Method of fabrication of a ferro-electric capacitor and...

Details Method of fabrication of a ferro-electric capacitor and... Method of fabrication of a ferro-electric capacitor and...

2001-08-31

2003-04-08

Dinkins, Anthony (Department: 2831)

Electricity: electrical systems and devices

Electrostatic capacitors

Fixed capacitor

C361S303000, C361S305000, C257S295000, C257S296000

Reexamination Certificate

active

06545856

ABSTRACT:

FIELD OF THE INVENTION
The present invention is related to a method of fabrication of a ferro-electric capacitor.
The present invention is also related to a method of growing a PZT layer on a substrate.
The present invention is also related to a ferro-electric capacitor.
The present invention is related to a 3D-capacitor.
BACKGROUND OF THE PRESENT INVENTION
There is a development in the art of non-volatile memories based on ferro-electric capacitors (FERAM-structure). In this development PZT films are an important candidate material. Such PZT films are ferro-electric layers comprising at least platinum, zirconium and titanium. Usually they are in the form of: Pb(Zr, Ti) O
3
or (PbX) (Zr TiY) O
3
where X=La and Y=Ta, are in small concentration as dopants.
A ferro-electric PZT based capacitor is formed by sandwiching a PZT layer between a first and a second electrode, the first electrode being a bottom electrode, the second electrode being a top electrode.
The principal advantage of PZT materials is their relatively low (500-600° C.) crystallisation temperatures which are compatible with a base line CMOS process and their high remanent polarisation.
As the deposition of a PZT layer directly on a bottom electrode such as a Pt-layer leads to poor fatigue performance of the capacitor, it was suggested to have a conductive oxide layer first deposited on the Pt-layer before the deposition of the PZT layer. This conductive oxide can be a unary oxide having a rutile crystal structure such as IrO
2
, RuO
2
or OsO
2
or a complex oxide having a perovskite structure such as (La,Sr)CoO
3
.
For the synthesis of ferroelectric PZT layers, use is often made of a two-step process:
an amorphous layer is deposited, for instance by sol-gel or CVD or related techniques,
this amorphous layer is converted into a ferro-electric layer having a perovskite crystal structure by a thermal treatment (crystallisation).
While the growth of oriented PZT layers is in principal facilitated by the use of perovskite electrodes, unary oxides are in practice preferred because they are readily synthesised by reactive sputtering. RuO
2
has received the most attention in this respect because of its relatively low resistivity (50 &mgr;&OHgr;cm, the lowest of the rutile type oxides), excellent diffusion barrier properties, and proven compatibility with silicon technology.
In order to obtain PZT ferro-electric layers showing high quality hysteresis loops and ferro-electric switching properties, it may be advantageous to achieve a strongly preferential (111) orientation of the grains making up the PZT layer.
This goal can be achieved by using a template layer having a (111) orientation such as a sputtered Pt layer with the (111) orientation.
In order to achieve the desired (111) orientation in the PZT layer, a conductive oxide is commonly grown under conditions so as to obtain a columnar microstructure on top of the so-called template layer which has the property that it can be deposited with a strongly preferred orientation. In this type of microstructure there is a fixed orientational relationship between the grains of the Pt layer and the grains of the conductive oxide layer.
So in other words such conductive oxide layer with a columnar microstructure can transmit the orientation of the underlying Pt layer to thereby assure that the PZT layer formed on this conductive oxide layer will have, after crystallisation, the same orientation as the underlying PT layer. Because the grains of the Pt are strongly preferentially (111) oriented, this means that the grains of the conductive oxide layer will be preferentially oriented as well. Because the grains of the PZT layer grown subsequently will again tend to have a fixed orientational relationship with the conductive oxide, it is possible in this way to grow highly oriented PZT layers having a (111) orientation.
However, this conventional approach described here above has several drawbacks.
Firstly, the need to make use of a template layer such as Pt represents a considerable process complication. However the template layer is needed because without it, the conductive oxide has the property to grow with random or mixed structure.
Secondly, the columnar structure of both the first layer, i.e. the template layer and the second layer, i.e. the conductive oxide layer leads to inferior diffusion barrier properties of these layers. These diffusion barrier properties are necessary to protect the layers lying under the PZT layers against the indiffusion of oxygen during the growth of the PZT layer. This is of particular importance in a configuration where the bottom electrode of the capacitor is formed on a via connection, connecting said bottom electrode with the terminal of an active device, e.g. a MOSFET. This out-diffusion of oxygen can lead to a degradation of the electrical properties, particularly the conductivity, of this via connection.
Thirdly, the growth of a PZT layer on a bottom electrode with a columnar structure can have, depending on the application, a further disadvantage as it leads to PZT layers with small grain sizes, typically 100 to 200 nm lateral dimension. This small grain size is the result of the high nucleation rate of PZT on columnar layers during the crystallisation treatment. This high nucleation rate is due to the large surface roughness of columnar layers. This surface roughness is caused by the grains of the conductive oxide, which have the tendency to form facets. These facets form fixed angles with respect to the growth direction. Due to this effect, layers with smaller grains have a lower surface roughness. A higher surface roughness makes the formation of a nucleus with the desired crystal structure energetically favourable during crystallisation because the nucleation can take place in a recess at the surface between two adjacent grains thereby minimising the required amount of surface that needs to be created for formation of the nucleus. The small grained PZT layers obtained on columnar electrode layers renders the fabrication of ferro-electric devices on a single PZT grain impossible. Ferro-electric capacitors comprising a PZT layer being composed of a single grain are known to exhibit superior properties such as abrupt ferro-electric switching, low leakage current and high endurance compared to capacitors comprising multiple grains as such multiple grain capacitors incorporate grain boundaries.
Fourthly, fabrication of 3D capacitors using a columnar bottom electrode leads to an undesirable orientation of the PZT grown on the sidewalls. This misorientation implies that the purpose of 3D-capacitor fabrication, namely a gain in the amount of switchable charge per unit area on the wafer, is defeated. To avoid this problem, a new method has to be developed which does not employ the orientation of the bottom electrode grains as a means to control the orientation of the PZT grains.
AIMS OF THE INVENTION
The present invention aims to suggest a method of growing a PZT layer on a bottom electrode and accordingly a method of fabrication of a ferro-electric capacitor which do not have the drawbacks of the state of the art.
MAIN CHARACTERISTICS OF THE PRESENT INVENTION
According to a first aspect, the present invention is related to a method of fabricating a ferro-electric capacitor comprising the steps of:
creating a first electrode consisting essentially in a layer of a conductive oxide on a substrate,
forming a ferro-electric PZT layer on said conductive oxide layer,
creating a second electrode isolated from said first electrode on the top of the ferro-electric PZT layer,
wherein said conductive oxide layer comprises at least two sub-layers of individual grains, the top sub-layer having a random orientation of the individual grains.
Said conductive layer has a micro- or nano-crystalline structure. Preferably the conductive oxide layer has a grain size at least two times and preferably five times smaller than the conductive oxide layer thickness.
According to a first preferred embodiment said conductive layer is made of a unary oxide,

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