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Reactive-ion etching

Reactive-ion etching (RIE) is a technique in that utilizes a low-pressure to remove material from a through a combination of chemical reactions and physical bombardment, enabling highly anisotropic for precise pattern transfer. In the RIE process, a reactive gas such as CF₄ or SF₆ is introduced into a at pressures between 10⁻¹ and 10⁻³ , where radiofrequency (RF) power applied to electrodes generates containing reactive radicals and . These diffuse to the surface, where chemical reactions form volatile by-products, while positively charged are accelerated by an toward the negatively biased , enhancing etch directionality through and surface activation. The by-products are then desorbed and evacuated, completing the etch cycle. This method differs from isotropic wet etching, which relies solely on chemical and often causes undercutting of masked , by providing directional control that supports sizes below 100 and high ratios. Compared to pure , RIE incorporates ion energy for greater and selectivity, though it requires careful parameter tuning to balance etch rate, uniformity, and mask durability. Key advantages include reduced chemical , compatibility with , and minimal substrate , making it superior for high-volume . RIE is essential in applications such as fabrication, where it etches silicon, oxides, and metals; and NEMS devices for creating sensors and actuators; and for high-aspect-ratio structures in materials like SiC and GaN. Advanced variants, such as (DRIE), extend its capabilities for deeper trenches via cyclic processes like the method.

History

Invention and Early Development

The origins of reactive-ion etching trace back to the late 1960s, when Stephen M. Irving developed as a dry alternative to traditional wet chemical methods for processing. Working at Signetics Corporation, Irving demonstrated the use of oxygen to strip layers from wafers, recognizing its potential for etching other materials like and aluminum through reactive gases such as fluorine- or chlorine-based compounds. This innovation, detailed in his 1971 patent, marked the initial step toward anisotropic etching by leveraging plasma-generated reactive species to remove material selectively. Building on these foundations, evolved to address the limitations of isotropic wet processes, which undercut patterns and limited resolution in fabrication. By the early 1970s, researchers explored biased configurations to enhance directionality through bombardment, paving the way for more precise pattern transfer. The term "reactive ion etching" (RIE) was coined in the mid-1970s to specifically denote these processes, where chemically reactive are generated under low pressure, and the wafer is placed on a radio-frequency (RF)-powered to accelerate ions perpendicularly toward the surface. Around 1975, a surge of patents—approximately a dozen worldwide—formalized RIE systems, highlighting their role in transitioning from non-directional etches to controlled, -driven techniques that enabled finer feature sizes. These early inventions emphasized parallel-plate reactors for generation and reactive gas flows, allowing for the of dielectrics, metals, and polysilicon with improved . In its nascent applications, RIE was adopted in the for critical pattern delineation in device fabrication, replacing wet chemical etches that produced undercutting and poor edge definition due to their isotropic nature. This shift facilitated the production of higher-density circuits by enabling vertical sidewalls and sub-micron features, fundamentally advancing precision.

Evolution and Key Variants

In the , magnetically enhanced reactive ion etching (MERIE) emerged as a significant advancement, incorporating magnetic fields to confine electrons and increase density, which resulted in higher etch rates on the order of micrometers per minute and improved uniformity across wafers compared to conventional RIE systems. This technique, appealing for its ability to achieve high densities with low bias voltages, reduced damage while enhancing throughput for patterning features in the micrometer to sub-micrometer range, supporting the scaling demands of . The mid-1990s saw the invention of deep reactive ion etching (DRIE), also known as the Bosch process, by Franz Laermer and Andrea Urban at Robert Bosch GmbH, which utilized cyclic processes alternating SF6 for isotropic etching and O2 for passivation to achieve high-aspect-ratio features with vertical sidewalls and minimal scalloping. This innovation enabled the fabrication of deep, precise microstructures essential for microelectromechanical systems (MEMS), such as accelerometers and pressure sensors, revolutionizing high-volume production in automotive and consumer electronics. In the , the integration of with RIE (ICP-RIE) allowed for independent control of plasma density via inductive power (typically 1750–2500 W) and via power (25–300 W), facilitating high-density plasmas at low pressures (0.2–10 ) and enabling anisotropic etching of challenging materials like with rates up to 487 nm/min and selectivities exceeding 80:1. This development improved reproducibility and precision for non-planar microstructures in devices, including Schottky diodes and components. Post-2010 advancements include cryogenic RIE (Cryo DRIE), which operates at temperatures of −80 °C to −120 °C to enhance sidewall smoothness and achieve near-vertical profiles (up to 90.3°) with aspect ratios of 8:1 and etch rates of 3–4 μm/min, proving particularly valuable for ultra-precise nanotechnology applications in MEMS fabrication. Concurrently, improvements in etch selectivity for 3D NAND and advanced nodes have focused on plasma pulsing and novel chemistries, such as hydrogen fluoride with additives like phosphorus trifluoride, doubling etch rates to 640 nm/min while maintaining high selectivity (e.g., 10:1 or better) through over 200 oxide-nitride layers, addressing challenges in deep, narrow channels for denser memory structures as of 2025.

Fundamentals

Basic Principles

Reactive-ion etching (RIE) is a technique that utilizes a chemically reactive generated under conditions to remove material from substrates, such as wafers used in fabrication. The process occurs in a low-pressure environment, typically between 0.1 and tens of Pa, where reactive gases are ionized to form a containing species like radicals, ions, and electrons that interact with the surface. This method combines chemical , driven by reactive neutral species such as radicals that form volatile compounds with the material, and physical etching via transfer from accelerated s bombarding the surface. The between these chemical and physical components—first demonstrated experimentally in the late —enables etch rates far exceeding those achievable by either alone, allowing for controlled material removal. Unlike isotropic wet etching, which proceeds uniformly in all directions and leads to undercutting of features, RIE produces highly anisotropic profiles due to the directional of ion impacts, facilitating the fabrication of high-aspect-ratio structures essential for . In a typical RIE setup, the is sustained by applying radio-frequency (RF) power, often at 13.56 MHz, between parallel in the , which dissociates the feed gas into reactive . The is positioned on the powered (biased) , creating a self-bias voltage that accelerates positive ions toward the surface primarily in the direction normal to it, promoting vertical while minimizing lateral spread. This configuration distinguishes RIE from purely chemical , where the is not biased, resulting in less directional control. Central to evaluating RIE performance are several key parameters: the etch rate, defined as the volume or thickness of material removed per unit time (e.g., in ); selectivity, the of the etch rate of the target material to that of or adjacent layers, which ensures preservation of underlying structures (often >10:1 for over ); and , often defined as A = 1 - (lateral etch rate / vertical etch rate), approaching 1 for directionality, or equivalently the of vertical to lateral etch rates approaching . These metrics are influenced by variables like RF power, pressure, and gas composition, and their optimization is critical for achieving precise pattern transfer in device manufacturing.

Physics and Chemistry

Reactive-ion etching (RIE) relies on the generation of a low-pressure , typically sustained by radio-frequency (RF) power at 13.56 MHz, to ionize etching gases such as CF₄ or SF₆. This occurs in a capacitively coupled configuration at pressures ranging from 1 to 100 mTorr, where electrons accelerated by the RF collide with gas molecules, producing reactive radicals (e.g., atoms) and positive ions through and processes. The maintains a quasi-neutral bulk region, with electron densities around 10¹⁰ to 10¹¹ cm⁻³, enabling sustained reactive generation without significant thermal effects on the . The chemical aspect of RIE involves surface reactions driven by neutral radicals, which adsorb onto the substrate and form volatile compounds that desorb readily. For instance, fluorine radicals react with silicon to produce SiF₄, a gas with a low boiling point of -86°C, facilitating isotropic chemical etching in the absence of directional influences. Ion-enhanced desorption, however, promotes anisotropy by activating surface bonds and aiding the removal of reaction products, particularly in polymerizing chemistries where non-volatile residues might otherwise inhibit etching. These reactions are exothermic and proceed via Langmuir-Hinshelwood mechanisms, where adsorbed species interact on the surface. Physical sputtering in RIE arises from the bombardment of the by accelerated positive s, which gain kinetic energies of 100-500 as they traverse the plasma —a thin, non-neutral region near the powered where the directs s perpendicularly toward the surface. Momentum transfer from these s ejects surface atoms through direct collisions, contributing to of materials resistant to chemical attack and enhancing overall rates in processes. The physics, governed by Child-Langmuir law approximations, ensures ion directionality, with ion densities around 10¹⁵ cm⁻² s⁻¹, though at higher pressures can broaden angular distributions. Surface charging effects in RIE emerge from differential collection of charged species on insulating or patterned features, leading to distortions in local . In high-aspect-ratio trenches, differential charging causes trajectory deflection, resulting in where ions accumulate laterally at the base, eroding sidewalls nonuniformly. Micromasking occurs when charging promotes redeposition of non-volatile byproducts or erosion products onto the surface, creating localized etch-resistant spots that propagate defects. These phenomena are exacerbated in high-density s and can be mitigated by process tuning, but they highlight the interplay between plasma nonuniformity and surface .

Equipment

Core Components

The core components of a reactive-ion etching (RIE) system form the foundational necessary for generating and sustaining a low-pressure environment, enabling precise control over processes through maintenance, handling, gas introduction, and regulation. These elements ensure isolation from atmospheric contaminants, uniform distribution, and safe handling of reactive gases, with designs optimized for and applications. The serves as the primary enclosure where the is confined and the occurs. Typically constructed from or anodized aluminum to withstand corrosive etchants and maintain structural integrity under , it features a cylindrical with diameters ranging from 20 to 50 cm to accommodate wafers up to 200 mm or smaller substrates. Essential ports are integrated for pumping, gas inlets, and electrical feedthroughs, allowing connection to ancillary systems while minimizing leaks. The chamber operates at a base pressure of approximately 10^{-6} to eliminate residual gases and contaminants before process initiation, ensuring high-purity conditions for reproducible . The platter, or lower , holds and positions the during , functioning as the RF-biased component that accelerates toward for anisotropic . This is typically a flat, conductive capable of securing wafers via electrostatic chucking or clamping, with RF power applied at 13.56 MHz to generate the self-bias voltage essential for ion . is integrated through cooling channels or heaters, maintaining temperatures between 20°C and 100°C to manage reaction kinetics, prevent thermal damage, and optimize etch selectivity—for instance, backside cooling is often employed to dissipate heat from the . The gas delivery system introduces process gases into the chamber with high precision to form the reactive . It relies on mass flow controllers (MFCs) to regulate flows of etchants and additives, typically in the range of 10 to 100 standard cubic centimeters per minute (sccm), ensuring stable plasma chemistry and uniform . For example, (SF_6) is commonly used as the primary etchant for at flows of 10–100 sccm, while oxygen (O_2) is added at similar rates to promote passivation layers that enhance sidewall protection and control. These controllers, often equipped with digital feedback, allow real-time adjustments to gas mixtures, preventing over- or residue buildup. Vacuum pumps are critical for evacuating the chamber to the required low pressures and removing etching byproducts during . Turbomolecular pumps, often backed by roughing pumps, are standard for achieving and sustaining base pressures below 10^{-6} , providing high pumping speeds for inert and reactive gases. Cryogenic pumps serve as an alternative in contamination-sensitive setups, offering superior capture of and hydrocarbons through surface adsorption. valves, typically or gate types, regulate conductance between the chamber and pump, dynamically maintaining process pressures (e.g., 10–100 mTorr) despite varying gas loads. This combination ensures efficient byproduct evacuation, minimizing chamber contamination and enabling consistent .

System Types

Reactive-ion etching (RIE) systems are designed with varying architectures to optimize generation, , and , addressing limitations such as low density and poor uniformity in simpler setups. These variations enable independent control of density and energy, which is crucial for advanced processes. The parallel-plate RIE, also known as a (CCP) system, features two parallel within a , where radiofrequency (RF) power is applied to one to generate between them. This simple design achieves densities of approximately 10^9 to 10^10 /cm³, operating at pressures of 10–100 mTorr and RF frequencies around 13.56 MHz. While cost-effective and suitable for basic anisotropic through bombardment, it suffers from coupled control of density and , leading to potential non-uniformity and higher damage risks at elevated powers. Inductively coupled plasma (ICP) RIE systems incorporate a separate RF , typically helical or planar, surrounding the chamber to inductively couple power into the , decoupling plasma generation from substrate . This allows for higher plasma densities of 10^11 to 10^12 ions/cm³ at lower pressures (1–10 mTorr), independent adjustment of ion and for improved etch uniformity and rates. ICP designs are scalable for larger wafers and widely adopted for high-aspect-ratio features, though they require more complex power delivery systems. Electron cyclotron resonance (ECR) RIE employs microwave power at 2.45 GHz combined with a (typically 875 Gauss) to sustain via , often in a separate region from the . Operating at very low pressures (<1 mTorr), it generates densities up to 10^12 ions/cm³, promoting highly directional etching with reduced ion bombardment damage due to lower bias voltages. ECR systems excel in precision applications but involve intricate magnetic components, increasing maintenance demands. Triode and remote plasma RIE configurations enhance directionality by adding a third electrode (triode) or generating plasma remotely from the substrate (remote), minimizing direct exposure to charged species. Triode systems decouple plasma excitation from biasing for better energy control, while remote setups transport neutral radicals downstream, reducing charging effects at densities varying from 10^10 to 10^11 ions/cm³. These are particularly useful in deep etching variants, such as the , which alternates etching and passivation cycles in ICP-based triode-like setups for high-aspect-ratio silicon structures.

Operation

Process Steps

The reactive-ion etching (RIE) process begins with substrate preparation in a cleanroom environment to ensure contamination-free conditions. The substrate, typically a , is cleaned using wet chemical methods such as or to remove organic residues and particles. A masking layer, such as or a hard mask like , is then applied and patterned via to define the areas for etching. Following preparation, the substrate is loaded into the RIE chamber, which is evacuated to a base pressure of approximately 10^{-6} Torr using a turbomolecular or mechanical pump to remove residual gases and achieve a high-vacuum environment. The process gas mixture, often including fluorinated compounds like or for silicon etching, is then introduced at controlled flow rates to reach an operating pressure of 10-100 mTorr. Plasma ignition occurs by applying radio-frequency (RF) power, typically in the range of 100-1000 W at frequencies like 13.56 MHz, to the electrodes, ionizing the gas and generating a reactive plasma. The plasma is allowed to stabilize for 1-5 minutes to ensure uniform conditions, with the substrate often placed on the powered electrode to induce a self-bias for ion acceleration. During the etching phase, the process is maintained for 1-30 minutes, depending on the desired etch depth, with ions from the plasma bombarding the substrate surface to remove material selectively. Conditions such as gas flow, pressure, and RF power are held constant to achieve the targeted profile. Upon reaching the endpoint, the RF power is turned off, and the chamber is purged with inert gas to remove residual reactive species. Endpoint detection is commonly performed using optical emission spectroscopy (OES), which monitors changes in plasma emission lines—such as a drop in silicon-related signals—to precisely halt the etch and prevent over-etching. The substrate is then removed for post-processing, including mask stripping and inspection.

Etching Mechanisms

Reactive-ion etching (RIE) involves a combination of chemical and physical processes that enable precise material removal from substrates, primarily through the interaction of plasma-generated species with the surface. The primary mechanisms include ion-assisted chemical etching, physical sputtering, sidewall passivation for anisotropy, and inherent selectivity based on material properties. These processes occur simultaneously under the influence of the plasma's electric field, which directs ions perpendicular to the substrate, enhancing directional etching compared to isotropic wet methods. In ion-assisted chemical etching, energetic ions bombard the surface to break chemical bonds, facilitating reactions between reactive radicals and the substrate to form volatile byproducts that are easily removed. For instance, in a CF₄ plasma, fluorine radicals (F) react with silicon (Si) to form SiF₄, but the reaction rate is significantly enhanced by ion impact, which disturbs the surface and increases the probability of radical adsorption and product desorption. This synergy can increase etch rates by orders of magnitude compared to pure chemical etching, as demonstrated in early studies where ion bombardment lowered the activation energy for halogen-surface reactions. Physical ion milling, or sputtering, contributes to material removal through direct momentum transfer from vertically incident ions, dislodging atoms from the surface without relying on chemical reactions. This mechanism is prominent in areas without chemical reactivity or when ion energies exceed 100 eV, leading to V-shaped groove profiles in unmasked regions due to the angular distribution of sputtered atoms. While less dominant in reactive chemistries, sputtering enhances overall etch rates and anisotropy by preferentially removing material at the bottom of features, where ion flux is highest. Sidewall passivation plays a crucial role in achieving anisotropic etching by depositing thin polymer films on lateral surfaces, inhibiting chemical attack while allowing vertical etching to proceed. Additives like in fluorocarbon plasmas dissociate to form fluorocarbon radicals that polymerize on sidewalls, forming a protective layer that is removed more slowly than the substrate material due to reduced ion flux at non-perpendicular angles. This enables high aspect ratios exceeding 10:1 in deep features, as the passivation layer prevents undercutting and maintains straight sidewalls. Etch selectivity in RIE arises from differences in bond energies, surface reactivity, and passivation behavior between materials, allowing preferential removal of one layer over another. For example, in fluorocarbon s, SiO₂ exhibits high selectivity over Si (>10:1) because oxygen atoms released from SiO₂ scavenge carbon from the , forming or CO₂ and preventing deposition on the surface, while Si accumulates carbon-rich films that inhibit radical access. This mechanism exploits the chemical dissimilarity, enabling precise pattern transfer in multilayer structures.

Applications

Microelectronics and Semiconductors

Reactive-ion etching (RIE) plays a pivotal role in microelectronics and semiconductor fabrication, particularly in the precise patterning required for integrated circuit production. It enables the transfer of photolithographic patterns into device structures through anisotropic etching, which is essential for achieving the high fidelity needed in complementary metal-oxide-semiconductor (CMOS) processes. This capability supports the creation of intricate features such as gates, contacts, and trenches, allowing for device scaling to sub-10 nm dimensions while maintaining structural integrity and performance. In CMOS manufacturing, RIE is widely employed for pattern transfer during the front-end-of-line (FEOL) stages, where it etches gates, source/drain contacts, and isolation trenches to define architectures. For instance, (DRIE) techniques within RIE processes fabricate vertical nanowires with diameters as small as 30 nm for gate-all-around (GAA) MOSFETs, ensuring smooth sidewalls and compatibility with high-k dielectrics. Similarly, RIE patterns sub-10 nm fin widths in self-aligned InGaAs FinFETs, followed by of high-k gate stacks, which enhances gate control and reduces leakage in advanced nodes. These applications leverage RIE's directionality to achieve aspect ratios exceeding 10:1, critical for trenches in FinFETs and nanosheet devices below 10 nm. For back-end-of-line (BEOL) interconnects, RIE facilitates selective etching of low-k dielectrics to form vias and metal lines in processes, minimizing damage to porous materials like SiCOH (k ≈ 2.2–3.0). This selectivity ensures clean via profiles and prevents plasma-induced , which is vital for maintaining in multilayer Cu interconnect stacks at nodes like 7 nm and beyond. RIE patterning in these flows integrates with liner deposition and , addressing challenges such as seed continuity in high-aspect-ratio features. Beyond logic devices, RIE contributes to photovoltaic applications within processing, notably by texturing multicrystalline surfaces for solar cells. Using SF₆/O₂ chemistries, maskless RIE creates random nanostructures that reduce surface reflectivity to as low as 6% for n-type , enhancing light trapping and short-circuit . A 2011 study demonstrated that doping levels in influence etching rates and cone formation in SF₆/O₂ s, leading to textured surfaces with improved antireflection properties. In advanced nodes as of , RIE is integral to EUV-integrated flows for FinFET and GAA fabrication, particularly in high-k/metal gate stacks like HfO₂/TiN. For stacked nanosheet GAA devices, RIE defines multilayer Si/SiGe channels post-EUV patterning, enabling precise release etches and gate wrapping around sub-10 nm sheets while integrating with self-aligned quad patterning. This supports multi-Vt options and scalability to 2 nm nodes, where RIE's control over sidewall profiles mitigates variability in high-k interfaces, including selective for backside delivery networks. The anisotropic nature of RIE further aids in achieving verticality essential for these structures.

MEMS and Other Fields

Reactive-ion etching (RIE) plays a pivotal role in microelectromechanical systems () fabrication, particularly for creating deep trenches and structural releases essential to inertial sensors such as accelerometers and gyroscopes. The (DRIE) variant of RIE enables the production of high-aspect-ratio features, often exceeding 50:1, which is critical for achieving precise mechanical suspensions and cavities in these devices. For instance, DRIE processes have been optimized to etch trenches up to 120 μm deep with minimal sidewall scalloping, ensuring structural integrity and performance in vibration-sensitive applications. This capability supports the release of suspended microstructures, allowing for the fabrication of compact, high-sensitivity sensors used in automotive stability control and . In (GaAs) monolithic integrated circuits (MMICs), RIE is employed to etch via-hole grounds that provide low-inductance connections to the backside metallization, enhancing high-frequency performance. These vias, typically 100–200 μm deep, are formed using chemistries like CCl₂F₂/CCl₄ to achieve anisotropic profiles and smooth sidewalls, reducing parasitic effects in amplifiers and switches. Studies from the late 2000s demonstrated that such RIE processes enable reliable grounding in GaAs substrates up to 200 μm thick, improving power handling and in radar and communication systems. This application underscores RIE's versatility in compound semiconductors beyond silicon-based . RIE extends to nanotechnology, where it facilitates the patterning of nanostructures in materials like and for quantum devices. In , inductively coupled plasma-RIE (ICP-RIE) techniques pattern color-center hosting membranes and nanowires with nanoscale precision, enabling scalable integration into quantum sensing and computing platforms. For , RIE-based etching creates defined edges and pores, supporting the fabrication of arrays and spintronic elements with controlled electronic properties. These methods achieve sub-100 nm features while preserving material integrity, as evidenced in hybrid photonics for quantum repeaters. Beyond these, RIE finds applications in optical through the of waveguides in SiO₂, where selective processes minimize losses for integrated photonic circuits. Fluorocarbon-based RIE yields smooth, vertical sidewalls in SiO₂ layers, supporting low-loss propagation in wavelengths for devices like modulators and couplers. In biomedical fields, RIE microfluidic channels in polymers such as PMMA, enabling bio-MEMS for and point-of-care diagnostics; as of 2025, trends emphasize hybrid polymer-silicon platforms for implantable sensors with enhanced .

Advantages and Limitations

Key Benefits

Reactive-ion etching (RIE) offers high , resulting in vertical etch profiles with minimal undercutting, which enables the fabrication of sub-micron features that are challenging with isotropic wet methods. This directionality arises from the acceleration of ions through the at near-normal incidence to the surface, providing precise control over feature dimensions in processes. RIE also provides excellent selectivity, with ratios reaching up to 100:1 or higher for specific material pairs, such as to , thereby preserving underlying masks and layers during etching. This capability is enhanced by tailored plasma chemistries, like fluorine-deficient plasmas, which promote selective deposition on non-target surfaces. As a dry process, RIE eliminates liquid waste associated with wet etching, improves compatibility with masks that may degrade in aqueous environments, and supports scalability for large-area production in . It generates reactive species unavailable in standard gas bottles, operating at temperatures that avoid thermal damage to sensitive substrates. Established as a mature technology since the , with initial patents filed around 1975, RIE demonstrates high in industrial settings, achieving etch rate uniformity below 5% across wafers through symmetrical chamber designs and precise process control. This low variability ensures consistent results from die-to-die and wafer-to-wafer, making it a cornerstone for reliable high-volume production.

Challenges and Drawbacks

One significant challenge in reactive-ion etching (RIE) is plasma-induced damage, where high-energy bombardment during the etching process can create lattice defects, charge buildup, and contamination in underlying substrates. This damage is particularly problematic for sensitive materials like (GaAs), where it leads to reduced carrier mobility and degraded device performance in structures such as MESFETs. In silicon-based devices, such effects manifest as increased junction leakage currents or elevated due to the formation of a damaged surface layer. Studies have shown that these issues arise primarily from the applied bias voltage and ion flux, exacerbating defects in thin gate oxides or high-mobility channels. RIE processes are highly sensitive to operational parameters, with etch rates exhibiting significant variation in response to even in chamber , RF power, or gas flow. For instance, increasing ICP source power enhances reactive species concentration, thereby boosting etch rates in materials like , but small changes can inversely reduce rates in polymers such as SU-8. This parameter dependence necessitates rigorous calibration and real-time to maintain uniformity and , as deviations can lead to over-etching or incomplete transfer. Such sensitivity complicates scaling for high-volume production, requiring advanced control systems to mitigate inconsistencies. The equipment for RIE involves substantial costs and operational complexity due to the need for high-vacuum systems, RF matching networks, and integration within environments. Vacuum pumps and plasma generation components demand regular maintenance to prevent and ensure , with initial setup costs often exceeding those of wet etching alternatives. In fabrication, these systems require dedicated infrastructure to avoid particle-induced defects, further elevating expenses and limiting accessibility for smaller research facilities. High-aspect-ratio etching tools, such as those using the Bosch process, amplify this complexity through multi-step cycling and precise alignment needs. Environmental concerns arise from the use of like CF4 in RIE, which are potent gases with potentials (GWPs) of around 6,650 over 100 years, contributing to emissions during and chamber cleaning in manufacturing. These perfluorocarbons (PFCs) and alternatives like NF3 (GWP of 17,200) account for a significant portion of industry GHG emissions, prompting regulatory actions such as the EU's F-gas (EU) 2024/573, which entered into force in March 2024 and imposes phasedown targets reducing HFC and PFC placement on the market by up to 79% by 2030, with stricter controls effective from 2025. In response, the sector is shifting toward lower-GWP alternatives and abatement technologies to comply with these standards while maintaining efficacy.

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