Study of electron-induced chemical transformations in model resists

被引:0
|
作者
Mueller, Maximillian [1 ]
McAfee, Terry [2 ]
Naulleau, Patrick [2 ]
Oh, Dahyun [1 ]
Kostko, Oleg [2 ]
机构
[1] San Jose State Univ, San Jose, CA 95192 USA
[2] Lawrence Berkeley Natl Lab, Ctr Xray Opt, Berkeley, CA USA
关键词
secondary electrons; residual gas analysis (RGA); Fourier-transform infrared spectroscopy (FTIR); electron-induced chemistry; electron-gun exposure; outgassing; model photoresists; extreme ultraviolet lithography (EUV); EUV;
D O I
10.1117/12.2686929
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
In extreme ultraviolet (EUV) resists, due to the high energy of the incident photons, most of the radiation chemistry arises from the photon-generated primary and secondary electrons and not the EUV photons themselves. These electrons are generated by a cascade of inelastic scattering events, have a wide range of energies, and play a leading role in EUV patterning by initiating chemical transformations. To characterize electron-induced chemical transformations we exposed photoresist films to an electron beam 7-9 mm in diameter with energies varied from 20 to 80 eV to study the effect of fast primary electrons as well as slow secondary electrons on photoresist materials. Chemical changes of poly-tert-butyl methacrylate (tBMA), poly-methyl methacrylate (PMMA), and poly-4-hydroxystyrene (PHS) were characterized in-situ during exposure using a quadrupole residual gas analyzer (RGA). Full RGA spectra were used to identify the outgassed compounds from samples, and the time dependence of key chemical fragment masses was studied to observe the depletion of fragments from the sample over time. Transmission FTIR data were collected through exposed spots to quantify the changes in chemical bond structure. The number of molecules lost from each resist was estimated by the integrated partial pressure rise observed in RGA and compared to the total thickness change of exposed areas measured using ellipsometry.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Study of electron-induced chemical transformations in polymers
    Mueller, Maximillian
    Mcafee, Terry
    Naulleau, Patrick
    Oh, Dahyun
    Kostko, Oleg
    [J]. Journal of Micro/Nanopatterning, Materials and Metrology, 2024, 23 (04)
  • [2] Electron-induced crosslinking of aromatic self-assembled monolayers:: Negative resists for nanolithography
    Geyer, W
    Stadler, V
    Eck, W
    Zharnikov, M
    Gölzhäuser, A
    Grunze, M
    [J]. APPLIED PHYSICS LETTERS, 1999, 75 (16) : 2401 - 2403
  • [3] Low-Energy Electron-Induced Transformations in Organolead Halide Perovskite
    Milosavljevic, Aleksandar R.
    Huang, Weixin
    Sadhu, Subha
    Ptasinska, Sylwia
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (34) : 10083 - 10087
  • [4] Electron-induced fragmentation of water droplets: Simulation study
    Suchan, Jiri
    Kolafa, Jiri
    Slavicek, Petr
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2022, 156 (14):
  • [5] Evidence of hot electron-induced chemical degradation in electroluminescence spectra of polyethylene
    Teyssedre, Gilbert
    Laurent, Christian
    [J]. Journal of Applied Physics, 2008, 103 (04):
  • [6] Electron-induced chemistry of alcohols
    Ibanescu, Bogdan C.
    May, Olivier
    Monney, Angele
    Allan, Michael
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2007, 9 (24) : 3163 - 3173
  • [7] Electron-Induced Proton Transfer
    Matyushov, Dmitry, V
    Newton, Marshall D.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2021, 125 (44): : 12264 - 12273
  • [8] Evidence of hot electron-induced chemical degradation in electroluminescence spectra of polyethylene
    Teyssedre, Gilbert
    Laurent, Christian
    [J]. JOURNAL OF APPLIED PHYSICS, 2008, 103 (04)
  • [9] A study of electron beam-induced conductivity in resists
    Hwu, JJ
    Joy, DC
    [J]. SCANNING, 1999, 21 (04) : 264 - 272
  • [10] Crystallinity effect on electron-induced molecular structure transformations in additive-free PLA
    Zhang, Yinglan
    Mueller, Michael Thomas
    Boldt, Regine
    Stommel, Markus
    [J]. POLYMER, 2023, 265