User:RKE2002/sandbox

= Sequential Infiltration Synthesis =

Introduction
Derived from atomic layer deposition (ALD), sequential infiltration synthesis (SIS) is a technique in which a polymer is infused with inorganic material using sequential, self-limiting exposures to gaseous precursors, allowing for the precise control over the composition, structure, and properties of materials. This synthesis involves metal-organic vapor-phase precursors and co-reactants dissolving and diffusing into polymers, interacting with the polymer functional groups via reversible complex formation and/or irreversible chemical reactions yielding desired composite materials, which may be nanostructured. The metal-organic precursor (A) and co-react vapor (B) are supplied in an alternating, ABAB… sequence. Following SIS, the organic phase can be removed thermally or chemically to leave only the inorganic components behind. The precise control over the infiltration and synthesis via SIS allows the creation of materials with tailored properties like composition, mechanics, stoichiometry, porosity, conductivity, refractive index, and chemical functionality on the nanoscale. This empowers SIS to have a wide range of applications from electronics to energy storage to catalysis. SIS is sometimes referred to as “vapor phase infiltration (VPI) ” or “sequential vapor infiltration (SVI) ”.

Despite being a derivation of ALD, the two techniques differ in important ways. SIS involves the 3D distribution of functional groups in polymers whereas ALD is associated with the impermeable 2D distribution of active sites on solid surfaces. In typical ALD processes, the precursor pulses are much shorter as they only need to provide sufficient exposure to saturate the surface chemical groups on the substrate surface. In SIS, the precursor pulse partial pressures and exposure times are typically larger to allow for sufficient precursor to infiltrate a 3D volume through dissolution and diffusion. 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.

History
Sequential Infiltration Synthesis was invented by Argonne National Laboratory scientists Jeffrey Elam and Seth Darling in 2010 and emerged as a distinct concept as a result of trying to apply ALD to polymeric substrates.

SIS involves vapor diffusing into an existing polymer and chemically or physically binding to it. This results in the growth and formation of inorganic structures by selective nucleation throughout the bulk polymer. With SIS, the shapes of various inorganic materials can be tailored by applying them to patterned or nanostructured organic polymers, such as block copolymers.

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. However, the interactions between the ALD precursors and the polymer functional groups were not considered, 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 examined as challenges to address.

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.

Principles and Process
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 photoresist, such as those used in photolithography, microfabrication, and nanolithography. This method involves the sequential deposition of inorganic materials within a patterned resist's micro/nanostructures. By carefully controlling the infiltration of these materials, SIS can precisely engineer the chemical composition and density of the resist, thus enhancing its resistance to common etching processes. This enables technologists to achieve finer feature patterns and greater durability in microfabrication, ultimately advancing the capabilities of semiconductor manufacturing and nanotechnology applications.

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 /lipophilicity, anti-reflection, 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. 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. 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, biosensing, 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, in which it can be used to engineer interfaces and increase light absorption.

Biomedicine
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 macromolecules 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.

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
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 multifunctional 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
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.