首页> 外文会议>Advances in Resist Technology and Processing XII >Aminodisilanes as silylating agents for dry-developed positive-tone resists for deep-ultraviolet (248-nm) and extreme ultraviolet (13.5-nm) microlithography
【24h】

Aminodisilanes as silylating agents for dry-developed positive-tone resists for deep-ultraviolet (248-nm) and extreme ultraviolet (13.5-nm) microlithography

机译:氨基硅烷作为硅烷化剂,用于干法开发的用于深紫外(248 nm)和远紫外(13.5 nm)微光刻的正性抗蚀剂

获取原文

摘要

Abstract: Disilanes are used as silylating reagents for near-surface imaging with deep-UV (248 nm) and EUV (13.5 nm) lithography. A relatively thin imaging layer of a photo-cross-linking resist is spun over a thicker layer of hard-baked resist that functions as a planarizing layer and antireflective coating. Photoinduced acid generation and subsequent heating crosslinks render exposed areas impermeable to an aminodisilane that reacts with the unexposed regions. Subsequent silylation and reactive ion etching affords a positive-tone image. The use of disilanes introduces a higher concentration of silicon into the polymer than is possible with silicon reagents that incorporate only one silicon atom per reactive site. The higher silicon content in the silylated polymer increases etching selectivity between exposed and unexposed regions and thereby increases the contrast. The synthesis and reactivity of `smaller' disilanes, N,N-dimethylamino-1,2-dimethyldisilane, (DMADMDS), and N,N-diethylamino-1,2- dimethyldisilane also are described. Additional silylation improvements that minimize flow during silylation also are discussed including the addition of bifunctional disilanes to the monofunctional DMAPMDS. This causes the crosslinking to occur during silylation which minimizes flow. We have resolved high aspect ratio, very high quality 0.20 $mu@m line and space patterns at 248 nm with a stepper having a numerical aperture (NA) $EQ 0.53 and have resolved $LSEQ 0.15 $mu@m line and spaces at 13.5 nm. !24
机译:摘要:用Diell-uV(248nm)和EUV(13.5nm)光刻用作近表面成像的含甲硅烷基的试剂。光交联抗蚀剂的相对薄的成像层在用作平坦层和抗反射涂层的较厚层上旋转。光突出的酸产生和随后的加热交联通过与未曝光区域反应的氨基二硅烷不可渗透的暴露区域。随后的甲硅烷基化和反应离子蚀刻提供正色调图像。使用硅酸钠将较高浓度的硅含入聚合物中,而不是硅试剂,其仅掺入每个反应性位点的一个硅原子。甲硅烷基化聚合物中的较高的硅含量增加了暴露和未曝光区域之间的蚀刻选择性,从而增加对比度。还描述了“较小”硅酸钠,N,N-二甲基氨基-1,2-二甲基二硅烷,(DMADMDS)和N,N-二乙基氨基-1,2-二甲基二硅烷的合成和反应性。还讨论了额外的甲硅烷基化改善,其在甲硅烷基化过程中最小化的流动,包括向单官能DMAPMD添加双官能硅酸盐。这使得在甲硅烷基化期间发生交联,其最小化流动。我们已经解决了高纵横比,非常高质量的0.20 $ MU @ M线和空间图案,在248nm时,步进具有数值孔径(NA)$ EQ 0.53,并在13.5时已解决$ LSEQ 0.15 $ MU @ M线和空格纳米。 !24

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号