TY - JOUR
T1 - Eliminating the Tg-Confinement Effect in Polystyrene Films
T2 - Extraordinary Impact of a 2 mol % 2-Ethylhexyl Acrylate Comonomer
AU - Wang, Tong
AU - Hu, Sumeng
AU - Zhang, Sipei
AU - Peera, Asghar
AU - Reffner, John
AU - Torkelson, John M.
N1 - Funding Information:
This research was supported by the University Partnership Initiative between Northwestern University and The Dow Chemical Company and by discretionary funds from a Walter P. Murphy Professorship (J.M.T.). This research made use of the IMSERC NMR and the MS Facility at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-2025633), the State of Illinois, International Institute for Nanotechnology (IIN) and Northwestern University.
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/11/8
Y1 - 2022/11/8
N2 - Nanoconfined polystyrene (PS) films exhibit substantial reductions in glass transition temperature (Tg) from bulk Tg. By incorporating 2−6 mol % 2-ethylhexyl acrylate (EHA) into styrene (S)-based random copolymers and characterization via ellipsometry, we show that the Tg-confinement effect for films supported on silicon wafers is eliminated within experimental uncertainty down to a 15 nm thickness. Previous studies have neutralized this confinement effect by the copolymerization of minority levels of styrene with majority levels of a comonomer that can undergo hydrogen bonding with hydroxyl groups on a substrate surface, thus counteracting the free-surface-based Tg reduction with a Tg increase near the substrate interface. In contrast, the Tg-confinement effect is eliminated in our 2−6 mol % EHA copolymers independent of the presence of substrate surface hydroxyl groups. Thus, polymer−substrate interfacial hydrogen bonds play no significant role in neutralizing the Tg-confinement effect in the S-based copolymers with 2−6 mol % EHA. Instead, the neutralization must come from suppressing free-surface effects via very low levels of an EHA monomer in the copolymer. Importantly, this simple approach to eliminate the Tg-confinement effects with as little as 2 mol % EHA is accompanied by only a minor change in bulk Tg and no change in thermal expansivity within the experimental error relative to PS. Furthermore, this approach cannot be generalized to other acrylate comonomers, such as n-butyl acrylate. It neither requires complex syntheses to achieve dense brush, bottlebrush, or cyclic or ring polymer topologies nor the addition of a plasticizer or a surfactant to the polymer, earlier approaches that suppressed the Tg-confinement effect in PS. For a 99:1 mol % S/EHA copolymer, the confinement effect is nearly identical to that of PS, indicating that a critical yet low EHA level is needed to eliminate the effect.
AB - Nanoconfined polystyrene (PS) films exhibit substantial reductions in glass transition temperature (Tg) from bulk Tg. By incorporating 2−6 mol % 2-ethylhexyl acrylate (EHA) into styrene (S)-based random copolymers and characterization via ellipsometry, we show that the Tg-confinement effect for films supported on silicon wafers is eliminated within experimental uncertainty down to a 15 nm thickness. Previous studies have neutralized this confinement effect by the copolymerization of minority levels of styrene with majority levels of a comonomer that can undergo hydrogen bonding with hydroxyl groups on a substrate surface, thus counteracting the free-surface-based Tg reduction with a Tg increase near the substrate interface. In contrast, the Tg-confinement effect is eliminated in our 2−6 mol % EHA copolymers independent of the presence of substrate surface hydroxyl groups. Thus, polymer−substrate interfacial hydrogen bonds play no significant role in neutralizing the Tg-confinement effect in the S-based copolymers with 2−6 mol % EHA. Instead, the neutralization must come from suppressing free-surface effects via very low levels of an EHA monomer in the copolymer. Importantly, this simple approach to eliminate the Tg-confinement effects with as little as 2 mol % EHA is accompanied by only a minor change in bulk Tg and no change in thermal expansivity within the experimental error relative to PS. Furthermore, this approach cannot be generalized to other acrylate comonomers, such as n-butyl acrylate. It neither requires complex syntheses to achieve dense brush, bottlebrush, or cyclic or ring polymer topologies nor the addition of a plasticizer or a surfactant to the polymer, earlier approaches that suppressed the Tg-confinement effect in PS. For a 99:1 mol % S/EHA copolymer, the confinement effect is nearly identical to that of PS, indicating that a critical yet low EHA level is needed to eliminate the effect.
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U2 - 10.1021/acs.macromol.2c01917
DO - 10.1021/acs.macromol.2c01917
M3 - Article
AN - SCOPUS:85141604995
SN - 0024-9297
VL - 55
SP - 9601
EP - 9611
JO - Macromolecules
JF - Macromolecules
IS - 21
ER -