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Showing posts with label CNTFETs. Show all posts
Showing posts with label CNTFETs. Show all posts

IBM Reveals Carbon Nanotube Based Field Effect Transistor Manufacturing Process


IBM has earned U. S. Patent 7,628,974 for its method to control single wall carbon   nanotube (SWNT) diameter growth during manufacturing by either chemical vapor deposition (CVD) or plasma enhanced chemical vapor deposition (PECVD).

Carbon nanotube based field effect transistors (CNTFETs) show great promise for device applications. Recently CNTFETs with excellent electrical characteristics comparable to state-of-the-art silicon MOSFETs have been demonstrated.  The electrical characteristics of CNTFETs however depends largely on the band-gap of the single wall carbon nanotube (SWNT) forming the channel of the transistor. Since the band-gap of SWNTs has a strong dependence on the diameter, accurate control of the diameter is essential to the success of any device technology based on carbon nanotubes.


A crucial difficulty in obtaining individual SWNTs by CVD is control of nanometric catalyst particle size at growth temperatures of 700-1000.degree. C. It has been theorized that the particle size of the growth catalyst used can define the diameter of as grown carbon nanotubes. This hypothesis has been supported by the observation that catalytic particles at the ends of CVD grown SWNT have sizes commensurate with the nanotube diameters Catalysts typically employed are transition metals, notably Fe, Mo, Co, NI, Ti, Cr, Ru, W, Mn, Re, Rh, Pd, V or alloys thereof. However, the synthesis of small catalyst particles with a narrow diameter distribution is complicated and difficult to control.

IBM controls the diameter of CVD or PECVD grown CNTs based on the control of the residence time of the gases in the reactor such as by controlling the pressure, or the gas flow rates, or a combination of both, independent of catalyst particle size, according to inventors Alfred Grill, Deborah Neumayer and Dinkar Singh.

The gas residence time is a measure of the average time of the gas in the reactor. Thus, if the flow is constant and the pressure increases, the residence time increases, and if the pressure is constant and the flow increases the residence time decreases. The inventors unexpectedly discovered that by varying the residence they can influence the nanotube diameter. If the residence time is too high, only pyrolytic carbon is deposited and if the residence time is too low, nothing is deposited. The residence time is typically about 1 minute to about 20 minutes and more typically about 1 to about 10 minutes. The residence time is typically determined by controlling the pressure, flow or both the pressure and flow in the reactor. By varying the residence time (e.g growth pressure and/or flow rates) of the CNT precursor gases in the CVD or PECVD reactor, nanotube diameter can be varied from about 0.2 nanometers to several nanometers to 100 nanometers.

FIGS. 1A-1B show scanning electron microscope images of CNTs grown at atmospheric pressure using identical catalysts, but different gas flows. (FIG. 1A shows that higher gas flow results in relatively thin tubes, while FIG. 1B shows that lower gas flows in result in relatively thick tubes).

 

A further aspect of the patent relates to fabricating a SWNT or array of SWNTs having well defined diameters and origins by the above disclosed processes wherein the SWNTs form the channel of a field effect transistor. A field-effect transistor having source and drain regions and a channel located between the source and drain regions is obtained by a process comprising: a) depositing a thin film of catalyst; b) lithographically patterning the thin film of catalyst to provide catalyst only in the source or drain region or both; c) removing unwanted catalyst from the channel region defined by the lithographic pattern; and d) growing nanotube with a well controlled diameter ranging from about 0.2 nanometers to about 100 nanometers by controlling the residence time of gases in the reactor used for the growing of the nanotube and wherein the channel region extends from the source region to the drain region.

IBM Controls SWNT Diameter Independent of Catalysts

IBM researchers Alfred Grill, Deborah Neumayer and Dinkar Singh have developed a process in which the diameter of carbon nanotubes grown by chemical vapor deposition (CVD) or plasma enhanced (PECVD) is controlled independent of the catalyst size by controlling the residence time of reactive gases in the reactor.

According to U.S. Patent Application 20090278114, IBM’s process offers a significant advantage in terms of catalyst preparation and the growth. When used in conjunction with a catalyst system with a narrow catalyst particle size, carbon nanotubes with a very narrow diameter distribution can be obtained. Also described in the application is a method for forming a novel structure comprising an array of CNTs with well defined diameters and lithographically defined origins. This structure is suitable for forming the channel region of CNT based FETs.

The gas residence time is a measure of the average time of the gas in the reactor. Thus, if the flow is constant and the pressure increases, the residence time increases, and if the pressure is constant and the flow increases the residence time decreases. The inventors “unexpectedly discovered” that by varying the residence they can influence the diameter of SWNT. If the residence time is too high, only pyrolytic carbon is deposited and if the residence time is too low, nothing is deposited. The residence time is typically about 1 minute to about 20 minutes and more typically about 1 to about 10 minutes. The residence time is typically determined by controlling the pressure, flow or both the pressure and flow in the reactor. By varying the residence time (e.g. growth pressure and/or flow rates) of the CNT precursor gases in the CVD or PECVD reactor, SWNT diameter can be varied from about 0.2 nanometers to several nanometers.

Since accurate size control of the catalyst particles is not required, a variety of catalyst systems deposited by a variety of solution deposition, or physical vapor deposition can be utilized for CNT growth. Suitable catalysts include the group of transition metals including Fe, Mo, Co, Ni, Ti, Cr, Ru, Mn, Re, Rh, Pd, V or alloys of them. The catalyst is then ramped up to the desired growth temperature in a suitable ambient prior to initiating carbon nanotube growth using a carbon containing precursor. The growth temperature is typically about 400 to about 1200.degree. C. and more typically about 500 to about 1000.degree. C.

Suitable carbon containing precursors include aliphatic hydrocarbons, aromatic hydrocarbons, carbonyls, halogenated hydrocarbons, silyated hydrocarbons, alcohols, ethers, aldehydes, ketones, acids, phenols, esters, amines, alkylnitrile, thioethers, cyanates, nitroalkyl, alkylnitrate, and/or mixtures. Other sources include methane, ethane, propane, butane, ethylene, acetylene, carbon monoxide, benzene and methylsilane. Other reactive gases such as hydrogen and ammonia, which play an important role in CNT growth, may also be introduced. Also, carrier gases such as argon, nitrogen and helium are used.

One of the main challenges facing carbon nanotube based electronics is the low drive currents of present-day CNTFETs. The low drive current stems from the extremely small diameter of SWNTs effectively resulting in a transistor with a narrow width. Using arrays of SWNTs for the channel region will increase the drive current, making CNTFET based technologies feasible. However, at the present time no controlled ways exist forming arrays of CNTs with a well defined pitch. Thus the ability to grow arrays of SWNTs with lithographically controlled origins (limited by ebeam resolution) and small diameters (<5 nanometers) is crucial to the success of CNT electronics. IBM’s discovery is a step towards carbon nanotube based electronics.
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