, pure and gentle on the material silicone deposition is realized by utilizing a silicone containing precursor form the class of polysilanes, or a precursor containing polysilane. Polysilanes are free of chlorine, thus avoiding the corrosive effect of chlorine on the substrate and the deposit. Polysilanes also comprise chemical structures that can be precisely dissociated by a focused and charged particle beam and thus are able to realize a precise deposition of the silicone. The precursor molecules that are adsorbed at the surface of the substrate through different inelastic processes (i.e. “dissociative electron attachment”) are being dissociated into lasting and volatile components. The lasting components form the silicone deposit.
In a preferred embodiment of the method, the precursor neopentasilane (Si5H12) is utilized. Neopentasilane is free of chlorine, so that the highly corrosive effect of chlorine which occurs when using chlorine containing precursors is thus completely eliminated and at room temperature exhibits a vapor pressure favorable for the deposition process, preferably in the range of 0.1-100 mbar.
Further polysilanes that are utilized advantageously as precursors are cylic, branched and linear silanes (SinHm) to n=7, for example linear pentasilane (Si5H12) and linear hexasilane (Si6H14). These two polysilanes are free of chlorine, they are liquid at room temperature and at room temperature exhibit an advantageous vapor pressure for EBID/IBID methods.
An especially precise deposition, or a deposition with high spatial dissociation, in particular, in direction lateral to the substrate is realized by the use of an electron beam. In an alternative implementation of the method, the particle beam can consist of ions, for example Ga+-Ions. The use of such ion beams leads normally to a doping of the deposit.
In order to arrange localized deposits according to structural requirements on a substrate, the particle beam is advantageously moved for scanning across the deposit. Through the scanning and, preferably, the repeating motions across the substrate surface or across the already existing deposit, two-dimensional or three-dimensional structures can be created.
When using an electron beam, scanning of this type is advantageously created with the aid of a scanning electron microscope (SEM) for generating the electron beam. The lateral resolution of the method in this case is determined by the resolution capacity of the scanning electron microscope. Hereby, the exit area of the secondary electrons from the surface of the substrate in the surrounding of the beam focus must also be considered. At typical beam energies from 5 to 15 keV and currents around 100 pA, minimal structural widths of 10 to 20 nm or less are realized with high resolution microscopes. When using focused ion beams, scanning is preferably carried out with a scanning ion microscope. Thereby, structural sizes of 30 nm can be realized.
Providing or delivering the precursors to the surface of the substrate is carried out advantageously through a vapor injection system by which the precursor can be provided in target-directed manner in the area of the surface of the substrate, and where the deposit should be placed, which normally is the focus of the electron or ion beam.
Advantageously, the method is carried out at room temperature. The vapor pressure of neopentasilane at room temperature and of other, afore-stated polysilanes, are in a favorable range for FPBID processes. As a result, the deposition of silicon at room temperature is without any problems. Also, heating the substrate for the precursor is not necessary.
The method as described is advantageously applied to repair masks in lithographic processes. EUV masks (EUV=Extreme Ultra Violet) are prepared with electromagnetic radiation at wave lengths in the “distant” or extreme UV or X-ray range at 13.5 nm. Due to the very low transmission rate for the usual brand substrates, costly radiation treatments through the use of reflection is required. In order to compensate for the low reflectivity of single material layers at those wavelengths, multiple layers or multi-layered systems are used which function as Bragg's interferential mirror. According to the prior art, Mo—Si layer pairs are used that are repeated 40-50 times.
In this connection, a considerable problem lies already in the production of large surfaced mask structures that are free of defects. Defects can occur for example due to contamination from particles in the air, abrasion from manual systems or also the formation of crystals at the mask surface. The critical size of the defect is thereby below 30 nm, which is why only highest resolution corrective measures can work. A high resolution Si/MO—SI-EBID process can thus be advantageously applied not only in repairing masks that are already in use, but can be applied also on quality control and retro-improvements of already existing masks. The repair of Cr-based masks in conventional lithography at wave lengths in the range of 193 nm and ArF-excimer lasers as light source from EBID of Cr-based structures and electron beam-induced reactive etching is commercially applied for example by NaWoTec GmbH, an enterprise taken over by Carl Zeiss SMT AG.
The described method is advantageously carried out for editing of switching circuits. Further areas of application are in the areas directed to applied research and basic research.
With respect to the device, one of the aspects of the present invention is the use of a polysilane as a precursor. In a preferred variant of the device the precursor is a neopentasilane. Advantageously a scanning electron microscope is used as particle beam device.
The advantages that are realized with the present invention are in particular, the use of a silicone-containing precursor of the class of poly silanes in an EBID/IBID method, a direct deposition of silicone with high accuracy and resolution and few impurities. In particular, when using neopentasilane as a precursor, which at room temperature is in liquid form and which possesses a favorable vapor pressure for the EBID/IBID method, the silicone of great purity is easily deposited and without any inclusion of chlorine. With a guided (scanned or continuous) and repetitive motion of the particle beam across the substrate, a precise two-dimensional and three-dimensional deposit is produced.
An embodiment of the invention is shown in the drawings and is described in more detail. The very schematic illustration shows in:
Identical structures in all figures are designated with the same numerals.
The device 2 as illustrated in
In the present embodiment, neopentasilane (Si5H12) is used as precursor 20. Neopentasilane is carbon-free Si-precursor 20 which is liquid under ambient conditions. Upon disassociation of the precursor, a solid phase silicone is produced for deposited onto the substrate 32, and the volatile hydrogen-containing phase. At room temperature, the vapor pressure of neopentasilane is in a range favorable for FPBID-processes. Thus, growth rates of about at least 0.01 μm3/min are realized. In comparison to these values, the gaseous precursor SiH2Cl2 exhibits a much higher vapor pressure, so that it is expected that the adhesion coefficient is very low and the corresponding growth rate markedly lower than if neopentasilane were used.
Typical deposits that are realized with the device 2 consist of at least 87 at-% silicone, with portions of carbon (C) and oxygen (O) in the range of 5 to 7 at-%. This can be detected, for example, through the use of energy-dispersive X-ray analysis (EDX). The described impurities are the result of the residual gas compounds in the vacuum of the electron microscope during the described processes of the Si-deposition. These can be almost or completely eliminated by improving the vacuum.
In addition, with the device according to the present invention and the corresponding method, a deposition of silicone at a (moderately) heated (<100° C.) substrate is possible.
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Number | Date | Country | Kind |
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10 2010 0550564.9 | Dec 2010 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP11/06543 | 12/23/2011 | WO | 00 | 9/10/2013 |