SRAM cell and its fabrication process

Active solid-state devices (e.g. – transistors – solid-state diode – Non-single crystal – or recrystallized – semiconductor... – Field effect device in non-single crystal – or...

Reexamination Certificate

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C257S057000, C257S350000, C257S393000, C257S903000

Reexamination Certificate

active

06204518

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to an SRAM (static random access memory) cell and its fabrication process. More particularly, the invention relates to an SRAM cell constituted in such a manner that a load device is a thin film transistor and that the SRAM cell is of a three-dimensional structure and high in integration density and operates at a low voltage, and also to its fabrication process.
2. Description of the Related Art
An SRAM cell is constituted from two inverters and two transfer transistors, wherein the two inverters are cross-connected and connected to bit lines by the two transfer transistors. The inverter is normally constituted from an NMOS driving transistor and a load device and applied with a supply voltage.
FIG. 4A
to
FIG. 4C
show typical SRAM cell structures. In
FIG. 4A
to
FIG. 4C
, three kinds of SRAM cells are shown; these SRAM cells differ in respect of the constitution and kind of a load device. Namely, in case of the SRAM cell shown in
FIG. 4A
, a resistor composed of PolySi is used as a load device
101
; in case of
FIG. 4B
, a transistor (called as a bulk transistor) formed on a substrate is used as the load device
101
; and in case of
FIG. 4C
, a transistor (called as a stacked transistor) formed on a driving transistor
103
is used as the load device
101
. Of these SRAM cells, the SRAM cells shown in FIG.
4
B and
FIG. 4C
are called as a full CMOS type SRAM cell, particularly, the SRAM cell shown in
FIG. 4B
is called as a bulk full CMOS type SRAM cell. Referring to
FIG. 4A
to
FIG. 4C
, reference numerals
102
and
104
denote a transfer transistor and a bit line, respectively.
In the above-described constitutions, in order to attain a higher integration density of the SRAM cell, the load devices
101
shown in
FIGS. 4A and C
are desirably a resistor composed of PolySi or a stacked transistor. This is because the load device
101
can be formed on the driving transistor
103
formed on the substrate, so that the element area can be reduced.
On the other hand, in view of driving the SRAM cell, the following is desired. In order to enhance the stability of the SRAM cell and drive it at a low voltage, the load device is required to be driven by a high current.
FIG. 5A
is a diagram showing the state of an SRAM cell. The robustness of the memory cell against unbalance, device mismatches and noise from power source and adjacent cells is characterized by the static noise margin: SNM. Graphically, the SNM is given by the side Vn=SNM of the maximum diagonal square Z formed between the transfer curves (X and Y) of both cell inverters. Further,
FIG. 5B
shows a relation between the load device transconductance &bgr;p and SNM. In
FIG. 5B
, it is shown that the higher the &bgr;p, the larger the SNM; and accordingly, a higher margin can be obtained.
Here, in case of the bulk full CMOS type SRAM cell shown in
FIG. 4B
, the &bgr;p of the load device
101
is usually so high as about 3×10
−5
A/V
2
. On the other hand, the &bgr;p of the load device
101
shown in
FIG. 4C
is usually about 1×10
−7
A/V
2
, so that in case that the supply voltage is 1 V or lower, it is difficult to make the bulk full CMOS type SRAM cell sufficiently operate. Further, in case of the bulk full CMOS type SRAM cell shown in
FIG. 4B
, the limit of the ON-state current of the load device
101
is 50 &mgr;A, but in case of the load device
101
shown in
FIG. 4C
, the limit of the ON-state current is 1 to 10 &mgr;A, and therefore, the cell can be used only at a high supply voltage.
Further,
FIG. 6
shows I-V characteristics of the load devices shown in
FIGS. 4A and C
. As is apparent from this
FIG. 6
, in case that a PMOS formed on the driving transistor is used as the load device, the cell can drive a large current and operate at a lower voltage.
Thus, in order that the cell operates stably in a high integration density and with a low voltage (1 V or lower), it is desired to use a load device composed of a stacked transistor at a driving current substantially the same as in a load device composed of a bulk transistor. For this reason, it is desired to improve the mobility of the stacked transistor.
In a stacked transistor, usually a PolySi film is used in an active region. For this reason, in order to improve a mobility of this transistor, it is required to increase the grain size (grain diameter) of a crystal constituting the PolySi film. As a method of increasing the grain size, there is known a method according to which a PolySi film is solid phase grown epitaxially from an amorphous Si film, for example by subjecting the film to a heat treatment at about 600° C. for about 30 hours or laser annealing.
However, the quality of the PolySi film obtained by this method is not sufficient for use in an SRAM cell. The reason for this, in case of this method, grain boundaries are scattered, so that the mobility is decreased, and at the same time, the characteristics of the SRAM cell are scattering. Further, since a long time and a high temperature are employed, the characteristics of the transistor formed on the substrate underneath the stacked transistor are deteriorated, this being also a problem.
As means for solving such problems, the following methods are exemplified.
As shown in
FIG. 7
, a portion of an insulation film
112
formed on a substrate
111
is bored to form an opening, and then, an amorphous Si film
113
is deposited and heat-treated, whereby a PolySi film is solid phase grown, with single crystal Si of the opening acting as a nucleus (Nobuhiko Oda, et al.,
Preprint of the
38
th Physics
-
Related Engineers Association in Spring of
1991, page 742 31p-X-12, “Solid Phase Growth of Si Using the U-LPCVD Method”). In
FIG. 7
, arrows indicate a direction of the solid phase growth.
As shown in
FIG. 8
, after a PolySi film
114
is deposited on a substrate
111
having a stepped portion, an Si ion
115
is implanted into the entire surface, to about the same thickness as in the PolySi film. By the Si ion implantation, the PolySi film
114
is converted into an amorphous state. But, since no Si ion is implanted into a PolySi film
114
a
existing in the side walls of the stepped portion, the PolySi film
114
a
remains in its polycrystalline state. Subsequently, by performing heat treatment, the PolySi film is solid phase grown, with the PolySi film
114
a
of the side walls acting as a nucleus (see Japanese Unexamined Patent Publication No. HEI 2(1990)-143414).
As shown in
FIG. 9
, after depositing an amorphous Si film on the substrate
111
having a stepped portion
116
, heat treatment is carried out to form an Si film
117
containing somewhat large polycrystals near the stepped portion. Next, the Si film portion, excepting the Si film existing near the stepped portion, which does not contain somewhat large polycrystals, is removed. Then, an amorphous Si film
118
is deposited over the entire surface, and heat treatment is carried out, whereby, with the somewhat large polycrystals acting as nuclei, a PolySi film having large grain boundaries is solid phase grown (see Japanese Unexamined Patent Publication No. HEI 8(1997)-288515). In
FIG. 9
, arrows indicate directions of the solid phase growth.
Besides the above-described methods, there is also known a method of forming a PolySi film by utilizing the fact that a catalytic element helps polycrystallization of amorphous Si (Japanese Unexamined Patent Publication No. HEI 9(1997)-312404). According to this method, first the catalytic element is contacted with a specific region of an amorphous Si film, and then, heat treatment is carried out, whereby, with the catalytic element acting as a nucleus, a PolySi film is solid phase grown. Next, by oxidizing the thus obtained PolySi film in an oxidizing atmosphere containing a halogen, an oxide film is formed on the PolySi film, and at the same time, the oxide film is subjected to gettering of the catalytic element. After this, by removing the oxide film, a PolySi film ha

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