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Sequentially photocatalytic degradation of mussel-inspired polydopamine: From nanoscale disassembly to effective mineralization.

Authors :
Liu, Xinghuan
Li, Danya
Tabassum, Mehwish
Huang, Chao
Yi, Ke
Fang, Tianwen
Jia, Xin
Source :
Journal of Colloid & Interface Science. Oct2024, Vol. 672, p329-337. 9p.
Publication Year :
2024

Abstract

The photodegradation and deadhesion of mussel-inspired polydopamine was reported from nanoscale disassembly to effective mineralization. Various PDA coated templates and PDA hollow structures can be photodegraded by this strategy. The patterned and gradient surfaces were prepared by the "top-down" method under the control of light scope and intensity, respectively. [Display omitted] Mussel-inspired polydopamine (PDA) coating has been utilized extensively as versatile deposition strategies that can functionalize surfaces of virtually all substrates. However, the strong adhesion, stability and intermolecular interaction of PDA make it inefficient in certain applications. Herein, a green and efficient photocatalytic method was reported to remove adhesion and degrade PDA by using TiO 2 -H 2 O 2 as photocatalyst. The photodegradation process of the PDA spheres was first undergone nanoscale disassembly to form soluble PDA oligomers or well-dispersed nanoparticles. Most of the disassembled PDA can be photodegraded and finally mineralized to CO 2 and H 2 O. Various PDA coated templates and PDA hollow structures can be photodegraded by this strategy. Such process provides a practical strategy for constructing the patterned and gradient surfaces by the "top-down" method under the control of light scope and intensity. This sequential degradation strategy is beneficial to achieve the decomposition of highly crosslinked polymers. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
672
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
178233476
Full Text :
https://doi.org/10.1016/j.jcis.2024.06.008