Deposition and chamber treatment methods

Coating processes – Direct application of electrical – magnetic – wave – or... – Plasma

Reexamination Certificate

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C427S255370, C427S255395, C427S333000, C427S343000, C427S344000, C427S402000, C427S569000

Reexamination Certificate

active

06589611

ABSTRACT:

TECHNICAL FIELD
The invention pertains to deposition and chamber treatment methods suitable for utilization in semiconductor fabrication processes. In particular aspects, the invention pertains to plasma utilization methods which can increase a ratio of processed wafers to plasma reaction chamber internal sidewall cleanings while maintaining low particle counts on the processed wafers. The invention also pertains to methods which can be utilized for silicon dioxide deposition during, for example, fabrication of shallow trench isolation regions.
BACKGROUND OF THE INVENTION
Plasma-enhanced deposition is commonly utilized during semiconductor fabrication for formation of various compositions. One type of plasma-enhanced deposition is high density plasma chemical vapor deposition (HDP-CVD). The plasma density utilized in an HDP-CVD process contains at least about 10
11
free electrons per cubic centimeter. Other plasma-enhanced deposition processes exist besides HDP-CVD, and the invention described herein can have application not only to HDP-CVD processes, but also to other plasma-enhanced deposition processes.
FIG. 1
illustrates an exemplary conventional apparatus
10
which can be utilized in a plasma-enhanced deposition process. Apparatus
10
includes a reaction chamber
12
comprising a sidewall
14
. An inlet port
16
extends through sidewall
14
, and an outlet port
18
extends across a bottom periphery of the shown chamber construction. Outlet port
18
has a valve
20
thereunder, and typically a pump would be provided to pull material from within chamber
12
when valve
20
is opened. Another valve (not shown) would typically be associated with inlet port
16
to enable the inlet port to be closed during various operations associated with chamber
12
.
A wafer holder
22
is shown within chamber
12
. Wafer holder
22
would typically be supported by various structures (not shown) to retain the holder in a desired location within chamber
12
.
A semiconductor wafer substrate
24
is illustrated supported by wafer holder (chuck)
22
. To aid in interpretation of the claims that follow, the terms “semiconductive substrate” and “semiconductor substrate” are defined to mean any construction comprising semiconductive material, including, but not limited to, bulk semiconductive materials such as a semiconductive wafer (either alone or in assemblies comprising other materials thereon), and semiconductive material layers (either alone or in assemblies comprising other materials). The term “substrate” refers to any supporting structure, including, but not limited to, the semiconductive substrates described above.
A plurality of coils
26
are shown extending around an upper region of chamber
12
. In operation, coils
26
are utilized to provide energy for maintaining a plasma within chamber
12
. Such plasma is illustrated diagrammatically as a cloud
28
in the illustration of FIG.
1
. Plasma
28
can be maintained through either inductive coupling or capacitive coupling relative to coils
26
.
Power sources
30
and
32
are shown coupled with coils
26
and wafer holder
22
, respectively. Power sources
30
and
32
can be utilized to provide power (such as, for example, radiofrequency power) to one or both of the inductive coils and the wafer holder. Although two power sources are illustrated, it is to be understood that a single power source can be utilized for providing power to both the coils and the substrate holder. In a deposition process, the power provided to holder
22
will be utilized to bias substrate
24
relative to plasma
28
so that species from the plasma will be drawn toward the substrate.
In a typical deposition process, one or more precursors are flowed through inlet
16
and utilized to form the deposit ultimately provided over a surface of substrate
24
. The precursors can comprise numerous materials, depending on the deposit that is ultimately desired to be formed. For instance, if the deposit is desired to comprise silicon dioxide, the precursors can include a source of silicon and a source of oxygen. The silicon source can, for example, comprise silane; and the oxygen source can, for example, comprise one or more of hydrogen peroxide, diatomic oxygen, and ozone. Alternatively, the silicon source can comprise tetraethylorthosilicate (TEOS).
As another example, if the deposit is to comprise silicon nitride and/or silicon oxynitride, precursors comprising silicon and one or more of nitrogen and oxygen can be flowed into the chamber. A suitable precursor of silicon is silane, and suitable precursors for one or both of oxygen and nitrogen include N
2
O, NH
3
, N
2
, O
2
.
A carrier gas can be provided to aid in flow of the precursors into chamber
12
, as well as to aid in maintaining plasma
28
. The carrier gas can comprise, for example, one or more of argon, helium and nitrogen.
FIG. 2
shows an expanded region of an upper left corner of reaction chamber
12
after a deposition process has commenced. A film
40
has formed along an internal surface of sidewall
14
. Film
40
is a by-product of the formation of a deposit within chamber
12
, and can comprise the same composition as the deposit formed on substrate
24
(FIG.
1
), or a different composition. The composition of film
40
includes materials from the precursors flowed into the reaction chamber. Accordingly, if the precursors comprise one or more of silane, oxygen and nitrogen, film
40
will typically comprise, consist essentially of, or consist of one or more of silicon, oxygen and nitrogen.
Material can flake from the film and fall onto a substrate (
24
of
FIG. 1
) within the reaction chamber to form particles across the substrate. The particles can cause numerous problems. For instance, the particles can be detrimental to chemical-mechanical polishing processes in that the particles can gouge a surface during the chemical-mechanical polishing. Also, the particles can be buried in subsequent process steps following a deposition process, and disrupt devices formed over the particles. Further, the particles can interfere with photolithographic processing.
Since particles resulting from flaking of material
40
are problematic, numerous procedures have been developed for removing material
40
from an internal sidewall of reaction chamber
14
. Such processes typically comprise cleaning an internal surface of the reaction chamber after a wafer is processed within the chamber.
An exemplary prior art process for depositing material on a wafer surface and cleaning a reaction chamber is described with reference to FIG.
3
. Initially, a wafer is placed within the reaction chamber. A deposit is then formed over the wafer surface, and the wafer is subsequently removed from the reaction chamber. After the wafer has been removed from the reaction chamber, interior sidewalls of the chamber are cleaned (typically a dry clean), and then the process can be repeated to treat another wafer. Accordingly, in typical prior art processes a single wafer is processed prior to cleaning internal sidewalls of a reaction chamber. It is noted that some chambers are configured to process a batch of two or more wafers. In such processes, material is deposited over the batch of wafers, and the batch is subsequently removed from the wafer prior to cleaning interior sidewalls of the chamber. In any event, typical prior art processes comprise providing a set of one or more wafers within a reaction chamber, forming a deposit over the set of wafers, and then cleaning interior sidewalls of the chamber before another set of wafers is processed.
The processing described above is typical for so-called cold wall chambers. Another type of chamber design is a so-called hot wall chamber. Hot wall chambers can have an internal periphery of a sidewall at a higher temperature than treated substrates, and such can reduce a rate of formation of a film along an internal periphery of the chamber relative to the rate of deposition of a material on a substrate. Accordingly, the time between cleanings of the chamber internal side

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