FABRICATION METHOD OF SILICON NANONEEDLE ARRAY WITH ULTRA-HIGH ASPECT RATIO
20220267889 · 2022-08-25
Assignee
Inventors
- Xuecou TU (Nanjing, CN)
- Mengxin LIU (Nanjing, CN)
- Lin Kang (Nanjing, CN)
- Labao Zhang (Nanjing, CN)
- Xiaoqing JIA (Nanjing, CN)
- Qingyuan ZHAO (Nanjing, CN)
- Jian CHEN (Nanjing, CN)
- Peiheng Wu (Nanjing, CN)
Cpc classification
C23C14/022
CHEMISTRY; METALLURGY
C23C14/16
CHEMISTRY; METALLURGY
B82Y40/00
PERFORMING OPERATIONS; TRANSPORTING
International classification
C23C14/16
CHEMISTRY; METALLURGY
Abstract
A fabrication method of a silicon nanoneedle array with ultra-high aspect ratio includes the following steps: spin-coating two photoresist layers of methyl methacrylate (MMA) and polymethyl methacrylate (PMMA) A2 on a silicon substrate; subjecting the silicon substrate coated with the two photoresist layers of MMA and PMMA A2 to electron beam lithography to form a photoresist pattern on the silicon substrate; subjecting the silicon substrate on which the photoresist pattern is formed to electron beam evaporation (EBE) to deposit an Al film layer on the silicon substrate; subjecting the silicon substrate on which the Al film layer is deposited to stripping to obtain an Al film array deposited on the silicon substrate, which provides a mask for the subsequent inductively coupled plasma (ICP) etching process; and subjecting the silicon substrate covered with the Al mask to ICP silicon etching to obtain a silicon nanoneedle array structure.
Claims
1. A fabrication method of a silicon nanoneedle array with an ultra-high aspect ratio, comprising the following steps: step 1: spin-coating two photoresist layers of methyl methacrylate (MMA) and polymethyl methacrylate (PMMA) A2 on a silicon substrate; step 2: subjecting the silicon substrate coated with the two photoresist layers of MMA and PMMA A2 to an electron beam lithography to form a photoresist pattern on the silicon substrate; step 3: subjecting the silicon substrate formed with the photoresist pattern to an electron beam evaporation (EBE) to deposit an Al film layer on the silicon substrate; step 4: subjecting the silicon substrate deposited with the Al film layer to stripping to obtain an Al film array deposited on the silicon substrate for providing a mask for an inductively coupled plasma (ICP) etching process; step 5: subjecting the silicon substrate covered with the Al mask to the ICP silicon etching process to obtain the silicon nanoneedle array.
2. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein before spin-coating two photoresist layers of MMA and PMMA A2 on the silicon substrate, a pure silicon substrate is subjected to an ultrasonic cleaning for 5 min to 8 min successively with acetone, alcohol, and deionized water, and then blow-dried with a nitrogen gun to remove residual moisture on a surface.
3. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 1, the silicon substrate is first spin-coated with a layer of MMA and baked on a constant-temperature baking platform, and then spin-coated with a layer of PMMA A2 and baked.
4. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 2, the electron beam lithography only needs to be conducted once, and an exposure dose for the electron beam lithography is 750 μC/cm.sup.2.
5. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein the silicon substrate formed with the photoresist pattern obtained after the electron beam lithography is subjected to a development for 3 min in a solution of methyl isobutyl ketone (MIBK) and isopropyl alcohol (IPA) at a ratio of 1:3, then subjected to a fixation for 1 min in an IPA solution, soaked in deionized water for 10 s, taken out and blow-dried with a nitrogen gun to remove residual moisture on a surface, and subjected to the EBE to form the Al film layer.
6. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 3, a thickness of the Al film layer is controlled at 300 nm to 350 nm.
7. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 4, the silicon substrate deposited with the Al film layer is first immersed in an N-methylpyrrolidone (NMP) solution and heated in a water bath at 80° C. for 60 min, and then subjected to ultrasonic stripping in acetone, alcohol, and deionized water successively to finally obtain the Al film array deposited on the silicon substrate.
8. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 5, the ICP silicon etching process is conducted for 55 min at an air pressure of 20 mtorr, a temperature of 10° C., a radio frequency power of 20 W to 30 W, and an ICP power of 700 W to 900 W.
9. The fabrication method of the silicon nanoneedle array with the ultra-high aspect ratio according to claim 1, wherein in step 5, gases used for the ICP silicon etching process are SF.sub.6 and C.sub.4F.sub.8, wherein the SF.sub.6 has a flow rate of 32 Sccm and the C.sub.4F.sub.8 has a flow rate of 40 Sccm.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0013]
[0014]
[0015]
[0016]
[0017]
[0018]
[0019]
[0020]
[0021]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0022] The solution of the present disclosure will be further explained below in conjunction with accompanying drawings and specific examples.
[0023] The fabrication method of a silicon nanoneedle array with ultra-high aspect ratio according to the present disclosure mainly includes the following micro- and nano-processing steps:
[0024] (1) A pure silicon substrate is subjected to ultrasonic cleaning for 5 min to 8 min successively with acetone, alcohol, and deionized water, then blow-dried with a nitrogen gun to remove residual moisture on the surface, and then observed under an optical microscope to confirm that the surface is clean and has no obvious particles and debris. If the surface of the silicon substrate is not clean enough, the subsequent fabrication of a photoresist structure will be affected.
[0025] (2) The silicon substrate is spin-coated with a layer of MMA and then baked on a constant-temperature baking platform to remove residual moisture in the photoresist. Then the silicon substrate is spin-coated with a layer of PMMA A2 and baked in the same manner. According to a large number of experiments, parameters in Table 1 are preferred for the spin-coating and baking of MMA and PMMA A2. Under these parameters, the MMA and PMMA adhesive layers have a moderate thickness, prominent uniformity, and strong adhesion. The double-layer photoresist process used in this step can bring great convenience to the subsequent stripping step.
TABLE-US-00001 TABLE 1 EBL conditions Baking Pre-coating Main-coating temperature/ Photoresist r/min t1/s r/min t2/s time ° C./min MMA 600 5 3000 60 240/4 PMMAA2 600 5 3000 80 240/4
[0026] (3) The sample is subjected to electron beam lithography.
[0027] (4) A sample obtained after the electron beam lithography is subjected to development for 3 min in a solution of methyl isobutyl ketone (MIBK) and isopropyl alcohol (IPA) in a ratio of 1:3, then subjected to fixation for 1 min in an IPA solution, soaked in deionized water for 10 s, and blow-dried with a nitrogen gun to remove residual moisture on a surface. When a gas gun is used to blow-dry a sample, the gas output of the gas gun should not be too large, thereby avoiding the collapse of the photoresist pattern. Since both MMA and PMMA are positive photoresists, at the exposure dose in step (3), a circular pattern array area exposed by electron beam on the two photoresist layers will be removed after the development and fixation, and the remaining area unexposed by electron beam will be retained.
[0028] (5) An Al film layer with a thickness of 300 nm to 350 nm is deposited on a sample through EBE.
[0029] (6) A sample is first immersed in an N-methylpyrrolidone (NMP) solution and heated in a water bath at 80° C. for 60 min, and then placed in acetone, alcohol, and deionized water successively to strip the Al film deposited on the photoresist with an ultrasound machine to finally obtain the circular Al film deposited on the silicon substrate. When the stripping is conducted with the ultrasonic machine, a power should not be too high, thereby preventing the Al deposited on the silicon substrate from falling off.
[0030] (7) A sample covered with circular array Al masks is subjected to ICP silicon etching, and specific etching conditions include gas type, gas flow rate, ICP power, RF power, pressure, temperature, etching time, and the like. During etching, a thin silicon grease layer can be applied to the back of the sample to increase thermal conductivity.
[0031] The fabrication of a silicon nanoneedle can be divided into two parts as a whole: the fabrication of a tip structure at the top, and the fabrication of a columnar support structure below the tip. In ICP dry etching, different process parameters will lead to structures with different morphologies, and the present disclosure achieves the fabrication of a designed structure accordingly. In the ICP etching process used in the present disclosure, SF.sub.6 is used as an etching gas, and due to its isotropic etching characteristic showing in ICP dry etching, a proper proportion of C.sub.4F.sub.8 needs to be introduced for passivation.
[0032] Through a large number of process experiments, it can be known that a flow rate and a proportion of the etching gas show the most significant impact on the morphology of etching. Specifically, when a flow rate ratio of the etching gas to the passivation gas is small, an overall shape of a column appears to have a thin upper part and a thick lower part, and conversely, the overall shape appears to have a thick upper part and a thin lower part. Through a large number of experiments, four sets of stable and representative process parameters are summarized. Table 2 shows data of the four sets of process parameters. Images 1, 2, 3, and 4 in
TABLE-US-00002 TABLE 2 Influence of etching conditions on morphology Etching/passivation Design Etching Etching Bottom Top gas diameter time height diameter diameter No. Sccm/Sccm nm Overall morphology min μm nm nm 1 32/32 500 Thick upper part and 9 5 160 320 thin lower part 2 32/50 500 Thin upper part and 9 3.3 640 500 thick lower part 3 40/50 500 Uniform overall 9 4.6 476 465 4 40/40 200 Thick upper part and 9 4.5 60 126 thin lower part
[0033] (8) An etched sample is observed under a scanning electron microscope to determine morphology and measure key parameter information. According to results, process parameters are optimized. Through a large number of experiments, the present disclosure determines the optimal process conditions shown in Table 3.
TABLE-US-00003 TABLE 3 ICP etching conditions Gas flow ICP power RF power Pressure Temperature Etching time Gas rate Sccm W W mtorr ° C. min SF.sub.6 32 700-900 20-30 20 10 55 C.sub.4F.sub.8 40 (750 is the optimal) (20 is the optimal)