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Multiphoton lithography

Multiphoton lithography is a high-resolution additive that employs nonlinear optical processes, such as , to fabricate complex three-dimensional microstructures and nanostructures from photosensitive materials. By focusing ultrafast pulsed lasers, typically near-infrared lasers, into a photopolymerizable , the method confines chemical reactions like to a tiny focal volume, where the probability of multiphoton is highest due to the quadratic intensity dependence, enabling sub-diffraction-limited feature sizes as small as 100 without the need for or scanning in multiple dimensions. This direct laser writing approach allows for true freedom in design, distinguishing it from traditional planar . The foundational principle of multiphoton lithography relies on the simultaneous absorption of two or more photons by a molecule, exciting it to a state that triggers crosslinking in monomers or oligomers, forming solid structures by as the beam is scanned. Pioneered in 1997 by Shoji Maruo, Osamu Nakamura, and Satoshi Kawata, the technique was first demonstrated using a titanium-sapphire at 790 nm with 200 fs pulses to polymerize urethane acrylate resins, producing microstructures like micro-cantilevers and bridges with resolutions below the limit. Subsequent advancements, including refinements in efficiency and strategies, have pushed resolutions to below 10 nm in some cases, with key contributions from researchers like Saulius Juodkazis and Mangirdas Malinauskas in material optimization and parallel processing. Key advantages of multiphoton lithography include its ability to process a wide range of materials, such as acrylates (e.g., IP-Dip, SU-8), hybrid organic-inorganic resins (e.g., Ormocer), hydrogels for , and even ceramics via post-processing, while supporting multifunctional doping with nanoparticles or dyes for enhanced properties like or . Unlike conventional methods, it offers unparalleled precision for arbitrary geometries, including overhangs and internal voids, and has evolved to include capabilities through stimuli-responsive materials. Challenges persist in throughput, addressed by innovations like multi-focal scanning and continuous projection systems, making it suitable for prototyping rather than . Applications span , where it fabricates waveguides, microlenses, and metamaterials; , enabling tissue scaffolds, microneedles for , and organ-on-chip devices; and microelectromechanical systems () for sensors and actuators. In , it has produced high-numerical-aperture lenses and diffractive elements directly on tips. Biomedical uses leverage biocompatible resins to create patient-specific implants and vascular networks mimicking extracellular matrices. Overall, multiphoton lithography's versatility positions it as a cornerstone for nanoscale in interdisciplinary fields.

Principles

Multiphoton Absorption

Multiphoton absorption is a nonlinear in which a simultaneously absorbs two or more photons, each with lower than the , to reach a higher electronic state whose equals the sum of the absorbed photons' energies; this process proceeds through virtual intermediate states that exist only transiently during the absorption. The concept was theoretically predicted in 1931 by Maria Göppert-Mayer, who described the quantum mechanical basis for such third-order processes in atoms and . Experimental observation followed in 1961 with the first demonstration of two-photon in doped with ions using a . In the context of multiphoton lithography, two-photon absorption is the predominant mechanism due to its balance of efficiency and practicality, involving the near-simultaneous uptake of two photons to bridge the energy gap typically matched by a single ultraviolet or visible photon. Higher-order processes, such as three-photon absorption, require the simultaneous absorption of three photons and exhibit a cubic intensity dependence (I³), but they demand significantly higher light intensities and occur with much lower probability, making them rarer in standard lithographic applications. The physics underlying two-photon absorption dictates that the absorption probability is proportional to the square of the light intensity (I² dependence), which confines the excitation to the intense focal volume of a tightly focused laser beam, enabling sub-wavelength precision. The efficiency of two-photon absorption is characterized by the two-photon cross-section δ, typically measured in Göppert-Mayer (GM) units, where 1 GM = 10^{-50} cm⁴ s photon^{-1}, reflecting the molecular propensity for the process. The rate of population of the follows a quadratic intensity dependence, expressed as the excitation rate ∝ σ I² / (hν)², where σ denotes the two-photon cross-section, I is the light intensity, h is Planck's constant, and ν is the frequency; this formulation arises from applied to the nonlinear optical response. To achieve the peak intensities (often >10^{12} W/cm²) required for appreciable rates without excessive average power, femtosecond pulsed lasers operating in the near-infrared spectrum (700–1000 nm) are employed, delivering ultrashort pulses (∼100 fs) at high repetition rates (∼80 MHz) while limiting thermal effects through low duty cycles. Compared to linear single-photon absorption, which excites molecules uniformly along the entire propagation path and suffers from strong and at shorter wavelengths (e.g., UV), multiphoton localizes delivery to the due to its nonlinear threshold, surpassing the optical (∼λ/2). Furthermore, the longer near-IR wavelengths used in multiphoton processes penetrate deeper into optically thick materials, experiencing minimal linear and reduced (∝ 1/λ⁴), which is particularly advantageous for volumetric fabrication in media.

Polymerization Mechanism

In multiphoton lithography, the polymerization mechanism relies on photopolymerization processes—primarily radical or cationic types—triggered by photoinitiators excited via multiphoton absorption in the focal volume of a femtosecond laser beam. Radical polymerization involves the generation of free radicals from photoinitiators, such as those undergoing homolytic cleavage upon excitation, while cationic polymerization employs photoacid generators that release protons to initiate ring-opening reactions in epoxide-based systems. These mechanisms convert the localized energy from multiphoton absorption into chemical bonds, forming solid polymer networks from liquid monomers or oligomers without significant heat accumulation due to the ultrafast pulse durations. The step-by-step process commences with photoexcitation of the to an excited electronic state, typically a or triplet, followed by the rapid formation of reactive species: via bond dissociation in Type I initiators or hydrogen abstraction in Type II systems, or cations and protons in cationic variants. occurs as these species add to double bonds in monomers for or coordinate with oxygen for cations, creating active chain ends. proceeds through sequential addition of monomers to the growing chain, accelerating as the radical or cationic concentration builds locally. Termination finally halts the reaction via radical recombination, , or cationic by counterions or nucleophiles, ensuring controlled chain lengths. A defining feature is the threshold behavior, where initiates solely above a critical —typically on the order of GW/cm²—beyond which the generation rate of reactive outpaces their and recombination, confining the to the sub-micron focal . This nonlinearity enables voxel-by-voxel solidification, with the effective (~0.1–1 μm³) governed by the optical point-spread function, yielding sub-100 nm lateral resolutions. In crosslinking formulations, the process reaches a gel point when sufficient interconnections form an insoluble network, often accompanied by volumetric shrinkage (up to 10–15% in acrylates), which can induce but is addressed through post-curing via or additional exposure to complete unreacted sites and bolster mechanical integrity. Laser parameters critically modulate initiation efficiency and threshold: pulses (e.g., 50–150 fs) deliver high peak intensities with minimal diffusion, preventing unwanted heating; repetition rates (typically 70–100 MHz) influence cumulative dose and heat buildup, optimizing for high-throughput without resolution loss; and wavelengths in the near-infrared (700–800 nm) enhance tissue-like penetration while matching cross-sections of common initiators, thereby tailoring the reactive species yield.

History

Invention and Early Demonstrations

Multiphoton lithography emerged in the late 1990s as an extension of earlier advancements in multiphoton microscopy, pioneered by Winfried Denk and colleagues in 1990, which demonstrated nonlinear optical excitation for high-resolution imaging deep within biological samples, and single-photon stereolithography, invented by Charles Hull in 1986, which enabled layer-by-layer 3D printing using ultraviolet light to cure photopolymers. These foundations inspired the adaptation of nonlinear absorption principles to achieve precise, volumetric control in microfabrication without the need for physical masks or sequential layering. The first experimental demonstration of multiphoton lithography occurred in 1997 at Osaka University, where Shoji Maruo, Osamu Nakamura, and Satoshi Kawata created three-dimensional microstructures in a photopolymer resin composed of urethane acrylate monomers and oligomers mixed with photoinitiators. Using a Ti:sapphire femtosecond laser operating at 790 nm with 200 fs pulses, the team induced two-photon absorption to polymerize resin selectively at the laser focus, producing complex 3D structures such as spirals and bridges with feature sizes around 1-2 μm. This maskless approach addressed key challenges in achieving true volumetric fabrication by employing galvanometer scanners to steer the focused beam in three dimensions, enabling arbitrary geometries unattainable with conventional lithography. Building on this breakthrough, the Kawata group published seminal work in 1999 demonstrating the fabrication of three-dimensional structures, including woodpile-like lattices, through two-photon photopolymerization of , showcasing potential for optical applications with resolutions limited to 1-2 μm by optical and material properties. Parallel efforts around 1999 by Martin Gu explored multiphoton processes for biological imaging and potential micromachining applications, highlighting the technique's versatility for life sciences. By the early , these proofs-of-concept shifted focus toward commercial viability, with initial resolutions constrained by and formulations.

Key Technological Milestones

In the early , multiphoton lithography saw significant improvements in resolution and fabrication techniques, building on foundational demonstrations to enable more complex nanostructures. Between and , researchers advanced sub-diffraction-limited features, with key works achieving resolutions around 100-120 nm through optimized processes in acrylic resins, allowing for the creation of functional microdevices with finer details. For instance, in 2004, woodpile photonic structures were fabricated, demonstrating enhanced and paving the way for periodic nanostructures. By , the introduction of nanostereolithography with sub-regional slicing methods increased throughput for high-aspect-ratio features, marking a shift toward practical . A pivotal commercialization milestone occurred in 2007 with the founding of Nanoscribe GmbH, which released its first high-performance laser lithography system based on two-photon polymerization, making the technology accessible beyond academic labs through user-friendly setups like the Photonic Professional series. This enabled reliable sub-micrometer for and , transitioning multiphoton lithography from experimental prototypes to industrial tools. By the mid-2010s, this shift had broadened adoption in manufacturing, with systems supporting resolutions down to 65 nm as demonstrated in optimized resins. During the , innovations in beam manipulation dramatically boosted processing speed and parallelism. Multi-focal and holographic beam shaping techniques, using spatial light modulators to generate multiple foci, allowed simultaneous at various sites, increasing throughput by orders of magnitude for large-area patterning. A representative example from 2014 involved real-time hologram calculation for 3D multi-focus , enabling complex microstructures with sub-200 nm features in parallel. These methods addressed serial writing limitations, facilitating applications in scalable micro-optics. Additionally, the 2012 for , particularly STED by , inspired integrations that enhanced lithography resolution. Roots in early proposals evolved into practical STED-inspired variants by the early , achieving sub-100 nm resolutions—such as 55 nm structures and 120 nm spacing—through photoinhibition of outside the focal spot. In the 2020s, multiphoton lithography has incorporated dynamic and intelligent elements, with resolutions pushing toward 10-20 nm in advanced setups. Developments in leverage stimuli-responsive materials, such as shape-memory polymers, to create time-evolving structures post-fabrication, with examples including light-driven actuators resolved at hundreds of nanometers. Integration of for design optimization has further refined processes, using to predict and adjust parameters like power and scan paths for defect-free nanoscale prints. Reviews in 2023 highlighted two decades of progress, emphasizing techniques that combine multiphoton methods with computational tools for unprecedented precision and versatility.

Materials

Organic Photoresists

Organic photoresists are widely used in multiphoton due to their compatibility with or mechanisms triggered by multiphoton absorption. These materials typically consist of monomers or oligomers mixed with photoinitiators, offering tunable properties for high-resolution fabrication. Acrylate-based photoresists, such as IP-Dip from Nanoscribe, dominate applications requiring sub-micrometer resolution for complex structures, owing to their kinetics that enable rapid curing. These resists feature low (around 5-50 mPa·s) for easy handling and dip-in processes, high photosensitivity with initiators like Irgacure 369 (2-hydroxy-2-methylpropiophenone-based), and good suitable for biomedical scaffolds. However, they exhibit volumetric shrinkage of 5-15% during , which can induce in intricate designs. Formulations often include multifunctional acrylates as monomers/oligomers, such as ethoxylated diacrylate or pentaerythritol triacrylate, along with crosslinkers like dipentaerythritol hexaacrylate and inhibitors (e.g., ) to control premature gelation and threshold exposure. Epoxy-based photoresists, exemplified by SU-8, are favored for negative-tone patterning in and high-aspect-ratio structures due to their superior and minimal shrinkage (typically <5% volumetric). These materials provide low viscosity formulations (50-200 mPa·s) for spin-coating or direct writing, enhanced photosensitivity via integrated cationic initiators, and adequate biocompatibility for microfluidic devices. SU-8 consists of epoxy novolac resins derived from bisphenol A diglycidyl ether, diluted in solvents like cyclopentanone, with optional additives for viscosity control. Crosslinking occurs through ring-opening polymerization, yielding robust thermosets with Young's moduli up to 5 GPa. Processing of these organic photoresists involves pre-exposure application via spin-coating or dispensing, followed by femtosecond laser exposure for selective polymerization, and post-exposure development to remove unexposed regions. Common developers include propylene glycol monomethyl ether acetate (PGMEA) for SU-8 to achieve clean removal without swelling, while acrylate resists like IP-Dip are typically rinsed in isopropyl alcohol or ethanol mixtures for gentle dissolution. A final hard bake may stabilize the structures, minimizing residual solvent effects.

Inorganic and Hybrid Materials

In multiphoton lithography, inorganic materials such as sol-gel derived glasses and ceramics provide enhanced mechanical and optical properties compared to purely organic resists, enabling the fabrication of durable microstructures for harsh environments. Sol-gel processes typically involve the hydrolysis and condensation of metal alkoxides to form inorganic networks within photosensitive matrices, allowing precise three-dimensional patterning via two-photon absorption. For instance, silica-acrylate composites doped with transition metal oxide nanoparticles, like zirconium or titanium, have been used to create photonic crystals with submicron periodicity through holographic lithography, offering improved structural integrity and optical performance. Hybrid materials, combining organic and inorganic components, further optimize performance by mitigating issues like brittleness in pure inorganics. Ormosils (organically modified silicates), such as zirconium-silicon-based formulations like SZ2080, incorporate silica nanoparticles into hybrid resins for high optical quality in micro-lenses and scaffolds, with applications in tissue engineering and medical implants. Similarly, Ormocers (organic-modified ceramics) blend acrylates with siloxanes derived from precursors like tetraethoxysilane (TEOS), achieving low volumetric shrinkage below 2% during polymerization and high refractive indices exceeding 1.5, which are ideal for photonic woodpile structures with 100 nm resolution. Synthesis of these hybrids often entails incorporating inorganic precursors into organic matrices, followed by multiphoton-induced hydrolysis and condensation to form a crosslinked network, as demonstrated in two-photon controlled sol-gel processes using photoacids or photobases. These materials exhibit superior thermal and chemical stability, making them suitable for photonics and micromechanics, though hybrids address inherent brittleness through flexible organic phases. In the 2010s, advancements in zirconia ceramics via two-photon polymerization enabled the additive manufacturing of alumina-toughened zirconia (ATZ) structures with nanoscale resolution (<1 μm), with the photocurable slurry achieving high transparency (65% at a penetration depth of 0.1 mm) to enable effective polymerization, followed by debinding and sintering to yield dense ceramic structures suitable for bone implants and piezoelectric devices. Metal-organic frameworks (MOFs) represent another inorganic class, where two-photon polymerization directly fabricates intricate nanostructures within single MOF crystals, leveraging their porous architecture for sensing and photonic applications without additional resists.

Fabrication Techniques

Two-Photon Polymerization

Two-photon polymerization (2PP) utilizes two-photon absorption to confine the polymerization reaction to the focal volume of a femtosecond laser beam, enabling the direct writing of three-dimensional microstructures with sub-micrometer precision. This baseline method in multiphoton lithography relies on the nonlinear excitation of photoinitiators, which occurs only at intensities exceeding a threshold within the diffraction-limited focal spot. The standard experimental setup features a mode-locked Ti:sapphire femtosecond laser, typically tuned to 780 nm with a pulse duration of 100-140 fs and a repetition rate of 80 MHz, to deliver high peak intensities while minimizing thermal effects. The laser beam is expanded, attenuated if needed, and focused through a high numerical aperture (NA > 1.3) oil-immersion objective lens, achieving a focal spot size approximated by \lambda/(2\text{NA}), where \lambda is the wavelength. For precise voxel addressing, scanning systems combine galvanometer mirrors for rapid xy-plane movement and piezoelectric or linear motor-driven stages for z-axis control, with closed-loop feedback ensuring nanometer-scale positioning accuracy. Fabrication begins with applying a photosensitive to a via drop-casting or immersion in a sample chamber. The focused is then scanned through the either layer-by-layer or in a continuous volumetric path, inducing where the local intensity surpasses the initiation threshold, forming solid voxels or lines. Post-exposure, the structure is developed in a to dissolve uncured material, yielding the freestanding object; for compositions, optional can enhance properties. is governed by the focal spot dimensions and polymerization threshold, yielding lateral features of 100-200 nm and axial elongation up to 500 nm, as demonstrated in early work fabricating 120 nm lines. Dedicated software converts 3D CAD models into executable scan paths, often via intermediate STL triangulation followed by slicing into layers and generation of GWL or similar control codes, while algorithms compensate for resin shrinkage (typically 5-20%) and spherical aberrations from refractive index mismatches. This maskless, alignment-free approach uniquely enables the creation of intricate geometries, such as overhanging cantilevers or suspended bridges, without sacrificial supports or multi-step assembly.

Advanced Variants

Advanced variants of multiphoton lithography have emerged to overcome limitations in resolution and fabrication speed inherent to standard two-photon polymerization, enabling sub-50 nm features and for complex structures. These techniques build on the core nonlinear absorption principle but incorporate optical depletion, multi-beam shaping, or higher-order photon processes to enhance performance in demanding applications. STED-inspired lithography employs a depletion beam to inhibit polymerization outside the excitation focus, effectively shrinking the point spread function and achieving resolutions below the limit. Developed in the 2010s, this approach draws from stimulated emission depletion microscopy pioneered by Stefan Hell's group, adapting it for photoinhibitory resists where a secondary deactivates initiators in the doughnut-shaped periphery of the focal volume. Early demonstrations reported structure sizes as small as 55 nm and resolutions of 120 nm using two-photon excitation combined with . Subsequent refinements, including cationic systems for resists, have pushed lateral resolutions to around 50 nm while maintaining compatibility with biocompatible materials. These methods address serial writing's resolution constraints by confining the reactive volume, though they require precise beam alignment and specialized photoresists. To tackle throughput limitations of point-by-point scanning, multi-focal and holographic techniques utilize spatial light modulators (SLMs) to generate multiple or shaped foci for parallel writing. Holographic beam shaping divides the laser into dozens to thousands of independently addressable foci, accelerating fabrication by factors of 10 to 100 compared to single-beam methods, with reported speeds enabling complex 3D structures in minutes rather than hours. For instance, SLMs integrated with galvanometric scanning have demonstrated high-throughput printing of micro-optical elements with sub-100 nm resolution across large areas. Digital holography variants further allow ultrafast nanofabrication of up to 2000 programmable foci, supporting dynamic pattern adjustments for photonic or mechanical prototypes. These parallel approaches mitigate serial bottlenecks but demand computational optimization for hologram generation and can introduce aberrations in thick samples. Three-photon polymerization extends multiphoton lithography to longer wavelengths, facilitating deeper penetration in scattering media such as biological tissues or turbid resins. By using near-infrared pulses around 1.5–2 μm, this variant achieves axial depths of hundreds of micrometers while maintaining sub-micrometer lateral through the cubic dependence on . Seminal work in the mid-2000s demonstrated 3D structures with 500 nm features, and recent tunable-laser implementations have refined it for x-photon processes, enabling fabrication in optically challenging environments like bioprinting. This addresses penetration limits in standard techniques but requires higher pulse energies to compensate for the lower absorption cross-section. Notable 2020s advancements include in-situ curing within microfluidic channels, where multiphoton lithography fabricates constraints or scaffolds directly around living cells for dynamic biological studies. This integration allows real-time structuring of hydrogels or in flow systems, producing biocompatible devices with 100–200 nm features without post-processing removal. Record resolutions have reached 9 nm laterally through optimized beam lithography in resists, setting benchmarks for nanoscale precision. These developments collectively enhance scalability, with ongoing efforts focusing on setups combining variants for balanced and speed, including emerging four-photon processes for further reduced intensities as of 2025.

Applications

Biomedical Engineering

Multiphoton lithography has emerged as a key technique in , particularly for fabricating complex, biocompatible structures that interface with biological systems in . This method enables the precise creation of three-dimensional (3D) architectures at the micro- and nanoscale, supporting applications in , implantable devices, and . By leveraging two-photon polymerization, it allows for the use of hydrogels and other soft materials that mimic the , promoting cell viability and integration without eliciting adverse immune responses. In , multiphoton lithography is widely used to produce 3D porous scaffolds that replicate the , featuring controlled ranging from 10 to 500 μm to facilitate nutrient and cell infiltration. These scaffolds, often fabricated from biocompatible materials such as diacrylate (PEGDA), support robust cell growth and tissue regeneration; for instance, riboflavin-initiated PEGDA scaffolds have demonstrated high structural fidelity and cytocompatibility for and repair. Acrylates like PEGDA are favored for their FDA-approved status and tunable properties, enabling seamless with tissues. Additionally, the technique's resolution permits nanoscale surface texturing on scaffolds, enhancing through topographic cues that promote formation and cytoskeletal alignment. For , multiphoton lithography fabricates microneedle arrays with tip diameters under 100 μm, designed for painless penetration and sustained release in hydrogels. These structures, such as those made from photocurable polymers, enable efficient delivery of macromolecules like proteins or nucleic acids by creating hollow or dissolving features that minimize . In implants, the technology supports custom vascular networks and organ-on-chip models, including perfused channels mimicking blood vessels for improved oxygenation in engineered s; examples include vascular grafts with lumen diameters as small as 50 μm, tested for endothelial cell lining. Corneal implants developed in the , such as limbal scaffolds for epithelial regeneration, highlight its role in ocular restoration. The high of these constructs allows for implantation and testing, with minimal observed in animal models over extended periods. Recent developments in the have shifted toward bioresists in multiphoton lithography, incorporating stimuli-responsive materials that adapt to environmental cues like or for dynamic tissue interfaces. These smart hydrogels, such as those swelling in response to changes for controlled elution or contracting at to guide , expand applications in adaptive implants and responsive scaffolds. This evolution enhances the functionality of biomedical devices, enabling real-time modulation in regenerative environments. As of 2025, research continues to address technical challenges in using two-photon polymerization for , focusing on scaling from cells to functional organ models.

Microfluidics and Micromechanics

Multiphoton lithography, particularly through two-photon polymerization (TPP), enables the fabrication of complex three-dimensional microfluidic channels with sub-micrometer features, facilitating precise control over fluid dynamics such as mixing and separation. These channels, often with resolutions down to sub-100 nm in height, can be integrated into hybrid structures combining TPP-printed polymer elements with glass substrates to maintain optical transparency essential for in situ monitoring. Unlike traditional two-dimensional lithography, TPP allows the creation of buried or embedded channels that traverse multiple layers without surface access, enabling designs impossible with planar techniques and achieving tolerances below 1 μm for accurate flow control in lab-on-a-chip devices. For instance, in the early 2000s, researchers demonstrated droplet generators using TPP to produce monodisperse emulsions with channel features around 1-5 μm, advancing applications in chemical synthesis and analysis. To enhance functionality, these microfluidic structures are frequently hybridized with (PDMS) for sealing, where TPP-printed masters serve as molds for PDMS casting, combining the high-resolution features of TPP with the and flexibility of PDMS. This integration supports scalable production of devices for precise fluid manipulation, such as serpentine mixers or separation channels, where sub-μm dimensions minimize lengths and improve efficiency. High-resolution TPP techniques ensure feature fidelity in these hybrids, allowing seamless interfaces between and layers. In micromechanics, TPP facilitates the direct fabrication of movable components like , cantilevers, and hinges from epoxy-based resins such as IP-Dip or hybrid ceramic-polymer materials, eliminating the need for post-assembly in micro-electro-mechanical systems (). Early demonstrations in the 2000s produced freely rotating microgears with integrated shafts, approximately 10-50 μm in diameter, showcasing the ability to create articulated structures in a single exposure without supports. Cantilevers and hinges, often with lengths of 50-200 μm and thicknesses under 1 μm, exhibit mechanical properties suitable for sensing or actuation, with Young's moduli tunable via material selection to match or elastomers. These components enable compact devices with high precision, as TPP's resolution supports tolerances below 500 nm for reliable motion. By the 2010s, TPP extended to actuators, where or hybrid materials formed compliant hinges and cantilevers for deformation under stimuli like heat or , achieving strokes up to several hundred micrometers in microstructures smaller than 100 μm. This capability supports untethered microactuators for tasks requiring flexibility, such as crawling or gripping at the microscale, with the process allowing of moving parts directly within assemblies. In 2025, two-photon has been exploited to create magnetic nanostructures with complex geometries, enabling new functionalities in microactuators and sensors.

Photonics and Optics

Multiphoton lithography enables the precise fabrication of photonic crystals, which are periodic structures designed to manipulate propagation through photonic bandgaps. In particular, three-dimensional woodpile structures, consisting of stacked layers of orthogonally oriented rods, have been realized using two-photon with lasers, achieving constants around 1.2–1.4 μm. These structures exhibit photonic bandgaps in the near- region, with gap-to-midgap ratios of approximately 11% centered at wavelengths such as 1637 nm, demonstrating suppression rates of about 50% in the stacking direction within a 5° angular confinement. Such bandgaps in the and visible ranges facilitate applications in confinement and waveguiding by prohibiting certain wavelengths from propagating. The technique also supports the creation of micro-optical elements, including lenses, gratings, and metasurfaces, leveraging its ability to produce sub-wavelength features with high fidelity. Aspherical and Fresnel microlenses, for instance, have been printed with profile errors below 0.2%, while Dammann gratings and blazed gratings achieve high diffraction efficiencies exceeding 80% across the . Metasurfaces, such as polarization rotators and spiral phase plates for generating vortex beams, benefit from the method's capacity to form twisted or freeform geometries on substrates like optical fibers. organic-inorganic materials, such as ORMOCER® and SZ2080™, provide refractive indices up to 1.62, enabling high index contrast for enhanced light manipulation without significant shrinkage during processing. Inorganic hybrids further contribute to tunable refractive properties in these components. Notable examples include integrated waveguides fabricated in the 2010s using Ormosil-based resists like OrmoComp®, where two-photon lithography produced optically isolated structures with predefined profiles for efficient light transport. In the 2020s, diffractive optics such as multilevel metalenses with numerical apertures up to 0.96 have been developed for and displays, focusing light to spots as small as 0.84 μm with efficiencies around 32%. The alignment-free nature of multiphoton lithography allows for the direct writing of complex, interconnected geometries without sequential masking, facilitating intricate designs like multimode interferometers. Additionally, its resolution below the diffraction limit enables sub-wavelength features essential for metamaterials that exhibit exotic optical responses, such as . As of 2025, advances in and multi-photon printing have enabled the creation of dynamic photonic devices that respond to external stimuli, further expanding applications in nano-photonics. Performance in these photonic devices is enhanced by the smooth surfaces achieved through precise , resulting in low propagation losses, such as 0.03 / in ultra-compact waveguides over the 650–700 range. This smoothness minimizes , supporting operation in visible and wavelengths for integrated optical circuits.

Advantages and Limitations

Key Benefits

Multiphoton lithography offers sub-diffraction limited , routinely achieving lateral features below 100 and axial resolutions around 300 , which exceeds the approximately 200 minimum feature size of traditional UV due to the quadratic dependence of on light intensity that localizes the to the . This high precision enables voxel-by-voxel control for fabricating arbitrary complex geometries with minimal heat-affected zones, as the nonlinear process confines energy deposition to sub-micrometer volumes, avoiding thermal damage to surrounding material. A primary advantage is its true volumetric 3D fabrication capability, allowing single-step creation of intricate three-dimensional structures without the layering artifacts and associated with or other additive manufacturing techniques that rely on sequential layer deposition. Furthermore, the use of near-infrared lasers facilitates deeper penetration depths of hundreds of micrometers into materials, including media like biological tissues or hydrogels, compared to the surface-limited depths of single-photon UV processes that suffer from rapid attenuation. The technique's versatility stems from its maskless nature, which eliminates the need for costly photomasks and enables with a wide range of materials, including polymers, hybrids, and inorganics, thereby reducing fabrication costs for custom designs. Notably, it supports the creation of nanoscale features directly in biocompatible materials such as PEGDA hydrogels or GelMA, paving the way for by enabling patient-specific microstructures like tissue scaffolds or devices with sub-micrometer precision.

Challenges and Developments

One of the primary limitations of multiphoton lithography is its slow serial writing process, which typically requires hours to fabricate structures on the centimeter scale due to low scanning speeds typically ranging from 0.1 to 10 mm/s. This point-by-point approach severely restricts throughput, confining practical fabrication to small volumes typically under 1 mm³. Additionally, material shrinkage during and post-processing can reach up to 15%, leading to distortions in the final structures and complicating precise replication of designs. High equipment costs, often exceeding 100,000 USD for commercial direct writing systems, further hinder widespread adoption. Throughput is also impeded by photoinitiator bleaching, which consumes the initiator during exposure and reduces polymerization efficiency at greater depths, limiting the viable working volume and uniformity in thicker samples. Scalability for mass production remains a significant challenge, as the serial nature and low throughput make it impractical for large-area uniformity or high-volume manufacturing, often resulting in inconsistencies over extended areas. These issues collectively position multiphoton lithography as a research tool rather than a routine industrial process. Recent developments have focused on parallelization techniques, such as holographic beam shaping, which enable simultaneous exposure at multiple foci and achieve up to 100-fold speedups in fabrication rates. New low-shrinkage resists, including hybrid organic-inorganic formulations, have been engineered to minimize volumetric contraction to below 5%, improving structural fidelity. Hybrid approaches combining multiphoton lithography with extrusion-based printing offer enhanced scalability by integrating high-resolution features with faster bulk deposition. Looking ahead, integration of for process optimization, including predictive modeling of exposure parameters and shrinkage compensation, promises further efficiency gains. As of 2025, research emphasizes making multiphoton lithography more viable for industrial applications, with market projections indicating significant expansion through 2032. Notably, between 2023 and 2025, innovations in multiphoton lithography have enabled the creation of structures with dynamic responsiveness, such as pH-sensitive microresonators that swell or shrink reversibly, addressing previous limitations in static designs.