Sequential infiltration synthesis

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Derived from

Although SIS is derived from ALD, the two techniques differ in significant ways. SIS involves the 3D distribution of functional groups in polymers, while ALD is associated with the impermeable 2D distribution of reactive sites on solid surfaces. In typical ALD processes, the precursor pulses are much shorter in duration and have lower partial pressure compared to SIS, as they only need to provide sufficient exposure to saturate the surface chemical groups on the substrate surface.[1] In SIS, the precursor pulse partial pressures and exposure times are typically larger compared to ALD to allow for sufficient precursor to infiltrate a 3D volume through dissolution and diffusion.^[1] Unlike the simple precursor saturation on solid substrates in ALD, SIS utilizes the diffusive nature of precursor transport within polymers, which makes the distribution of precursors within the material sensitive to time, pressure, temperature, and polymer chemistry and microstructure.^[1]

History

The diffusion of precursors below the surfaces of polymers during ALD was observed in 2005 by the Steven M. George group when they observed that polymers could uptake trimethyl aluminum (TMA) via absorption within their free volume.^[12] In this study, the interactions between the ALD precursors and the polymer functional groups were not recognized, and the diffusion of precursors into polymer films was considered a problem in some initial studies. Hence, the diffusion and reactions of ALD precursors into polymer films were considered as challenges to address. However, the benefit of these phenomena was demonstrated by Knez and coworkers in their seminal work describing the remarkable increased toughness of spider silk following vapor-phase infiltration.^[9]

Sequential infiltration synthesis was developed by

Since the diffusion of ALD precursors through polymers was observed, SIS was developed to intentionally enable the infusion of inorganic materials such as metal oxides and metals within polymers to yield hybrid materials with enhanced properties. Hybrid materials created via SIS can further be subjected to thermal annealing steps to remove the polymer constituents entirely to derive purely inorganic materials that maintain the structure of the original polymer morphology including mesoporosity.^[16]

Although the early research in SIS focused on a small number of inorganic materials such as Al₂O₃, TiO₂, and ZnO, the technology has matured over the last decade and now includes a wide variety of inorganic materials, polymers, and applications for the resulting hybrid materials as detailed in recent reviews.^{[1][2][3][4][5][6][7]}

Principles and process

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SIS is based on the consecutive introduction of different precursors into a polymer, taking advantage of the material's porosity on the molecular scale. This allows the precursors to diffuse into the material and react with specific functional groups located along the polymer backbone or pendant group. Through the selection and combination of the precursors, a rich variety of materials can be synthesized, each of which can endow unique properties to the material.

The process of SIS involves various key steps, first of which is the materials selection. A suitable substrate material, such as a polymer film, and precursors, typically molecules that can react with the substrate's functional groups, are selected for the infiltration synthesis. The pairing of polymer chemistry and precursor species is vital for acquiring the desired functionalization and modification.

The substrate is placed in a reactor with an inert atmosphere (typically an inert gas or vacuum). The first precursor vapor (e.g., trimethyl aluminum, TMA) is introduced at a sufficiently high vapor pressure and duration such that the precursor molecules diffuse into the substrate. This enables the precursor to "infiltrate" the material and react with the interior functional groups. After a suitable diffusion/reaction time, the reactor is purged with inert gas or evacuated to remove reaction byproducts and unreacted precursor. A second vapor-phase species, often a co-reactant such as H₂O is introduced. Again, the precursor partial pressure and exposure time are selected to allow sufficient time for diffusion into the polymer and reaction with the functional groups left by the first precursor exposure.  The second precursor is then purged or evacuated to complete the SIS cycle. The second precursor also creates new functional groups for reaction with the first precursor for possible subsequent SIS cycles. The infiltration steps can be repeated using the same or different precursor species until the desired modifications are achieved. When the desired infiltrations are achieved, the modified material can undergo further post-treatment steps to enhance the properties and/or stability of the modified layers, such as heating, chemical treatment, or oxidation to remove the organic polymer.

SIS is an especially powerful technique when paired with block copolymers (BCPs). Block copolymers such as polystyrene-block-poly methyl methacrylate, PS-b-PMMA, can spontaneously microphase separate to form a rich variety of periodic mesoscale patterns. If the SIS precursors are selected to react with just one of the BCP components but not with the second component, then the inorganic material will only nucleate and grow in that component. For instance, TMA will react with the PMMA component of PS-b-PMMA but not with the PS component.  Consequently, SIS using TMA and H₂O will form Al₂O₃ only in the PMMA. Subsequent removal of the PS-b-PMMA using an oxygen plasma or by annealing in air will convert the organic mesoscale pattern into an inorganic, Al₂O₃ pattern that is more chemically and thermally robust compared to the original polymer.

The principles and process described is an overview of SIS; it is important to note that there are variations and optimizations to the synthesis process depending on the desired materials and their applications.

Applications

SIS has gained much attention in various fields due to its ability to precisely modify and functionalize polymeric materials.

Lithography

One of the main applications of SIS is in the enhancement of etch resistance in lithographic

Surface coatings

Another major application of SIS is in the field of surface coatings, as it enables the development of advanced functional coatings with tailored properties. With the sequential infiltration of different precursors into the material, SIS allows for the creation of coatings with enhanced properties and performance such as durability, corrosion resistance, oleophilicity^[18][19]/lipophilicity, anti-reflection,^[20] and/or improved adhesion to substrates. Such an application of SIS can be used for protective coatings for metals, anti-fouling coatings for biomedical applications, and coatings for optical and electronic devices.^[21][22][23] In this application, the diffusion and reaction of the SIS precursors below the polymer surface facilitate a bulk-like transformation such that the effective thickness of the surface coating (e.g., several microns) is much larger than the film thickness that would result using the same number of atomic layer deposition (ALD) cycles on a conventional, dense substrate (e.g., a few nanometers).

Sensors and actuators

SIS with its precise control over material properties is a powerful method to develop sensors and actuators.^[24][25] The functional layers that are created through the selective infiltration of specific precursors can enhance sensitivity, selectivity, and response of sensors, which have applications in gas sensing, chemical sensing, bio sensing, and environmental monitoring. SIS is also promising when used to engineer actuators with tunable properties. This enables the fabrication of devices on micro and nano scales for an assortment of applications.

Energy devices

SIS has also shown promise in the field of energy devices, especially in improving the performance and stability of energy storage and conversion systems. Employing SIS and the correct precursors, the technique can modify the surfaces and interfaces of materials used in batteries, supercapacitors, and fuel cells, enhancing charge transport, electrochemical stability, and energy density. SIS is also being explored for its applications in photovoltaics,^[26] in which it can be used to engineer interfaces and increase light absorption.

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SIS is a suitable tool for surface modifications to improve biocompatibility, bioactivity, and controlled drug release, making it suitable for some biomedical applications. Polymers and bioactive macro-molecules that are treated with SIS can obtain coatings with developed cell adhesion and reduced bacterial adhesion as well as providing a medium for the controlled release of therapeutics. Such properties have applicability in biomedicine such as implantable medical devices, tissue engineering, and drug delivery systems.

Mechanical Properties

An early application of SIS was to improve the mechanical properties of protein structures in biomaterials. For instance, when spider dragline silk is infiltrated with Al₂O₃ using trimethyl aluminum (TMA) and H₂O, the toughness is improved by nearly an order of magnitude.^[9]

Advantages and limitations

The advantages and disadvantages of SIS are outlined. It is important to note that the advantages and limitations of SIS are continually being explored, addressed, and improved upon via ongoing research and development efforts in the field.

Advantages

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SIS allows for precise control over the composition, structure, and properties of materials. The sequential nature of the synthesis process enables the integration of multiple materials and the creation of complex and multi-functional nanostructures. SIS enables atomic-level precision in controlling the deposition of precursor materials. This high level of precision allows for the creation of nanostructures with uniform dimensions, well-defined interfaces, and tailored properties.

SIS is a versatile fabrication technique amenable to a diverse range of combinations of polymer chemistries and precursor species. By selecting specific precursor materials, researchers can tune the properties of the fabricated materials, which include but are not limited to electrical conductivity, optical properties, and catalytic activity. This empowers various applications in electronics, photonics, energy devices, separations, and more.

Limitations

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One of the main challenges of SIS is the need to perform the process in an inert environment. Creation of a vacuum and/or introduction of inert gas carries a cost that may be prohibitive for certain applications. A second challenge relates to the complexity of the diffusion-reaction process, where the specifics of the reactor configuration and process parameters can have substantial impact on the final material. This can pose limitations in terms of process optimization, reproduction, and scalability. Even though SIS can be applied to a wide range of materials, there are also materials that may not be suitable for the SIS process. The relatively slow diffusion of SIS precursor vapors through polymers can make SIS over macroscopic distances time-consuming. For instance, the infiltration of millimeter distances into a polymer may require precursor exposure times of several hours. For comparison, ALD of thin films on dense surfaces that do not involve diffusion into the substrate would require exposure times of <1 s using the same precursors.

References