Metal oxide resists (MORs) have become one of the most attractive photoresist platforms that allow for high resolution and etch bias of small features while having a robust lithography performance. In this work, we present our study about improving line fidelity and reducing the dose of MOR for line space EUV lithography by applying spin-on underlayers (ULs). It is known that MOR patterning is induced by the activation during exposure and condensation of the active sites. Herein, we discuss the influence of ULs on MOR performance. A series of ULs with various chemistry, thickness, or process conditions were screened with MOR using NXE3400 EUV exposure system to print 14-nm HP line-space features. The results show that the nanobridges and scum can be alleviated, while the remaining resist thickness after development can be improved by up to 20% along with 5 to 10% dose reductions. A comprehensive assessment of the ULs encompassing various chemistries examines coating quality, uniformity, and surface energy. The discussion delves into the correlation between the surface properties including morphology, interaction, etc., and their respective impacts on lithography performance. Lastly, some spin-on ULs produce up to 75% reduction of metal diffusion from the MOR into the underlying layers.
Spin-on glass (SOG) underlayers to enhance extreme ultraviolet (EUV) lithography for patterning below 28-nm pitch require an in-depth understanding of the required adhesion forces necessary for good lithography. Here, we proposed a fundamentally new SOG underlayer platform composed of polymer blends that can achieve superior uniformity to improve line fidelity and provide a design path for underlayer materials. The structure and property of elemental composition and surface energy can be controlled easily and precisely by varying the combination of polymer, and consequently understanding and tuning the lithographic performance. The lithographic performance of SOG blends was evaluated using NXE3400 EUV exposure system to print 13-nm and 14-nm HP line-space features and contact hole features with CD of 20-nm. The results show that the polymer blends expand the process window for EUV resist for line-space with printable CD >11 nm and biased LWR to 3.6-nm without impact on dose when compared to conventional copolymers. In the case of CH patterning, CDU and DOF improvements were observed when compared to conventional SOG copolymers. Systematic studies on polymer blends based on functional groups and formulation compositions are in progress to establish a better understanding of enhancement of EUV lithography.
A large screening of underlayer materials for extreme ultraviolet lithography is reported in this work. The main motivation for the screening of functional materials lies in the search for dose reduction and defect mitigation. Some promising results shown in here prove that the usage of functionalized underlayers and primers improves the pattern quality without adding to the complexity of litho processing.
Directed self-assembly (DSA) of block copolymers (BCPs) is one of the most promising patterning technologies for future lithography nodes. However, one of the biggest challenges to DSA is the pattern transfer by plasma etching from BCP to hardmask (HM) because the etch selectivity between BCP and neutral brush layer underneath is usually not high enough to enable robust pattern transfer. This paper will explore the plasma etch conditions of both BCPs and neutral brush layers that may improve selectivity and allow a more robust pattern transfer of DSA patterns into the hardmask layer. The plasma etching parameters that are under investigation include the selection of oxidative or reductive etch chemistries, as well as plasma gas pressure, power, and gas mixture fractions. Investigation into the relationship between BCP/neutral brush layer materials with varying chemical compositions and the plasma etching conditions will be highlighted. The culmination of this work will demonstrate important etch parameters that allow BCPs and neutral brush layers to be etched into the underlying hardmask layer with a large process window.
High-χ block copolymers for directed self-assembly (DSA) patterning that do not need topcoat or solvent annealing have been developed. A variety of functionalities have been successfully added into the block copolymers, such as balanced surface energy between the polymer blocks, outstandingly high χ, tunable glass transition temperature (Tg), and selective crosslinking. Perpendicular orientation control, as desired for patterning, of the block copolymers can be simply achieved by thermal annealing due to the equal surface energy of the polymer blocks at the annealing temperatures, which allows avoiding solvent annealing or top-coat. The χ value can be tuned up to achieve L0 as low as 8-10 nm for lamellar-structured block copolymers and hole/pillar size as small as 5-6 nm for cylinder-structured block copolymers. The Tg of the block copolymers can be tuned to improve the kinetics of thermal annealing by enhancing the polymer chain mobility. Block-selective crosslinking facilitates the pattern transfer by mitigating pattern collapse during wet etching and improving oxygen plasma etching selectivity between the polymer blocks. This paper provides an introductory review of our high-χ block copolymer materials with various functionalities for achieving improved DSA performance.
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