DETAILED DESCRIPTION OF THE INVENTION
[0015] Silicon-based field emitter tips, such as the micro field emitter tip shown in FIG. 1 , produce relatively high current densities under the influence of moderate electric fields and are relatively robust for lengthy periods of electronic emission. Silicon-based micro field emitter tips are, however, relatively expensive to fabricate. Conversely, thin-film field emission materials used in display devices, operation of which are illustrated in FIG. 3 , although relatively inexpensive to fabricate, currently appear to be less physically stable than silicon-based field emitter tips, and may produce lower current densities of emitted electrons for a given voltage. One aspect of the present invention is the recognition that these two different technologies can be combined in a dense field of tiny, silicon-based nano field emitter tips that can be fabricated across the surface of a silicon substrate. FIG. 4 illustrates a small region of the surface of a silicon substrate viewed with a dense field of tiny, silicon-based field emitter tips. In FIG. 4 , the nanofield emitter tips, such as nanofield emitter tip 402 , are shown having very regular sizes, geometries and interspacings, but such precision is not required to produce an effective flat field emission material. Large numbers of silicon-based nano field emitters may be irregularly shaped, defective, or missing without appreciably affecting the bulk emission characteristics of the surface of the silicon substrate.
[0016] A first embodiment of the present invention provides a relatively inexpensive method for producing tiny field emitter tips across the surface of a substrate material, including substrates, such as a silicon substrate, already containing microfabricated electronic circuits and microelectronic devices. FIGS. 5 A-D illustrate, in cross-section, a first method for fabricating tiny field emitter tips. In FIG. 5A, a substrate material 502 is first exposed to reactive ions, indicated in FIG. 5A by arrows, such as arrow 504 . The reactive ions are accelerated onto, or diffused into, a surface layer 506 of the substrate, forming covalent bonds with substrate atoms or molecules to produce nanoclusters within the surface layer having a chemical composition different from that of the substrate material. In FIG. 5A, a nanocluster is indicated by a small circle, such nanocluster 508 .
[0017] When the substrate material is silicon, a variety of different techniques can be used to produce reactive oxygen molecules, including ozone, oxygen-containing ions, or oxygen free radicals, and exposing the substrate material 502 with these active oxygen molecules, ions, or free radicals. These techniques include reactive ion etching (“RIE”) methods, electron cyclotron resonance (“ECR”) plasma generation, and downstream microwave oxygen plasma generation. Downstream microwave oxygen plasma generation is particularly attractive because it can be used to produce low-temperature oxygen free radicals, so that the silicon substrate need not be exposed to high temperatures during the process. The active oxygen molecules, ions, or free radicals combine with silicon atoms within the silicon substrate to produce SiO 2 molecules within the surface layer of the substrate. The SiO 2 molecules are produced by exposing the silicon substrate to the reactive oxygen molecules, ions, or free radicals to form tiny SiO 2 nanoclusters within the surface layer. The exposure conditions can be controlled to produce a desired density of SiO 2 nanoclusters. The depth of the surface layer of the silicon substrate in which the SiO 2 nanoclusters are generated may also be determined by controlling various RIE, ECR, or microwave plasma generation parameters such as the acceleration of the reactive oxygen species towards the silicon substrate, the temperature, plasma densities and ion fluxes, and other such parameters. Higher concentrations of SiO 2 nanoclusters result in smaller and thinner field emitter tips, and the length of the field emitter tips may be dependant on the depth of the surface layer of the silicon substrate in which SiO 2 nanoclusters are generated. Alternatively, reactive nitrogen molecules, ions, or other reactive species may be generated by analogous procedures to produce Si 3 N 4 nanoclusters within a surface layer of a silicon substrate. As yet another alternative, both reactive oxygen-containing and nitrogen-containing ions may be generated to produce various Si x O y N z nanoclusters, where the subscripts x, y, and z are determined by ion concentration ratios and other process parameters. Both SiO 2 and Si 3 N 4 are commonly used in dielectric insulating layers within finished semiconductor devices as well as for masks during silicon etching steps.
[0018] In a second step, in some cases optional, illustrated in FIG. 5 B, the silicon substrate may be thermally annealed using rapid thermal processing (“RTP”) technologies. The size and density of the nanoclusters within the surface layer 506 , produced in the first step, can be altered by heating and cooling the surface layer under controlled conditions. RTP parameters can be chosen to produce relatively regularly spaced nanoclusters of a desired size throughout the surface layer 506 . Nanoclusters 508 - 511 , produced by application of RTP to the substrate, are seen to be relatively regularly spaced and have approximately equal sizes. The sizes and spacing of the nanoclusters 508 - 511 determine the final sizes and spacings between field emitter tips.
[0019] In a third step, the substrate surface layer containing regularly sized and spaced nanoclusters is subjected to various different etch processes to remove substrate material not masked by the nanoclusters. FIG. 5C illustrates an intermediate stage of the etching process. As can be seen in FIG. 5 C, the nanoclusters, such as nanocluster 511 , serve as tiny, nascent-field-emitter-tip masks that block or inhibit etching of the substrate material below the nanoclusters. Thus, for example, the substrate material 512 below nanocluster 511 is a nascent field emitter tip, formed etching of adjoining substrate material not shielded from the etch medium by the nanocluster. In the case of SiO 2 or Si 3 N 4 nanoclusters within a silicon substrate, RIE etching may be employed using various different gas mixtures, including: (1) SiH 2 Cl 2 , O 2 and He or Ar; (2) NF 3 , SiF 4 , O 2 , and He; (3) HBr and Ar.
[0020] The third etching step may be continued until a final field of tiny field emitter tips is produced across the surface of the substrate. FIG. 5D illustrates a portion of a final field of tiny field emitter tips. In certain cases, continued etching eventually removes the nanocluster masks, so that no additional step is necessary. Alternatively, the etching may be discontinued prior to removal of the nanocluster masks, and the masks may be removed via a separate step, such as exposure of SiO 2 nanoclusters masks to a buffered oxide etch (“BOE”).
[0021] An alternative embodiment for producing tiny field emitter tips across the surface of a substrate material employs preferential etching of nanoclusters. FIGS. 6 A-C illustrate, in cross-section, a second method for fabricating tiny field emitter tips. In a first step, illustrated in FIG. 6A, a substrate material is exposed to, or bombarded with, reactive molecular, atomic, ionic, or free radical species to produce nanoclusters of a resulting covalent compound within the substrate, identical or similar to the first step in the first embodiment described with reference to FIGS. 5 A-D. Next, as illustrated in FIG. 6 B, the substrate is subjected to RTP in order to coalesce nanoclusters and uniformly disperse the coalesced nanoclusters throughout a surface layer of the substrate. This second step is identical to, or similar to, the second step of the first embodiment described with reference to FIG. 5B . However, the third step of the second method is quite different from the third step of the first embodiment. In the first embodiment, the nanoclusters serve as masks to protect substrate material below the nanoclusters from being etched by exposure of the substrate to an etch medium. In the second method, the substrate is exposed to an etch medium that selectively etches the nanoclusters, leaving nascent field emitter tips on the surface of the substrate separated by gaps resulting from selective removal of the nanoclusters. FIG. 6C illustrates nascent field emitter tips, such as nascent field emitter tip 602 , resulting from a selective etch of the nanoclusters formed in the first two steps illustrated in FIGS. 6 A-B. The selective etch also etches the substrate material, so that over time, the mesa-like field emitter tips are sharpened to produce a final field of tiny field emitter tips as illustrated in FIG. 5D . In the case of SiO 2 nanoclusters within a silicon substrate, freon-based plasma etch media, HF vapor etch media, and various wet etch solutions, including acetic acid and NH 4 F solutions, can be employed to selectively etch the SiO 2 . In the case of Si 3 N 4 nanoclusters, phosphoric acid wet etch solutions, CF 4 and freon-based plasma etch media, and other Si 3 N 4 selective etch media may be employed.
[0022] Silicon-based field emitter tips are also employed in various types of ultra-high density electronic data storage devices. FIG. 7 illustrates an ultra-high density electromechanical memory based on a phase-change storage medium. The ultra-high density electromechanical memory comprises an air-tight enclosure 702 in which a silicon-based field emitter tip array 704 is mounted, with the field emitter tips vertically oriented in FIG. 7 , perpendicular to lower surface (obscured in FIG. 7 ) of the silicon-based field emitter tip array 704 . A phase-change storage medium 706 is positioned below the field emitter tip array, movably mounted to a micromover 708 which is electronically controlled by externally generated signals to precisely position the phase-change storage medium 706 with respect to the field emitter tip array 704 . Small, regularly spaced regions of the surface of the phase-change storage medium 706 represent binary bits of memory, with each of two different solid states, or phases, of the phase-change storage medium 706 representing each of two different binary values. A relatively intense electron beam emitted from a field emitter tip can be used to briefly heat the area of the surface of the phase-change storage medium 706 corresponding to a bit to melt the phase-change storage medium underlying the surface. The melted phase-change storage medium may be allowed to cool relatively slowly, by relatively gradually decreasing the intensity of the electron beam to form a crystalline phase, or may be quickly cooled, quenching the melted phase-change storage medium to produce an amorphous phase. The phase of a region of the surface of the phase-change storage medium can be electronically sensed by directing a relatively low intensity electron beam from the field emitter tip onto the region and measuring secondary electron emission or electron backscattering from the region, the degree of secondary electron emission or electron backscattering dependent on the phase of the phase-change storage medium within the region. A partial vacuum is maintained within the air-tight enclosure 702 so that gas molecules do not interfere with emitted electron beams. Dense fields of tiny field emitter tips microfabricated according to the present invention are particularly suitable for application in these ultra high density electronic data storage devices.
[0023] Although the present invention has been described in terms of a particular embodiment, it is not intended that the invention be limited to this embodiment. Modifications within the spirit of the invention will be apparent to those skilled in the art. For example, it may be possible to introduce dissolved oxygen into the silicon in which the silicon substrate is cut during crystal growth in order to produce the higher densities of SiO 2 nanoclusters. As pointed out above, nanosilicon-based field emitter tips of various sizes and shapes can be produced by controlling the parameters of the ion exposure or ion implantation step, the annealing step, and the final SiO 2 etch step. Many different techniques well-known in microchip fabrication can be employed in each of the three steps. Dense fields of silicon-based nano field emitter tips can be prepared on thin silicon substrates that are affixed to the surface of microelectronic circuitry or, by contrast, fields of silicon-based nano field emitter tips can be directly fabricated on the surface of silicon-based microelectronic circuits. Field emitter tips can be fabricated on the surfaces of substrates other than silicon by choosing appropriate materials and method to produce nanoclusters within the substrate that can be etched, or that can mask an etch medium, selectively with respect to the substrate material. Finally, the present invention may be applied for fabrication of other types of silicon nanostructures, and may be generally applied to fabricating a wide variety of different types of nanostructures on the surface of different types of substrates.
[0024] The foregoing description, for purposes of explanation, used specific nomenclature to provide a thorough understanding of the invention. However, it will be apparent to one skilled in the art that the specific details are not required in order to practice the invention. The foregoing descriptions of specific embodiments of the present invention are presented for purpose of illustration and description. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed. Obviously, many modifications and variations are possible in view of the above teachings. The embodiments are shown and described in order to best explain the principles of the invention and its practical applications, to thereby enable others skilled in the art to best utilize the invention and various embodiments with various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents: