WO1981000487A1 - Hydrogen annealing process for silicon gate memory device - Google Patents
Hydrogen annealing process for silicon gate memory device Download PDFInfo
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- WO1981000487A1 WO1981000487A1 PCT/US1980/001020 US8001020W WO8100487A1 WO 1981000487 A1 WO1981000487 A1 WO 1981000487A1 US 8001020 W US8001020 W US 8001020W WO 8100487 A1 WO8100487 A1 WO 8100487A1
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- 239000001257 hydrogen Substances 0.000 title claims abstract description 34
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 31
- 238000000137 annealing Methods 0.000 title claims abstract description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims description 32
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims description 20
- 229910052710 silicon Inorganic materials 0.000 title claims description 20
- 239000010703 silicon Substances 0.000 title claims description 20
- 150000004767 nitrides Chemical class 0.000 claims abstract description 16
- 239000004065 semiconductor Substances 0.000 claims abstract description 9
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- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
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- 238000002955 isolation Methods 0.000 claims description 4
- 239000004020 conductor Substances 0.000 claims description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 abstract description 11
- 229920005591 polysilicon Polymers 0.000 abstract description 11
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- 230000014759 maintenance of location Effects 0.000 description 17
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- 239000007789 gas Substances 0.000 description 6
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 6
- KKEBXNMGHUCPEZ-UHFFFAOYSA-N 4-phenyl-1-(2-sulfanylethyl)imidazolidin-2-one Chemical compound N1C(=O)N(CCS)CC1C1=CC=CC=C1 KKEBXNMGHUCPEZ-UHFFFAOYSA-N 0.000 description 4
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- 238000010926 purge Methods 0.000 description 2
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/3003—Hydrogenation or deuterisation, e.g. using atomic hydrogen from a plasma
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B41/00—Electrically erasable-and-programmable ROM [EEPROM] devices comprising floating gates
Definitions
- This invention relates to processes for manu- facturing semiconductor non-volatile memory devices of the kind having a gate structure which includes a gate oxide layer provided on a semiconductor substrate, a nitride layer provided on said gate oxide layer and a polysilicon gate electrode overlying said nitride layer.
- SNOS silicon (polysilicon)-nitride-oxide- semiconductor.
- SONOS is silicon (polysilicon)-oxide-nitride- oxide-semiconductor.
- Gate oxide refers to the silicon oxide dielectric formed between the semiconductor and the silicon nitride (SNOS, SONOS) in the active area of a device such as a capacitor or field-effect transistor.
- Interfacial oxide refers to the silicon oxide layer formed between the polysilicon and the silicon nitride dielectric in SONOS structures. Retention and endurance are two very important characteristics of thin gate oxide, nitride non-volatile memory devices. Retention is a measure of the ability of the memory device to retain its stored charge sub ⁇ sequent to a write or erase operation. Endurance is a measure of the retention of the memory device as a function of the number of write-erase cycles to which the device has been subjected.
- High temperature processing is considered to be that at a temperature substantially higher than the nitride deposition temperature.
- the memory nitride which can be deposited at a temperature of about 700°C.-750°C. , is subjected to subsequent high temperature processing at, for example, 900°C. to 1000°C. , which degrades memory characteristics such as retention and endurance.
- This high temperature processing in ⁇ cludes for example, the high temperature (900°C.) phos ⁇ phorus diffusion step used in doping source, drain and polysilicon gates and oxidation of the polysilicon at 900°C.-1000°C. for generating masking oxide.
- silicon gate memory structures frequently have relatively low retention and endurance as compared to metal gate struc ⁇ tures (such as aluminum or aluminum alloy metal gate structures).
- metal gate struc ⁇ tures such as aluminum or aluminum alloy metal gate structures.
- the article relates to improved SONOS structures and discusses the relatively poor retention of silicon gate structures: for example, Chen indicated that 15 Angstrom thick gate oxide provides retention measured in years in typical MNOS structures, but only in hours in SONOS structures. Chen increased the retention of his SONOS devices by increasing the thickness of the gate oxide to 30 Angstroms. However increasing the gate oxide thickness has the disadvantage of slowing write and erase speeds.
- a process for manufacturing a semi ⁇ conductor non-volatile memory device of the kind speci ⁇ fied characterized by the steps of loading the device into an annealing vessel, raising the temperature of the vessel to within the range 600-1100°C. in hydrogen ambient, maintaining the temperature and hydrogen ambient for a sufficient time to anneal the device, and reducing the temperature of the vessel to about 100°C. or less while maintaining the hydrogen ambient.
- Fig. 1 is a cross-sectional representation of a silicon gate memory device which can be fabricated using the hydrogen anneal of the present invention.
- Fig. 2 is a schematic representation of apparatus for hydrogen annealing devices using the method of the present invention.
- Fig. 3 is a graphical represention of the retention and endurance characteristics of unannealed SONOS devices.
- Fig. 4 is a graphical representation of the retention and endurance characteristics of SONOS devices which have been hydrogen annealed using the method of the present invention.
- FIG. 1 A cross section of a fabricated n-channel SONOS memory trans ⁇ istor 10 is shown in Fig. 1.
- the difference between an SNOS device (not shown) and the illustrated SONOS device 10 is the absence in the SNOS device of the interfacial oxide layer 13.
- the invention will be described with reference to the SONOS device 10, keeping in mind that it is applicable to SNOS devices as well.
- the illustrated transistor 10 is formed by the well-known LOCOS (localized oxidation of silicon) process, although certainly the invention is not limited to this process.
- LOCOS localized oxidation of silicon
- source 17 and drain 18 are formed in ⁇ silicon substrate 16 by n-type impurities such as phosphorus (or p-type impurities such as boron for p-channel) using diffusion or ion implantation techniques.
- Field oxide 21 can be formed by wet thermal oxidation of the substrate 16, to a typical thickness of 14kA to 16kA (14,000 to 16,000 Angstroms).
- Memory gate oxide 11 of thickness 10-30 Angstroms is preferably formed by dry thermal oxidation, typically within the approximate range 600-750°C. in an oxygen-nitrogen ambient.
- the memory memory nitride 12 can be deposited by the chem- ical vapor deposition technique in a vertical reactor at a temperature of about 700-750°C. using an ammonia- silane-nitrogen ambient, to a thickness of about 350- 550 Angstroms.
- Interfacial oxide 13 may be formed by several methods, for example by high temperature (975°C.) wet oxygen thermal conversion of a portion of the top layer of the memory silicon nitride 12 to oxide 13. Inter ⁇ facial oxides 13 of 70-150 Angstroms thickness have been used.
- Polysilicon gate 14 can be deposited by either the atmospheric CVD (Chemical Vapor Deposition) or low pressure CVD technique over the temperature range
- Oxide isolation layer 22 is a low temperature ( 425°C) , deposited oxide 6kA° to 12kA° in thickness.
- the memory silicon nitride 12 is subjected to the high temperature ( 900°C.) phosphorus diffusion step used in doping source, drain and polysilicon gates.
- the nitride may also be subjected to a 1000°C. doped oxide reflow step in a nitrogen ambient.
- the SONOS transistor 10 is subjected to the hydrogen anneal of this invention, as described below, to enhance retention and endurance.
- the hydrogen anneal is performed after opening contact windows such as 35, 37 and 38, etc. in the oxide isolation layer 22 using standard photolithographic masking and etching techniques.
- contacts 25, 27 and 28 of material such as aluminum are formed using standard metallization techniques.
- a vertical reactor system 40 for practicing the hydrogen anneal of of the present invention.
- the system comprises a vessel such as a glass bell jar 41, a graphite suscep- tor 42 for holding the devices 10, cooling (water and rf heating coil) 43, and gas inlet tube 44.
- Gas here 2 and H 2
- the gas mixture and flow rate are controlled by valves 48, 49 and 51.
- Valves 48 and 49 can be used to control the relative proportions of hydrogen and nitrogen in the mixture, and valve 51 to control the gas flow rate.
- Gas flow rate is indicated by meter 52.
- a suitable hydrogen anneal process comprises: 1. loading the silicon gate trans ⁇ istor 10 onto the susceptor 42 of the reactor 40; 2. purging the reactor with nitrogen.
- OMPI WIPO e.g., for five minutes, typically at or near room temperature (valves 48 and 51 open; valve 49 closed) ;
- step 1 the loading step
- pre-condi ⁇ tion clean the bell jar 41 by heating to about 900°C. and maintaining the temperature for about 15 minutes in the presence of nitrogen (flow rates of about 48 liters/ min. have been used) , then shutting off the temperature and gas flow.
- the silicon wafer 16 from which the device is fabricated be in a 100% hydro ⁇ gen ambient when the temperature is raised from room temperature to the annealing temperature during step 4, and when the temperature is lowered from 800°C. during step 6 to avoid negating the beneficial effects of the hydrogen anneal.
- O PI V/IPO nealing vessel and system are not restricted to the particular vertical reactor 40 or to a vertical reactor at all: for example, a furnace tube (not shown) with suitable safety precautions should constitute a suitable annealing chamber.
- Figs. 3 and 4 The retention and endurance characteristics of unannealed SONOS devices and hydrogen-annealed SONOS devices 10 are shown in Figs. 3 and 4, respectively.
- the devices comprised the n- channel silicon gate field-effect transistors 10 de ⁇ scribed previously.
- the transistors were formed in accordance with the exemplary procedures described above.
- the substrate 16 was ⁇ 100> p-type, 15-20 ohm- cm silicon.
- the field oxide 21 was about 15kA thick as grown; oxide 22 was about 6kA thick.
- the approximate dimensions of the gate structure 15 are 10-15 Angstroms for the gate memory oxide 11; 500 Angstroms for the gate memory nitride 12; 70 Angstroms for the interfacial oxide 13; and 3.5kA for the polysilicon gate 14.
- annealed devices were annealed as described above in accordance with the principles of this invention.
- the anneal temperature was 800°C; the hydrogen flow rate was 48 liters/min. (steps 4, 5 and 6).
- the metallization was 14kA° thick aluminum. The parts were packaged in metal cans to facilitate handling and testing and avoid interaction with the ambient.
- the retention-endurance data of Figs. 3 (unannealed) and 4 (annealed) were obtained by: (1) initializing the FETs by determining the initial written (or "1") and erased (or "0") threshold voltages V ⁇ ; (2) generating uncycled retention-curves by storing the devices at an elevated temperature (125°C) for the times
- OMPI shown in Figs. 3 and 4 and determining the threshold voltages at intervals during this time; (3) write-erase cycling the FETs 10 times; (4) reinitializing the FETs per step 1; (5) and generating retention curves for the _ 5 - 10 cycles by again storing at elevated temperature per step 2.
- the initialization procedure (steps 1 and 4), i.e. obtaining the initial written and erased state threshold voltages, involved applying +25 volts for
- step 3 was done at room 5 temperature using an applied gate voltage of +_ 25 volts and a 10 millisecond pulse width for both polarities.
- the source, drain and substrate were all tied to ground during the write-erase cycling.
- the storage-at-temperature data for the 0 uncycled and cycled parts were obtained by first placing the packaged parts in an oven at 125°C. in an air ambient to accelerate charge decay. The parts were removed from the oven at various time intervals and the gate voltage (V tint) required for a 20 5 microamp drain-source current (I> DS ) was measured and recorded at room temperature.
- VERT gate voltage
- I> DS microamp drain-source current
- the absolute threshold voltage decay rates are sig ⁇ nificantly improved for the hydrogen annealed devices as compared to the non-annealed parts. More important ⁇ ly, the normalized threshold voltage window closure is lower for the hydrogen annealed parts than for the non- annealed parts.
- memory gate nitride layer 12 was deposited in a vertical reactor at atmospheric pressure, it is expected that the beneficial effects of hydrogen annealing should also be manifested by memory nitride layers deposited by other techniques, for example, low pressure CVD nitride layers.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
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- Insulated Gate Type Field-Effect Transistor (AREA)
- Non-Volatile Memory (AREA)
Abstract
In a method for manufacturing a semiconductor non-volatile SNOS or SONOS memory device having a gate structure which includes a gate oxide layer (11) provided on a semiconductor substrate (16), a nitride layer (12) provided on the gate oxide layer (11) and a polysilicon gate electrode (14) overlying the nitride layer (12), the device is annealed in hydrogen, in an annealing vessel (40), typically for 15-60 minutes at 600-1100 C.
Description
HYDROGEN ANNEALING PROCESS FOR SILICON GATE MEMORY DEVICE
Technical Field
This invention relates to processes for manu- facturing semiconductor non-volatile memory devices of the kind having a gate structure which includes a gate oxide layer provided on a semiconductor substrate, a nitride layer provided on said gate oxide layer and a polysilicon gate electrode overlying said nitride layer.
Background Art
Before discussing the background art, it is convenient to note the following four definitions of terms used in the present specification:
"SNOS" is silicon (polysilicon)-nitride-oxide- semiconductor.
"SONOS" is silicon (polysilicon)-oxide-nitride- oxide-semiconductor.
"Gate oxide" refers to the silicon oxide dielectric formed between the semiconductor and the silicon nitride (SNOS, SONOS) in the active area of a device such as a capacitor or field-effect transistor.
"Interfacial oxide" refers to the silicon oxide layer formed between the polysilicon and the silicon nitride dielectric in SONOS structures. Retention and endurance are two very important characteristics of thin gate oxide, nitride non-volatile memory devices. Retention is a measure of the ability of the memory device to retain its stored charge sub¬ sequent to a write or erase operation. Endurance is a measure of the retention of the memory device as a function of the number of write-erase cycles to which the device has been subjected.
In the fabrication of thin-oxide nitride non¬ volatile memory structures, it is important to keep the temperature of post-nitride deposition processing to a
OMPI
minimum, since high temperature processing of the memory oxide-nitride structure degrades the retention and endurance characteristics. High temperature processing is considered to be that at a temperature substantially higher than the nitride deposition temperature.
With respect to the fabrication of (n-channel) SNOS/SONOS silicon gate non-volatile memory devices, the memory nitride, which can be deposited at a temperature of about 700°C.-750°C. , is subjected to subsequent high temperature processing at, for example, 900°C. to 1000°C. , which degrades memory characteristics such as retention and endurance. This high temperature processing in¬ cludes for example, the high temperature (900°C.) phos¬ phorus diffusion step used in doping source, drain and polysilicon gates and oxidation of the polysilicon at 900°C.-1000°C. for generating masking oxide.
Because of this susceptibility to high tem¬ perature post-nitride deposition processing, silicon gate memory structures frequently have relatively low retention and endurance as compared to metal gate struc¬ tures (such as aluminum or aluminum alloy metal gate structures). This characteristic is discussed in an article by Peter C. Y. Chen entitled "Threshold-Alter¬ able Silicon Gate MOS Devices", IEEE Transactions on Electron Devices Vol. ED-24, No. 5, May, 1977, Page 584- 86. The article relates to improved SONOS structures and discusses the relatively poor retention of silicon gate structures: for example, Chen indicated that 15 Angstrom thick gate oxide provides retention measured in years in typical MNOS structures, but only in hours in SONOS structures. Chen increased the retention of his SONOS devices by increasing the thickness of the gate oxide to 30 Angstroms. However increasing the gate oxide thickness has the disadvantage of slowing write and erase speeds.
Disclosure of the Invention
It is an object of the present invention to
provide a process for manufacturing a semiconductor non¬ volatile memory device of the kind specified having improved retention and endurance (or, equivalently, a reduced rate of closure of the memory window) without unduly sacrificing other performance characteristics.
Therefore, according to the present invention, there is provided a process for manufacturing a semi¬ conductor non-volatile memory device of the kind speci¬ fied, characterized by the steps of loading the device into an annealing vessel, raising the temperature of the vessel to within the range 600-1100°C. in hydrogen ambient, maintaining the temperature and hydrogen ambient for a sufficient time to anneal the device, and reducing the temperature of the vessel to about 100°C. or less while maintaining the hydrogen ambient.
Brief Description of the Drawings
One embodiment of the invention will now be described by way of example with reference to the ac¬ companying drawings, in which: Fig. 1 is a cross-sectional representation of a silicon gate memory device which can be fabricated using the hydrogen anneal of the present invention.
Fig. 2 is a schematic representation of apparatus for hydrogen annealing devices using the method of the present invention.
Fig. 3 is a graphical represention of the retention and endurance characteristics of unannealed SONOS devices.
Fig. 4 is a graphical representation of the retention and endurance characteristics of SONOS devices which have been hydrogen annealed using the method of the present invention.
Best Mode for Carrying Out the Invention
Hydrogen annealing has been found to be effective in improving the memory characteristics of
both SNOS and SONOS memory device structures. A cross section of a fabricated n-channel SONOS memory trans¬ istor 10 is shown in Fig. 1. The difference between an SNOS device (not shown) and the illustrated SONOS device 10 is the absence in the SNOS device of the interfacial oxide layer 13. The invention will be described with reference to the SONOS device 10, keeping in mind that it is applicable to SNOS devices as well. Also, the illustrated transistor 10 is formed by the well-known LOCOS (localized oxidation of silicon) process, although certainly the invention is not limited to this process.
Typically, in forming the SONOS transistor 10, source 17 and drain 18 are formed in ρ~ silicon substrate 16 by n-type impurities such as phosphorus (or p-type impurities such as boron for p-channel) using diffusion or ion implantation techniques. Field oxide 21 can be formed by wet thermal oxidation of the substrate 16, to a typical thickness of 14kA to 16kA (14,000 to 16,000 Angstroms). Memory gate oxide 11 of thickness 10-30 Angstroms is preferably formed by dry thermal oxidation, typically within the approximate range 600-750°C. in an oxygen-nitrogen ambient. The memory memory nitride 12 can be deposited by the chem- ical vapor deposition technique in a vertical reactor at a temperature of about 700-750°C. using an ammonia- silane-nitrogen ambient, to a thickness of about 350- 550 Angstroms.
Interfacial oxide 13 may be formed by several methods, for example by high temperature (975°C.) wet oxygen thermal conversion of a portion of the top layer of the memory silicon nitride 12 to oxide 13. Inter¬ facial oxides 13 of 70-150 Angstroms thickness have been used. Polysilicon gate 14 can be deposited by either the atmospheric CVD (Chemical Vapor Deposition) or low pressure CVD technique over the temperature range
O
600-700°C. in SiH4- 2 and SiH4 ambients, respectively, to a thickness of 3kA-5kA. Oxide isolation layer 22 is a low temperature ( 425°C) , deposited oxide 6kA° to 12kA° in thickness. Subsequent to the polysilicon deposition, the memory silicon nitride 12 is subjected to the high temperature ( 900°C.) phosphorus diffusion step used in doping source, drain and polysilicon gates. Option¬ ally, the nitride may also be subjected to a 1000°C. doped oxide reflow step in a nitrogen ambient.
Subsequent to this high temperature proces¬ sing, the SONOS transistor 10 is subjected to the hydrogen anneal of this invention, as described below, to enhance retention and endurance. The hydrogen anneal is performed after opening contact windows such as 35, 37 and 38, etc. in the oxide isolation layer 22 using standard photolithographic masking and etching techniques. After the anneal, contacts 25, 27 and 28 of material such as aluminum are formed using standard metallization techniques.
Referring to Fig. 2 there is shown a vertical reactor system 40 for practicing the hydrogen anneal of of the present invention. The system comprises a vessel such as a glass bell jar 41, a graphite suscep- tor 42 for holding the devices 10, cooling (water and rf heating coil) 43, and gas inlet tube 44. Gas, here 2 and H2, is supplied via tube 44 to the vessel from pressurized sources such as tanks 46 and 47. The gas mixture and flow rate are controlled by valves 48, 49 and 51. Valves 48 and 49 can be used to control the relative proportions of hydrogen and nitrogen in the mixture, and valve 51 to control the gas flow rate. Gas flow rate is indicated by meter 52.
A suitable hydrogen anneal process comprises: 1. loading the silicon gate trans¬ istor 10 onto the susceptor 42 of the reactor 40; 2. purging the reactor with nitrogen.
OMPI WIPO
e.g., for five minutes, typically at or near room temperature (valves 48 and 51 open; valve 49 closed) ;
3. purging the reactor with hydrogen, e.g. , for, five minutes, typically at room tem¬ perature (valves 49 and 51 open; valve 48 closed);.
4. activating the rf coil 43 to raise the temperature of the reactor to the desired annealing temperature (within the approximate range 600-1100°C.) within a time span of about five minutes in the presence of hydrogen (valves 49 and 51 open; valve 48 closed) ;
5. maintaining the hydrogen flow and the temperature for a predetermined time (typi- cally within the range 15-60 minutes) to anneal the silicon gate transistor 10;
6. shutting off the rf coil 43 to allow the silicon gate transistor 10 to cool to the approximate range 24°C. (room temperature)- 100°C. in the hydrogen flow; and
7. terminating the hydrogen flow and removing the silicon gate transistor 10 from the reactor 40.
Although not critical, prior to step 1 (the loading step) it may be advantageous to pre-condi¬ tion (clean) the bell jar 41 by heating to about 900°C. and maintaining the temperature for about 15 minutes in the presence of nitrogen (flow rates of about 48 liters/ min. have been used) , then shutting off the temperature and gas flow.
It is important that the silicon wafer 16 from which the device is fabricated be in a 100% hydro¬ gen ambient when the temperature is raised from room temperature to the annealing temperature during step 4, and when the temperature is lowered from 800°C. during step 6 to avoid negating the beneficial effects of the hydrogen anneal. Finally, it is noted that the an-
O PI V/IPO
nealing vessel and system are not restricted to the particular vertical reactor 40 or to a vertical reactor at all: for example, a furnace tube (not shown) with suitable safety precautions should constitute a suitable annealing chamber.
Examples The retention and endurance characteristics of unannealed SONOS devices and hydrogen-annealed SONOS devices 10 are shown in Figs. 3 and 4, respectively. Referring again to Fig. 1, the devices comprised the n- channel silicon gate field-effect transistors 10 de¬ scribed previously. The transistors were formed in accordance with the exemplary procedures described above. The substrate 16 was <100> p-type, 15-20 ohm- cm silicon. The field oxide 21 was about 15kA thick as grown; oxide 22 was about 6kA thick. The approximate dimensions of the gate structure 15 are 10-15 Angstroms for the gate memory oxide 11; 500 Angstroms for the gate memory nitride 12; 70 Angstroms for the interfacial oxide 13; and 3.5kA for the polysilicon gate 14. After forming contact windows as needed in oxide 22, selected devices were annealed as described above in accordance with the principles of this invention. The anneal temperature was 800°C; the hydrogen flow rate was 48 liters/min. (steps 4, 5 and 6). Then, all samples, both annealed and unannealed, received metal contacts 25, 27, and 28. The metallization was 14kA° thick aluminum. The parts were packaged in metal cans to facilitate handling and testing and avoid interaction with the ambient.
The retention-endurance data of Figs. 3 (unannealed) and 4 (annealed) were obtained by: (1) initializing the FETs by determining the initial written (or "1") and erased (or "0") threshold voltages Vτ; (2) generating uncycled retention-curves by storing the devices at an elevated temperature (125°C) for the times
OMPI
shown in Figs. 3 and 4 and determining the threshold voltages at intervals during this time; (3) write-erase cycling the FETs 10 times; (4) reinitializing the FETs per step 1; (5) and generating retention curves for the _ 5 - 10 cycles by again storing at elevated temperature per step 2.
The initialization procedure (steps 1 and 4), i.e. obtaining the initial written and erased state threshold voltages, involved applying +25 volts for
10 three seconds and -25 volts for three seconds, respec¬ tively, at room temperature to the gates of the memory FETs. Source, drain and substrate were all tied to ground during this, initialization.
Write-erase cycling (step 3) was done at room 5 temperature using an applied gate voltage of +_ 25 volts and a 10 millisecond pulse width for both polarities. The source, drain and substrate were all tied to ground during the write-erase cycling.
The storage-at-temperature data for the 0 uncycled and cycled parts (steps 2 and 5) were obtained by first placing the packaged parts in an oven at 125°C. in an air ambient to accelerate charge decay. The parts were removed from the oven at various time intervals and the gate voltage (V„) required for a 20 5 microamp drain-source current (I>DS) was measured and recorded at room temperature. The decay of the stored charge, or equivalently, the rate of threshold voltage window closure as a function of log time for the unan¬ nealed and annealed SONOS transistors 10 is shown in 0 Figs. 3 and 4.
The main features of Figs. 3 and 4 are pre¬ sented in Table I.
OMPI
TABLE I
SONOS Retention, Endurance Characteristics
Hydrogen Write-Erase Window Window Window Decay Rate Normalized Window Anneal Cycles @1 hr, Wχ @100 hr, W2 ΔW=(W1-W2)/Decade Closure (Fig.) (Volts) (Volts) (Volts per Decade) ΔW/W-
No (Fig. 3) Uncycled 6.4 4 .0 1.2 0.19
1Q5 4.9 2. 3 1.3 0.26
Yes(Fig. 4) Uncycled 5.7 4. 5 0.6 0.11
105 6. 4 5. 1 0.65 0.10
The absolute threshold voltage decay rates are sig¬ nificantly improved for the hydrogen annealed devices as compared to the non-annealed parts. More important¬ ly, the normalized threshold voltage window closure is lower for the hydrogen annealed parts than for the non- annealed parts.
It has thus been shown that hydrogen anneal¬ ing of SNOS/SONOS process devices significantly im¬ proves retention and endurance. It is likely that the high temperature processing which the memory gate silicon nitride 12 is subjected to during the fabrica¬ tion of the memory structure 15 alters the physical and/or chemical characteristics of the silicon nitride in such a way as to degrade the memory characteristics. Annealing in a hydrogen ambient at least partially restores the memory device to its original memory characteristics.
Although the memory gate nitride layer 12 was deposited in a vertical reactor at atmospheric pressure, it is expected that the beneficial effects of hydrogen annealing should also be manifested by memory nitride layers deposited by other techniques, for example, low pressure CVD nitride layers.
Finally, it should be noted that the improved memory characteristics obtained with the pure memory SONOS transistors 10 should be equally valid for the split gate and trigate memory structures taught in U.S. Letters Patent No. 3,719,866 issued March 6, 1973 to Naber and Lockwood and assigned to NCR. Also, the im- proved memory characteristics are applicable to all silicon gate structures to which gate structure 15 is applicable, and includes capacitor structures as well as transistor structures.
O
Claims
1. A process for manufacturing a semicon¬ ductor non-volatile memory device having a gate struc¬ ture which includes a gate oxide layer (11) provided on a semiconductor substrate (16), a nitride layer (12) provided on said gate oxide layer (11), and a poly¬ silicon gate electrode (14) overlying said nitride layer (12), characterized by the steps of loading the device into an annealing vessel (40), raising the tem¬ perature of the vessel to within the range 600-1100°C. in hydrogen ambient, maintaining the temperature and hydrogen ambient for a sufficient time to anneal the device, and reducing the temperature of the vessel to about 100°C. or less while maintaining the hydrogen ambient.
2. A process according to clai 1, charac¬ terized in that said step of raising the temperature is effected within a time span of about five minutes.
3. A process according to claim 1, charac¬ terized in that the maintained temperature of the vessel (40) is about 800°C.
4. A process according to claim.3, charac¬ terized in that the temperature and hydrogen ambient are maintained for about 30 minutes.
5. A process according to claim 4, charac¬ terized in that said hydrogen ambient is provided at a flow rate of about 48 litres/minute.
6. A process according to claim 1, charac¬ terized in that prior to said step of loading the device into the annealing vessel (40), said vessel (40) is temporarily heated to about 900°C. in a nitrogen ambient for about 15 minutes.
7. A process according to claim 1, charac¬ terized in that subsequent to said step of loading the device into the annealing vessel (40) the vessel (40) is purged with nitrogen for about five minutes and then purged with hydrogen for about five minutes.
8. A process according to claim 1, charac¬ terized in that prior to said step of loading the device into the annealing vessel (40) , there are effected the steps of forming a thick isolation oxide layer (22) over the device and forming contact windows (35, 37, 38) in said thick isolation oxide layer.
9. A process according to claim 8, charac¬ terized in that after said step of reducing the tem¬ perature there is effected the step of forming a pat¬ terned conductor array (25, 27, 28) on the device.
10. A process according to claim 1, charac¬ terized in that said device is a SONOS device or a SNOS device.
OMP
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6580679A | 1979-08-13 | 1979-08-13 | |
US65806 | 1979-08-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1981000487A1 true WO1981000487A1 (en) | 1981-02-19 |
Family
ID=22065234
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1980/001020 WO1981000487A1 (en) | 1979-08-13 | 1980-08-07 | Hydrogen annealing process for silicon gate memory device |
Country Status (3)
Country | Link |
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EP (1) | EP0034168A4 (en) |
JP (1) | JPS56501028A (en) |
WO (1) | WO1981000487A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4448633A (en) * | 1982-11-29 | 1984-05-15 | United Technologies Corporation | Passivation of III-V semiconductor surfaces by plasma nitridation |
GB2229575A (en) * | 1989-03-22 | 1990-09-26 | Intel Corp | Method of reducing hot-electron degradation in semiconductor devices |
WO1991011022A1 (en) * | 1990-01-10 | 1991-07-25 | Australian Nuclear Science & Technology Organisation | Purification of semiconductor material |
US5229311A (en) * | 1989-03-22 | 1993-07-20 | Intel Corporation | Method of reducing hot-electron degradation in semiconductor devices |
EP0996148A1 (en) * | 1998-10-19 | 2000-04-26 | Matsushita Electronics Corporation | Method for fabricating semiconductor devices comprising a heat treatment step |
CN102800584A (en) * | 2012-08-29 | 2012-11-28 | 上海宏力半导体制造有限公司 | Method for improving reliability of SONOS flash memory |
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Cited By (8)
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US4448633A (en) * | 1982-11-29 | 1984-05-15 | United Technologies Corporation | Passivation of III-V semiconductor surfaces by plasma nitridation |
GB2229575A (en) * | 1989-03-22 | 1990-09-26 | Intel Corp | Method of reducing hot-electron degradation in semiconductor devices |
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US5229311A (en) * | 1989-03-22 | 1993-07-20 | Intel Corporation | Method of reducing hot-electron degradation in semiconductor devices |
WO1991011022A1 (en) * | 1990-01-10 | 1991-07-25 | Australian Nuclear Science & Technology Organisation | Purification of semiconductor material |
EP0996148A1 (en) * | 1998-10-19 | 2000-04-26 | Matsushita Electronics Corporation | Method for fabricating semiconductor devices comprising a heat treatment step |
US6316335B1 (en) | 1998-10-19 | 2001-11-13 | Matsushita Electric Industrial Co., Ltd. | Method for fabricating semiconductor device |
CN102800584A (en) * | 2012-08-29 | 2012-11-28 | 上海宏力半导体制造有限公司 | Method for improving reliability of SONOS flash memory |
Also Published As
Publication number | Publication date |
---|---|
EP0034168A4 (en) | 1981-12-10 |
JPS56501028A (en) | 1981-07-23 |
EP0034168A1 (en) | 1981-08-26 |
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