Reference is made to and priority claimed from German application ser. no. 10 2005 028 901.0 filed on Jun. 17, 2005 and German application ser. no. 10 2005 051 573.8 filed Oct. 21, 2005.
The invention concerns an electronic device with a layer succession of the metal-insulator-metal or metal-insulator-semiconductor kind, in which the insulator layer contains praseodymium titanate.
Electronic devices with a layer succession of the kind metal-insulator-metal (MIM) or metal-insulator-semiconductor (MIS) are used for example as memory cells in memory devices such as DRAMs (dynamic random access memory) or as passive components in high-frequency applications.
Functionally, an MIM or an MIS structure, hereinafter also referred to in summarizing form for the sake of brevity as an MIM/MIS structure, forms a capacitor. A metal oxide semiconductor field effect transmitter (MOSFET) involves a layer succession of the metal-insulator-semiconductor kind, wherein the insulator layer performs the function of a gate insulator and the metal layer performs the function of a gate electrode. The semiconductor layer forms a channel for charge carriers between source and drain regions which are also arranged therein. Chip-integrated capacitors which self-evidently are used not only in memories but also in other electronic components are known both in the form of MIM and also MIS structures.
With the constantly progressing miniaturization of electronic devices, the dimensions of the MIM and MIS structures used therein have been so greatly reduced that the use of the insulator materials usually employed, silicon dioxide (SiO2) and silicon nitride (Si3N4), is becoming problematical; because the leakage current rises greatly because of the reduction in the SiO2 layer thicknesses.
Therefore in past years the search for insulator materials with an elevated dielectric constant (“high-k materials”) has been intensified. Replacement of the conventional materials SiO2 and Si3N4 by alternative dielectric high-k materials is intended primarily to reduce the area of the capacitor. Just recently a number of high-k materials such as Al2O3, AlTiOx, AlTaOx, (HfO2)1-x(Al2O3)x, HfO2, ZrO2, Y2O3, Tr2O5, PrTixOy and Pr2O3 were investigated as potential dielectrics for MIM/MIS capacitors. However, with the exception of Ta2O5, all those high-k materials have an excessively high positive square voltage capacitance coefficient (VCC, also identified by α). Therefore multi-layer dielectrics such as SiO2/HfO2 and Ta2O5/HfO2/Ta2O5 with very good VCC properties are discussed as alternatives. The capacitance density achieved hitherto is a maximum of 6 fF/μm2 for that layer stack.
The higher dielectric constant of alternative insulator materials means that it possible to achieve a greater capacitance density with the same area. Particularly promising candidates of such insulator materials are oxides of rare earths, including praseodymium oxide Pr2O3, see WO 02/13275.
In terms of the deposit of praseodymium oxide on silicon, it has proven to be advantageous to provide a thin praseodymium silicate intermediate layer which is of a maximum thickness of 5 nm. The praseodymium silicate is a mixed oxide containing silicon, praseodymium and oxygen, see WO 2004/032216 A1.
The use of praseodymium silicide as an electrode material is known, see WO 2004/006315 A2. The disadvantage of praseodymium silicide in relation to MIM/MIS uses is that it is a material which is not simple to integrate into highly developed CMOS process technologies. In particular high temperatures of around 800° C. are required for the deposit of praseodymium silicide, whereby damage can occur at devices already present on the same wafer.
The underlying technical object of the present invention is therefore that of providing an electronic device having an improved high-k MIM/MIS structure, which can be easily integrated from the process technology point of view.
In accordance with the invention that object is attained by an electronic device with a layer succession of the metal-insulator-metal or metal-insulator-semiconductor kind, in which the insulator layer of that layer succession contains praseodymium titanate or consists of praseodymium titanate and in which a metal layer of the layer succession or both metal layers of the layer succession contains or contain either titanium nitride TiNx, tantalum nitride TaN or ruthenium oxide RuO2 or a combination of at least two of said materials or consists or consist of one of said materials.
The alternative insulator material praseodymium titanate has the advantage over Pr2O3 of enhanced stability in relation to atmospheric influences. Praseodymium titanate is preferably used in the insulator layer in predominantly or completely amorphous form.
In accordance with the invention further a metal layer or both metal layers of the MIM layer succession contains or contain titanium nitride (TiNx, hereinafter also referred to for brevity representatively by the embodiment TiN) or tantalum nitride or ruthenium oxide. Alternatively the metal layer or both metal layers consists or consist completely of titanium nitride (TiN), tantalum nitride or ruthenium oxide.
The invention is based on the following realization. Metal electrodes for dual metal gate processes must have suitable work functions, that is to say work functions near the Si conduction band or the Si valence band edge for n- or p-MOSFETs. The change in work function between n+-polysilicon and p+-polysilicon is between 4.2 eV and 5.2 eV. It is possible to implement both n- and also p-MOSFETs by virtue of the choice of TaN (4.2 eV through 4.9 eV), TiNx (4.6 eV through 4.9 eV) or RuO2 (4.9 eV through 5.2 eV).
In addition the choice of the electrode material is determined by the permissible temperature budget of the process. The specified materials TiNx, TaN and RuO2 are suitable for deposit at low temperatures down to ambient temperature. That facilitates process implementation and avoids damage which is caused by a high thermal budget in terms of process implementation. In contrast to praseodymium silicide the specified materials are therefore easier to handle from the point of view of the process technology. TiN has a metallic conductivity with a specific electrical resistance of 11 μΩcm. The conductivities of TaN and RuO2 are in the range of between 50 and 250 μΩcm.
Preferred embodiments of the electronic device according to the invention are described hereinafter.
Irrespective of its structural properties praseodymium titanate can be present in the form Pr2Ti2O7 or in an alternative embodiment in the form Pr2-xTixO3.
In a further embodiment of the electronic device according to the invention the insulator layer contains a praseodymium titanate layer and an SiO2 layer which adjoins same and which in turn adjoins one of the metal layers or the semiconductor layer. The use of an SiO2 layer admittedly provides that the capacitance area density, that is to say the ratio of capacitance to area, is slightly reduced, but advantageously the voltage dependency of capacitance can be reduced in that way. An example of such a structure has a first metal electrode, an SiO2 layer adjoining same, a praseodymium titanate layer adjoining same and a second metal electrode adjoining same.
In a particularly preferred embodiment the layer succession on a silicone substrate has a titanium nitride layer, an SiO2 layer adjoining the titanium nitride layer, a Pr2Ti2O7 layer adjoining the SiO2 layer and a gold layer adjoining Pr2Ti2O7 layer. In this embodiment particularly high values in respect of capacitance density were achieved, wherein it is also possible with that structure at the same time to afford a low square voltage capacitance coefficient.
Favorable values of those two parameters can be achieved by a selection of the thicknesses of the SiO2 layer and the praseodymium titanate layer. Preferably the layer thickness of SiO2 layer is between 2 and 6 nm. Particularly good values of capacitance density and square voltage capacitance coefficient were achieved with a layer thickness of the SiO2 layer of 4 nm, in particular in combination with a layer thickness of the Pr2Ti2O7 layer of between 11 and 15 nm, preferably 13 nm.
In a further embodiment the electronic device is in the form of an MIS structure, that is to say it has a layer succession of the metal-insulator-semiconductor kind. In this embodiment the semiconductor layer preferably contains doped silicon or a doped silicon-bearing alloy such as silicon-germanium. The doping corresponds to the usual conductivity doping in electronic devices.
In a further embodiment the metal layer contains a mixture, that is to say besides titanium nitride (TiN) also tantalum nitride (TaN) or ruthenium oxide (RuO2). The advantages of TaN and RuO2 correspond to those of the TiN so that the technical object of the invention can also be achieved with a mixture of those materials.
For the production of an MIS structure with a silicon or a silicon-germanium (SiGe) electrode and an SiO2 layer which adjoins same and which forms a part of the insulator layer, no additional deposit step for the SiO2 layer is required in the production procedure because the natural SiO2 layer which is produced with contact with oxygen can be used. Instead of a pure silicon substrate it is also possible to employ a germanium-bearing Si substrate or a carbon-bearing SiGe-alloy.
A preferred configuration of the device according to the invention involves a capacitor structure. Preferably the capacitor structure has a layer succession of the metal-insulator-metal kind, wherein the metal layers form the capacitor electrodes and the insulator layer forms the capacitor dielectric.
In an alternative embodiment the electronic device can also be in the form of a MOSFET which includes a layer succession of the metal-insulator-semiconductor kind, wherein the insulator layer performs the function of a gate insulator and the metal layer performs the function of a gate electrode.
Further embodiments by way of example are described hereinafter with reference to the Figures in which:
In alternative embodiments the MIM structure 10 can contain either two capacitor electrodes of identical materials or of different materials. Instead of titanium nitride (TiN) the first capacitor electrode can also be made from tantalum nitride (TaN) or ruthenium oxide (RuO2). The same applies for the second capacitor electrode. The choice of the material is determined by the following points of view:
A sputtered TiN layer 34 is used as the lower electrode. An SiO2 layer 36 is formed thereon by gaseous phase deposition. A dielectric Pr2Ti2O7 layer 38 is deposited by vapor deposition of a Pr2O3/TiO2 mixture. Vapor-deposited Au layers are used as the upper electrode.
In series of tests, various MIM capacitors of that structure with different thicknesses of SiO2 layers and dielectric Pr2Ti2O7 layers were investigated. Some results of the investigation are set out hereinafter.
The illustrated configuration reflects the fact that C(V) curves of MIM capacitors with pure SiO2 are of a negative parabolic configuration while MIM capacitors with Pr2Ti2O7 as the dielectric exhibit positive voltage capacitance coefficients (VCC). A constant coefficient can therefore be achieved by a combination of the two dielectrics in a layered MIM structure. The low k value of SiO2 means that the resulting capacitance is reduced. Therefore the SiO2 layer should be kept as thin as possible.
Upon an increase in the thickness of the SiO2 layer 36 to 8 nm the sign of the voltage capacitance coefficient remains negative. The best VCC value achieved in a series of samples with identical Pr2Ti2O7 layer thicknesses as in the series in
The SiO2 layer also influence the leakage current properties as well as the breakdown voltage.
The operating voltage extrapolated to 10 years is 6 V in the case of MIM capacitors with 8 nm SiO2 and 24 nm Pr2Ti2O7 and 1 V in the case of capacitors with 4 nm SiO2 and 13 nm Pr2Ti2O7.
As a result layered high-performance SiO2/Pr2Ti2O7 MIM capacitors exhibit excellent electrical properties such as high capacitance densities, low voltage capacitance coefficients, high breakdown field strengths and a high level of reliability for the device.
Number | Date | Country | Kind |
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10 2005 028 901.0 | Jun 2005 | DE | national |
10 2005 051 573.8 | Oct 2005 | DE | national |