2006
DOI: 10.1039/b514146j
|View full text |Cite
|
Sign up to set email alerts
|

Molecular glass photoresists for advanced lithography

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
81
0

Year Published

2007
2007
2013
2013

Publication Types

Select...
4
4
1

Relationship

1
8

Authors

Journals

citations
Cited by 85 publications
(82 citation statements)
references
References 35 publications
1
81
0
Order By: Relevance
“…[ 90 ] In general the molecular glass resist has a well-defi ned small-molecule core that bears protected base-soluble groups (such as hydroxyls and carboxyls) as shown in Figure 21b . With this approach the core chemistry can vary from calix [4]resorcinarenes (ringlike), [91][92][93] branched phenolic groups, [ 94,95 ] and hexaphenolic groups (disklike). [ 96,97 ] Early approaches with molecular resists led to low glass-transition temperatures, however, such problems were resolved by increased hydrogen bonding functionality and the design of the core structure.…”
Section: Advances By Materials Structurementioning
confidence: 99%
“…[ 90 ] In general the molecular glass resist has a well-defi ned small-molecule core that bears protected base-soluble groups (such as hydroxyls and carboxyls) as shown in Figure 21b . With this approach the core chemistry can vary from calix [4]resorcinarenes (ringlike), [91][92][93] branched phenolic groups, [ 94,95 ] and hexaphenolic groups (disklike). [ 96,97 ] Early approaches with molecular resists led to low glass-transition temperatures, however, such problems were resolved by increased hydrogen bonding functionality and the design of the core structure.…”
Section: Advances By Materials Structurementioning
confidence: 99%
“…These properties, however, have been found to be inversely related, a relationship commonly referred to as the RLS trade-off [1]. To overcome the RLS trade-off, the lithographic community is investigating alternative resist platforms such as molecular glasses [2][3][4], polymer-bound photoacid generators (PAGs) [5][6][7], and chain-scission polymers [8][9][10][11][12][13][14][15][16][17][18][19][20][21].…”
Section: Introductionmentioning
confidence: 99%
“…The resulting cross-linked oligomers are insoluble in aqueous base, thus providing the solubility switch required for development. This system is capable of producing 60 nm line/space patterns (Yang et al, 2006). (2), and photoacid generator (3) (Yang et al, 2006).…”
Section: Molecular Glass Photoresistsmentioning
confidence: 99%
“…This system is capable of producing 60 nm line/space patterns (Yang et al, 2006). (2), and photoacid generator (3) (Yang et al, 2006).…”
Section: Molecular Glass Photoresistsmentioning
confidence: 99%