This application claims priority to foreign French patent application No. FR 1003527, filed on Sep. 3, 2010, the disclosure of which is incorporated by reference in its entirety.
The field of the invention is that of components of integrated capacitor type comprising a dielectric layer between a top electrode and a bottom electrode and with a contact, necessitating the use of an electrical insulator between the two types of electrodes.
Typically, this type of component may be used within the context of piezoelectric actuators, notably for active optics or actuators for inkjet printers. Such components may also be used for producing resonators and acoustic radio-frequency filters that use a piezoelectric effect for mobile telephony. They are also advantageous for producing ferroelectric variable capacitors, very high value capacitors used for mobile telephony or mobile articles in general (pacemakers, communicating articles).
Currently, to produce planar technology integrated capacitors (referred to as MIM, for Metal Insulator Metal, capacitors), it is necessary to make the electrical contacts on the electrodes. Indeed, a typical structure of an MIM capacitor comprises a layer of dielectric known as functional dielectric DF sandwiched between two electrodes Es and Ei, the bottom electrode being on the surface of a substrate S covered with an insulating layer Ci as illustrated in
To make the contacts via a contacting layer RCsup and RCinf, and to avoid short-circuiting between the top and bottom electrodes, it is necessary to use an insulating dielectric DI as illustrated in
This insulating dielectric may be a silicon oxide SiO2 deposited by PECVD, by sputtering, or by spin-coating, commonly identified by the acronym “SOG” for “Spin-on Glass” for example. This may also be a silicon nitride SixNy deposited by PECVD, LPCVD for example, it could just as well be other insulating materials such as the following compounds: Ta2O5, Al2O3, MgO, AlN, etc.
One constraint for this insulating dielectric DI is that it must not disturb the operation of the functional dielectric DF. In particular, it is important that the capacitance that it adds in parallel to the device is negligible relative to the functional capacitance. In order to do this, the prior art uses an insulating dielectric DI of low dielectric constant relative to the functional dielectric DF.
For example, if the functional dielectric DF is Pb(Zr,Ti)O3 (PZT), the dielectric constant of which is typically equal to 1000, it is common to use a silicon oxide as insulating dielectric DI, the dielectric constant of which is equal to 4. Thus, the capacitance added by the SiO2 will be much lower than the capacitance of PZT, at a given equivalent surface area.
For PZT and other oxides having a very high permittivity, the use of the insulating dielectric DI may present a problem of reliability. Indeed, Bouyssou et al. (thesis of Emilien Bouyssou, p. 20, thesis of the University of Tours, 2006) observed that the SiO2 used as insulating dielectric DI is the cause of the appearance of brittleness in PZT capacitors, more precisely of a premature ageing of the capacitors in a constant voltage stress test. This is explained by the hydrogenated compounds used during CVD depositions of insulating dielectrics DI, the most commonly used method in the industry and notably illustrated in
Within this context, one subject of the present invention is a component of the integrated capacitor type using an electrically insulating dielectric that does not have the aforementioned drawbacks and for which the manufacturing process proves to be particularly advantageous.
More specifically, one subject of the present invention is an integrated capacitor comprising a layer of dielectric material known as functional dielectric material based on crystallized material of perovskite type, between at least one first electrode known as a bottom electrode at the surface of a substrate and at least one second electrode known as a top electrode, said electrodes being electrically insulated by a layer of electrically insulating material in order to allow at least one contact on the top electrode, characterized in that:
According to one variant of the invention, the electrically insulating material is placed on or under the top electrode.
According to one variant of the invention, the crystallized functional dielectric material is an oxide from among the following oxides: Pb(Sr,Ti)O3, SrTiO3, (Ba,Sr)TiO3, (Pb,La)(Zr,Ti)O3, Pb(Mg,Nb,Ti)O3, Pb(Zn,Nb,Ti)O3, BiFeO3, BaTiO3.
According to one variant of the invention, the amorphous electrically insulating dielectric material is an oxide from among the following oxides: PZT, SrTiO3, (Ba,Sr)TiO3, (Pb,La)(Zr,Ti)O3, Pb(Mg,Nb,Ti)O3, Pb(Zn,Nb,Ti)O3, BiFeO3, BaTiO3.
According to one variant of the invention, the functional and electrically insulating dielectric materials have the same chemical composition.
According to one variant of the invention, the electrodes are made of platinum or of ruthenium, or of ruthenium oxide, or of iridium, or of iridium oxide, or of gold.
According to one variant of the invention, the substrate is made of silicon and comprises an upper oxide layer.
According to one variant of the invention, the capacitor also comprises an adhesion layer between the substrate and the bottom electrode layer.
Another subject of the invention is a process for manufacturing an integrated capacitor according to the invention, characterized in that it comprises at least one step of producing a layer of amorphous and electrically insulating dielectric material, on top of or underneath the top electrode, via a sol-gel process comprising:
According to one variant of the invention, the process comprises at least:
According to one variant of the invention, the crystallization is carried out by rapid thermal annealing (RTA).
Thus, the present invention notably advantageously proposes to use a process of sol-gel type in a method which may appear to be a “degraded” method that does not give crystallized layers for the amorphous material, since the implementation of the latter stops after the calcination step, without implementing the crystallization step, which requires an annealing operation at higher temperature.
The invention will be better understood and other advantages will appear on reading the following description given non-limitingly and owing to the appended figures, among which:
steps 6a to 6k illustrate the various steps of a process for manufacturing an integrated capacitor according to the invention.
According to the invention, it is proposed to use a sol-gel process that makes it possible to produce components having a high permittivity dielectric layer and a layer of material having a lower permittivity providing an electrically insulating role between the two types of electrodes known as bottom and top electrodes.
In the case of very high permittivity materials, a well-known technique is the sol-gel process and notably of sol-gel polymerization type. The sol-gel deposition of PbTiO3 (PT) was reported for the first time in 1984 by G
The following year, Budd et al., B
The principle of the sol-gel process is based on a succession of hydrolysis-condensation reactions, at a temperature close to ambient temperature, which results in the formation of an inorganic polymer, which may then be heat treated. The step of hydrolysing metal alkoxides is shown schematically by the following reaction:
M-OR+H2O→M-OH+ROH
where M is a metal cation, and R an alkyl organic group. This reaction allows the conversion of the alkoxy functions to hydroxyl functions. The solution obtained is called a sol; that is to say a solid phase, constituted of small entities, dispersed in a liquid (the solvent). The hydroxyl functions are then converted to M-O-M species corresponding to the formation of an inorganic macromolecular network constituting the gel. This takes place following several condensation reactions (formation of oxo, —O—, bridges by oxolation) reactions, with removal of alcohol and of water.
M-OH+M-OR→M-O-M+ROH
M-OH+M-OH→M-O-M+H2O
The production of piezoelectric films via the sol-gel technique consists of a succession of steps of spreading the sol-gel solution and of heat treatments. For example, a succession of steps of spreading of sol-gel, drying (at 100° C.-150° C.), pyrolosis (at 300° C.-500° C.), and crystallization (at 600° C.-800° C.).
The solution is customarily spread over a substrate by spin-coating. The film thickness deposited depends mainly on the speed of rotation of the spin coater and on the physicochemical parameters of the solution (viscosity, concentration, evaporation rate). A drying step makes it possible to evaporate a portion of the solvents and to obtain a solid deposit. The layer then undergoes a pyrolysis (or calcination) in order to remove the organic residue.
This step, generally carried out on a hotplate, is crucial since it considerably conditions the structural quality of the piezoelectric film. The calcination temperature must be high enough in order to remove all of the organic residue (typically between 300° C. and 450° C.). Otherwise, the trapping of organic matter may lead to the presence of porosities. However, too high a temperature risks promoting the appearance of a parasitic phase, such as pyrochlore in the case of PZ, described in the publication: G
After pyrolysis, the amorphous layer obtained is crystallized and densified at a temperature between 600° C. and 800° C. This crystallization step is usually carried out by rapid thermal annealing (RTA), rather than by conventional annealing, in order, notably, to limit the thermal budget. The rapid thermal annealing (RTA) process is today among the most-used processes for the crystallization of thin films. Its main asset is a transmission of thermal energy via radiation and not by convection. This results in extremely rapid temperature rises which may reach up to 300° C./s owing to the use of halogen lamps. The annealing operations last a few tens of seconds. The thickness of a layer after crystallization is generally around 50 nm. Depending on the final material thickness desired, it is necessary to repeat all of the steps described previously several times. However, the crystallization step is very often carried out every two or three layers pyrolysed. The advantage of using the RTA process in order to reduce both the thermal budget and the manufacturing time of the films is then understood.
The sol-gel process has the advantage of being inexpensive and relatively simple to implement, requiring only a spreading area, hotplates and an RTA furnace. Furthermore, it does not require significant maintenance, which is a considerable asset compared to vacuum deposition techniques. It is furthermore very flexible for the development of complex materials. It is thus possible to easily vary the compositions by means of metering the organometallic precursors, or else to incorporate dopants in order to optimize the properties of the films.
Generally, the material deposited by the sol-gel process undergoes several steps. After pyrolysis, the material has been stripped of all its organic compounds (therefore H and C). The resulting material is therefore exclusively composed of non-organic materials after this pyrolysis (sometimes called calcination). As the material is not crystallized, it does not have a very high dielectric constant.
The present invention proposes to exploit this property of lower dielectric constant in order to use this layer referred to as a calcined or pyrolysed layer, as an insulating dielectric DI as illustrated in
The integrated capacitor according to the invention comprises, in this example, a functional dielectric material of perovskite type having a high dielectric constant, which may notably be PZT, and an electrical insulator of dielectric type of amorphous perovskite type, which has not undergone a final crystallization annealing phase, between the bottom electrode and the top electrode, as illustrated in
The various steps of the process are described below with the aid of
In order to produce such a multilayer, it is possible to use a silicon substrate S0, typically 200 mm in diameter. An oxidation step is carried out that defines a surface layer S1 of SiO2 having a thickness of 500 nm, as illustrated in
An adhesion layer Cac is then deposited by sputtering of 5 nm of titanium Ti followed by an oxidation, by rapid thermal annealing, of 2 minutes at 750° C. under oxygen O2. This adhesion layer may also be made of tantalum Ta.
The bottom electrode Ei as illustrated in
The functional dielectric made of PZT is then prepared via the sol-gel process as mentioned in the reaction scheme described previously, which is referenced DFcris and is illustrated in
A final crystallization annealing operation is then carried out at 700° C. in air for 30 seconds. Generally, this annealing should be carried out every 3 PZT deposition/drying/pyrolysis operations.
It is possible to use materials other than PZT, having a very high permittivity, which may notably be one of the following oxides: SrTiO3, (Ba,Sr)TiO3, (Pb,La)(Zr,Ti)O3, Pb(Mg,Nb,Ti)O3, Pb(Zn,Nb,Ti)O3, BiFeO3, BaTiO3.
The PZT is then etched by a wet etching process based on the following preparation: HF at 1%, HCl at 37% in water and in the following relative proportions: 5/9/50. This etching may also be carried out by dry etching using RIE (Reactive Ion Etching) equipment with gases of chlorinated type with addition of argon as illustrated in
The top electrode Es made of Pt and having a thickness typically of 100 nm, as illustrated in
The insulating dielectric, referenced DIam, and illustrated in
This insulating dielectric is then etched by a wet etching process based on the preparation: 1% HF-37% HCl—H2O in the proportions 5/9/200. This etching is defined using, prior to the etching, a photoresist defined by a photolithography step using a dedicated mask as illustrated in
A metal is then deposited to make the contact Rc as illustrated in
This layer is then etched by a wet or dry etching process as illustrated in
Finally, a protective insulating layer I as illustrated in
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