| Literature DB >> 28640515 |
Cheng Zhu1, Yijun Fu1, Changan Liu1, Yang Liu1, Lulu Hu1, Juan Liu1, Igor Bello1, Hao Li1, Naiyun Liu1, Sijie Guo1, Hui Huang1, Yeshayahu Lifshitz1,2, Shuit-Tong Lee1, Zhenhui Kang1.
Abstract
Self-healing is the way by which nature repairs damage and prolongs the life of bio entities. A variety of practical applications require self-healing materials in general and self-healing polymers in particular. Different (complex) methods provide the rebonding of broken bonds, suppressing crack, or local damage propagation. Here, a simple, versatile, and cost-effective methodology is reported for initiating healing in bulk polymers and self-healing and anticorrosion properties in polymer coatings: introduction of carbon dots (CDs), 5 nm sized carbon nanocrystallites, into the polymer matrix forming a composite. The CDs are blended into polymethacrylate, polyurethane, and other common polymers. The healing/self-healing process is initiated by interfacial bonding (covalent, hydrogen, and van der Waals bonding) between the CDs and the polymer matrix and can be optimized by modifying the functional groups which terminate the CDs. The healing properties of the bulk polymer-CD composites are evaluated by comparing the tensile strength of pristine (bulk and coatings) composites to those of fractured composites that are healed and by following the self-healing of scratches intentionally introduced to polymer-CD composite coatings. The composite coatings not only possess self-healing properties but also have superior anticorrosion properties compared to those of the pure polymer coatings.Entities:
Keywords: carbon dots; corrosion resistance properties; healing/self-healing; interfacial bonding; polymers
Year: 2017 PMID: 28640515 DOI: 10.1002/adma.201701399
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849