Open AccessSuperhydrophobic‐Substrate‐Assisted Construction of Free‐Standing Microcavity‐Patterned Conducting Polymer Films
Author(s) -
Chen Yupeng,
Zhu Zhongpeng,
Jiang Xiangyu,
Jiang Lei
Publication year - 2021
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202100949
Subject(s) - materials science , bioelectronics , nanotechnology , substrate (aquarium) , polymer , polymerization , nanostructure , wetting , adhesion , composite material , biosensor , oceanography , geology
Abstract Patterned conducting polymer films with unique structures have promising prospects for application in various fields, such as actuation, water purification, sensing, and bioelectronics. However, their practical application is hindered because of the limitations of existing construction methods. Herein, a strategy is proposed for the superhydrophobic‐substrate‐assisted construction of free‐standing 3D microcavity‐patterned conducting polymer films (McPCPFs) at micrometer resolution. Easy‐peeling and nondestructive transfer properties are achieved through electrochemical polymerization along the solid/liquid/gas triphase interface on micropillar‐structured substrates. The effects of the wettability and geometrical parameters of the substrates on the construction of McPCPFs are systematically investigated in addition to the evolution of the epitaxial growth along the triphase interface at different polymerization times. The McPCPFs can be easily peeled from superhydrophobic surfaces using ethanol because of weak adhesion and nondestructively transferred to various substrates taking advantage of the capillarity. Furthermore, sensitive light‐driven McPCPF locomotion on organic liquid surfaces is demonstrated. Ultimately, a facile strategy for the construction of free‐standing 3D microstructure‐patterned conducting polymer films is proposed, which can improve productivity and applicability of the films in different fields and expand the application scope of superwettable interfaces.