Abstract

We have explored the direct use of anodized alumina (AAO) fabricated on an Si wafer as a mold for the nanoimprint lithography (NIL). The AAO mold has been fabricated over more than 10 cm2 area with two different pore diameters of  nm and  nm. One of the key challenges of the lack of bonding between the antisticking self-assembled monolayer (SAM) and the AAO has been overcome by modifying the surface chemistry of the fabricated AAO mold by coating it with thin SiO2 layer. Then we have applied the commonly used silane-based self-assembled monolayer (SAM) on these SiO2-coated AAO molds and achieved successful imprinting of resist pillars with feature size of  nm by using the mold with a pore diameter of  nm. Finally, we have achieved (001) oriented L10 FePt patterned structure with a dot diameter of  nm by using a AAO mold with a pore diameter of  nm. The perpendicular Hc of the unpatterned and patterned FePt is about 3.3 kOe and 12 kOe, respectively. These results indicate that AAO mold can potentially be used in NIL for fabricating patterned nanostructures over large area.

1. Introduction

Nanoimprint lithography (NIL) has attracted enormous attentions [16] of the nanofabrication community since its innovation in 1995 [7] and regarded as a next generation nanofabrication tool for fabricating sub-10 nm features [35]. The NIL is a high-throughput and low-cost lithographic technique that showed its potential in many emerging fields, such as electronics [8], photonics [9], bit-patterned media [10, 11], and biological applications [12]. Bit patterned media is of particular interest due its potential in increasing the areal densities in magnetic data storage devices [13, 14]. The mold (also known as template or stamp) is the crucial part of the NIL that determines the throughput and resolution of the later in practical applications. Usually electron beam lithography or focused ion beam lithography followed by the pattern transfer using reactive ion etching (RIE) are used for making the mold. The high cost and low throughput of these methods limit the usefulness of the NIL for fabricating nanopatterns over large area for both of the research and practical applications. Therefore, exploring the fabrication of low-cost and highly robust large-area mold is a must to enjoy the full potential of the NIL. However, to date, only very few works have been reported in this highly demanding area. Park et al. [15] fabricated the large-area mold by using block-copolymer lithography that involved an extra-pattern transfer step. Kim et al. [2] and Lee et al. [16] used AAO membrane filled with carbon and aluminum, respectively, that also involved number of harsh steps, like fabrication of AAO membrane that is difficult to handle due to its brittle nature, attaching that AAO membrane with another rigid substrate, deposition of carbon or aluminum, heat treatment, ion milling, and chemical etching.

In this paper, we have demonstrated the direct use of AAO fabricated on an Si wafer as the mold by modifying the surface chemistry of the AAO mold by coating it with a thin SiO2 layer using atomic layer deposition (ALD). We have successfully fabricated FePt nanostructure with  nm feature size over 1 cm2 area. Our developed mold is highly economic, and both of the lateral and vertical dimensions can be controlled easily [17, 18].

2. Experimental Procedure

The fabrication procedure is schematically shown in Figures 1(a)–1(h). The procedure consists of two main processes: (i) preparation of the AAO mold with different pore diameter, coating it with a thin SiO2, followed by SAM deposition and (ii) nanoimprinting.

2.1. Preparation of the AAO Mold with Different Pore Diameter

At first, a 1000 nm Al film with a thin Ti underlayer was deposited on a 4 inch (~10.2 cm) circular disc of a Si wafer by thermal evaporation (Figure 1(a)). This disc coated with Al film was cut into pieces and anodized in phosphoric and oxalic acid by a two-step anodization process as described elsewhere [1821]. The first anodization was conducted under 40 V and 160 V in the 2.7 wt% oxalic acid (H2C2O4) and 10 wt% phosphoric acid (H3PO4), respectively, for specific time. Subsequently, the sample was immersed into a mixture solution of H3PO4 ( ) and Cr2O3 ( ) at 70 for specific time to remove the alumina membrane formed during the first anodization, in order to obtain a highly ordered patterned Al surface. Then the second anodization was carried out with the condition the same as the first step. The anodization carried out in oxalic and phosphoric acid provided the small and large interpore distance, respectively. Then the pore widening treatment was conducted in 5 wt% phosphoric acid at 30°C. The pore diameter of anodized alumina fabricated in phosphoric acid and oxalic acid after pore widening treatment is  nm and  nm, respectively.

2.2. Nanoimprinting

The AAO molds were coated with a very thin ~2-3 nm SiO2 layer by atomic layer deposition (ALD) technique followed by the coating with a commonly used silane-based SAM (Heptadecafluoro-1,1,2,2-tetra-hydrodecyl trichlorosilane) (Figure 1(b)). The surface modification of the AAO by SiO2 was the key to the success of the direct use of AAO mold for NIL. The L10-ordered FePt (4 nm) continuous film with film structure of Si/SiO2/CrRu(30 nm)/Pt(3 nm)/FePt(4 nm)/Ru(3 nm) was grown by cosputtering from Pt and Fe targets at 350°C on Si wafer (Figure 1(c)). Then the FePt film was coated with Nanonex-1050 thermal resist by spin coating (Figure 1(d)). Then thermal nanoimprinting was performed by using Nanonex BX200 nanoimprinter on Si wafer and FePt thin film spin coated with thermal resist (Figure 1(e)). The resist flown into the AAO pores remained as pillars after demolding (Figure 1(f)). The FePt film was patterned by RIE and Ar ion milling using the resist pillars as an etching mask (Figure 1(g)). The remaining resist pillars were removed by chemical etching in acetone and RIE that leaves FePt pillars on the substrate (Figure 1(h)). The surface morphology of the mold and imprinted pattern structure was observed with a field-emission scanning electron microscope (FE-SEM). The magnetic properties of the FePt film before and after patterning were measured by a vibrating sample magnetometer (VSM) and a superconducting quantum interference device (SQUID), respectively. The crystallographic property of the continuous FePt film was analyzed by an X-ray diffractometer (XRD).

3. Results and Discussion

We have started with a mold with large pore diameter. Figure 2(a) shows SEM plane view image of the AAO mold fabricated in phosphoric acid. The inset shows the distribution of the AAO pore diameter. The diameter of the AAO pore is  nm. The depth of the pore is about 400 nm estimated from an SEM cross-sectional image. Improvement of the ordering and size distribution of the AAO pores is beyond the scope of this work that can be achieved by optimizing the anodization parameters [20, 21]. Figure 2(b) shows the SEM image of the imprinted resist on an Si wafer by using the mold shown in Figure 2(a) coated with the SAM layer only without any SiO2 coating. The imprinting is carried out at 350 psi, 175°C, for 3 minutes. The resist over more than 50% area is peeled off with the mold as represented by the bright areas. Although resist remains adhered on the rest part of the substrate, no features are observed as indicated by the high-magnification image of the corresponding area shown in the inset. The friction and sticking problem between the mold and the resist is one of the main challenges in nanoimprinting technology. With the nanostructure size becoming smaller and smaller, the surface-to-volume ratio increases dramatically and the friction and sticking problem becomes more severe. When the mold makes contact with the substrate coated with resist, the high surface energy produces a large amount of surface force. With the interaction between surfaces, the profiles of the two surfaces change and reestablish a new energy equilibrium state that produces sticking. Due to the sticking forces between surfaces, the nanosystem produces a large friction force, especially during the demolding process. Among the several options [22, 23] application of the silane-based hydrophobic self-assembled monolayer (SAM), namely, “Heptadecafluoro-1,1,2,2-tetrahydrodecyl Trichlorosilane,” has been reported as the most successful lubrication method [23]. We do not get any imprinting by using this silane-based SAM directly on our AAO mold as shown in Figure 2(b) due to the inferior bonding between Al2O3 and the SAM layer. Then we modify the surface of the AAO mold by coating it with a very thin ~2-3 nm SiO2 by ALD followed by the deposition of the SAM layer on it. Eventually, we achieve excellent imprinting over more than 1 cm2 area with very good replication of the mold as shown in Figure 2(c). The imprinting from even the smallest features is also clearly shown in the inset of Figure 2(c). The diameter of the imprinted features is  nm as shown in the left inset of Figure 2(c). The diameter of imprinted resist pillars is slightly larger than the mold diameter may be due to the swelling of the resist by electron beam during SEM imaging. The coating of the AAO mold with SiO2 layer reduces the surface energy of the mold and enhances the bonding with SAM layer, which is the key of getting successful imprinting.

After achieving successful imprinting of resist pillars with large feature size on a Si wafer, we concentrate our efforts on reducing the feature size and fabricate L10 FePt patterned structure. We grow L10-ordered FePt (4 nm) continuous film with film structure of Si/SiO2/CrRu(30 nm)/Pt(3 nm)/FePt(4 nm)/Ru(3 nm). The FePt layer is cosputtered from Pt and Fe targets at 350°C. This FePt thin film is spin-coated with 150 nm thick thermal resist and patterned by using an AAO mold with  nm pore diameter.

Figure 3(a) shows the plane-view SEM image of the mold. This mold is fabricated by anodizing the Al film in oxalic acid to get smaller pore diameter [21]. The area of the mold is about 1 cm2. The diameter of the pore in the mold is  nm as shown in the inset of Figure 3(a), and the depth of the pore is about 150 nm estimated from an SEM cross-sectional image. The imprinting is performed at 350 psi, 175°C, for 3 minutes. Figure 3(b) shows the SEM cross-sectional image of as imprinted resist pillars on FePt thin film and the inset shows the distribution of resist pillar diameter. The diameter of the imprinted resist pillar is  nm. The height of some of the pillars is smaller than that of the others as indicated by the white arrows. This may be due to the lack of sufficient flatness of the mold and insufficient initial resist thickness. Figure 3(c) shows the plane-view SEM image of the FePt dots on the Si wafer after removing the residual layer and transferring the pattern by Ar ion milling using the resist pillars as an etching mask. The diameter of the FePt dots is  nm. The FePt dot diameter is about 45% smaller than the pore diameter of the mold as well as the as-imprinted resist pillars. This size reduction may occur due to the lateral etching of the resist pillars during residual layer removal by RIE. This size reduction also indicates that the size of the imprinted features can again be tuned by controlling the pore depth and residual layer thickness. Some of the dots as indicated by the black arrows in the inset of Figure 3(c) are almost etched away due to the smaller mask height onto it as indicated by the white arrows in Figure 3(b). As a result, the density of the FePt dots is somewhat smaller than the density of the pores in the mold.

Figures 4(a) and 4(b) show the XRD pattern of the FePt continuous film and M-H loops of the continuous film and patterned structure, respectively. The XRD pattern of the continuous FePt film before patterning exhibits very good L10 FePt (001) texture. The FePt continuous film exhibit very good perpendicular anisotropy with out-of-plane Hc of 3.3 kOe and a squareness ratio of about unity that is good in agreement with the good (001) texture in the XRD diagram. The magnetic property of the patterned FePt structure is measured by using a SQUID at room temperature. The perpendicular coercivity of the patterned structure is about 12 kOe, that is, about 3.5 times larger than that of the continuous film. This Hc value is much lower than that of the isolated FePt islands on MgO [24]. Several mechanisms can be considered for this low Hc value of the patterned structure. First, diffusion may occur at the interface between the Pt layer and the FePt layer as Pt is used as interlayer; therefore, the composition and switching field at the interface may differ from the other part. The FePt at the interface with smaller switching field may be exchange coupled with the adjacent part with larger switching field and reduces the Hc [17, 25]. Second, the redeposition effect may add some disordered FePt onto the outer surface of the pillars. This re-deposited disordered FePt may act as nucleation sites to start the magnetization switching at low field that can reduce the coercivity [26]. In addition, the edge damage of the FePt pillars by ion milling may also be one of the reasons for the low Hc in patterned FePt structure [27].

4. Conclusions

We have shown that the anodized alumina (AAO) fabricated on Si wafer can be used as a large area mold for nanoimprinting. The sticking problem between the mold and the resist has been overcome by modifying the AAO surface by coating it with a very thin SiO2 layer. Moreover, we have successfully fabricated L10 FePt patterned structure with  nm feature size. Optimization of nanoimprinting parameters and flatness of the mold may open the path to fabricate patterned magnetic nanostructures with reduced feature size and high density for practical applications.

Acknowledgments

This work is partially supported by the INSIC’s extremely high areal density recording (EHDR) program and the National Science Foundation (NSF) MRSEC program. A part of the of the work has been carried out in the Nano Fabrication Center (NFC) and Characterization Facilities, the University of Minnesota. The authors are thankful to Dr. Mark Fisher at the NFC, University of Minnesota.