TY - JOUR
T1 - Pressure-Sensitive Adhesive with Enhanced and Phototunable Underwater Adhesion
AU - Zhou, Yongsen
AU - Zhang, Chao
AU - Gao, Shouwei
AU - Li, Wanbo
AU - Kai, Ji Jung
AU - Wang, Zuankai
N1 - Funding Information:
The authors would like to acknowledge the financial support from Guangdong-Hong Kong Technology Cooperation Funding Scheme (GHP/021/19SZ), the Innovation and Technology Fund (9440248), the National Natural Science Foundation of China (No. 51975502), and the Research Grants Council of Hong Kong (No. C1006-20WF, CityU No. 11213320, CityU No. 11201020).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/10/27
Y1 - 2021/10/27
N2 - Pressure-sensitive adhesives (PSAs) are extensively used in diverse applications such as semiconductor manufacturing, labeling, and healthcare because of their quick and viscoelasticity-driven physical adhesion to dry surfaces. However, most of the existing PSAs normally fail to maintain or even establish adhesion under harsh conditions, particularly underwater, due to the lack of robust chemical functionalities for chemistry-based adhesion. Meanwhile, these PSAs are incapable of altering the adhesion in response to external stimuli, limiting their employment in applications requiring dynamic adhesion. Here, we develop a chemically functionalized PSA (f-PSA) with enhanced and phototunable underwater adhesion by incorporating an underwater adhesion enhancer (i.e., mussel-inspired catechol) and a photoresponsive functionality (i.e., anthracene) into a standard acrylic PSA matrix. The synergistic coupling of viscoelasticity-driven physical adhesion originating from the matrix with catechol-enabled chemical adhesion secures sufficient interfacial molecular interactions and leads to enhanced underwater adhesion. The efficient dimerization of anthracene via light-triggered cycloaddition facilely mediates the viscoelastic property of f-PSA, rendering the phototunable adhesion. We envision that this f-PSA can open up more opportunities for applications such as underwater manipulation, transfer printing, and medical adhesives.
AB - Pressure-sensitive adhesives (PSAs) are extensively used in diverse applications such as semiconductor manufacturing, labeling, and healthcare because of their quick and viscoelasticity-driven physical adhesion to dry surfaces. However, most of the existing PSAs normally fail to maintain or even establish adhesion under harsh conditions, particularly underwater, due to the lack of robust chemical functionalities for chemistry-based adhesion. Meanwhile, these PSAs are incapable of altering the adhesion in response to external stimuli, limiting their employment in applications requiring dynamic adhesion. Here, we develop a chemically functionalized PSA (f-PSA) with enhanced and phototunable underwater adhesion by incorporating an underwater adhesion enhancer (i.e., mussel-inspired catechol) and a photoresponsive functionality (i.e., anthracene) into a standard acrylic PSA matrix. The synergistic coupling of viscoelasticity-driven physical adhesion originating from the matrix with catechol-enabled chemical adhesion secures sufficient interfacial molecular interactions and leads to enhanced underwater adhesion. The efficient dimerization of anthracene via light-triggered cycloaddition facilely mediates the viscoelastic property of f-PSA, rendering the phototunable adhesion. We envision that this f-PSA can open up more opportunities for applications such as underwater manipulation, transfer printing, and medical adhesives.
KW - anthracene
KW - catechol
KW - pressure-sensitive adhesives
KW - tunable adhesion
KW - underwater adhesion
UR - http://www.scopus.com/inward/record.url?scp=85118148638&partnerID=8YFLogxK
U2 - 10.1021/acsami.1c16146
DO - 10.1021/acsami.1c16146
M3 - Journal article
C2 - 34652895
AN - SCOPUS:85118148638
SN - 1944-8244
VL - 13
SP - 50451
EP - 50460
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 42
ER -