Highly Recyclable and Tough Elastic Vitrimers from a Defined Polydimethylsiloxane Network

Author:

Luo Jiancheng1,Zhao Xiao1,Ju Hao2,Chen Xiangjun3,Zhao Sheng4,Demchuk Zoriana1,Li Bingrui5,Bocharova Vera1,Carrillo Jan‐Michael Y.6ORCID,Keum Jong K.67ORCID,Xu Sheng3,Sokolov Alexei P.14,Chen Jiayao2ORCID,Cao Peng‐Fei2ORCID

Affiliation:

1. Chemical Sciences Division Oak Ridge National Laboratory Oak Ridge TN-37830 USA

2. State Key Laboratory of Organic-Inorganic Composites Beijing University of Chemical Technology Beijing 100029 China

3. Materials Science and Engineering Program University of California San Diego La Jolla CA-92093 USA

4. Department of Chemistry University of Tennessee Knoxville TN-37996 USA

5. The Bredesen Center for Interdisciplinary Research and Graduate Education University of Tennessee Knoxville TN-37996 USA

6. Center for Materials Sciences Oak Ridge National Laboratory Oak Ridge TN-37830 USA

7. Neutron Scattering Division Oak Ridge National Laboratory Oak Ridge TN-37830 USA

Abstract

AbstractDespite intensive research on sustainable elastomers, achieving elastic vitrimers with significantly improved mechanical properties and recyclability remains a scientific challenge. Herein, inspired by the classical elasticity theory, we present a design principle for ultra‐tough and highly recyclable elastic vitrimers with a defined network constructed by chemically crosslinking the pre‐synthesized disulfide‐containing polydimethylsiloxane (PDMS) chains with tetra‐arm polyethylene glycol (PEG). The defined network is achieved by the reduced dangling short chains and the relatively uniform molecular weight of network strands. Such elastic vitrimers with the defined network, i.e., PDMS‐disulfide‐D, exhibit significantly improved mechanical performance than random analogous, previously reported PDMS vitrimers, and even commercial silicone‐based thermosets. Moreover, unlike the vitrimers with random network that show obvious loss in mechanical properties after recycling, those with the defined network enable excellent thermal recyclability. The PDMS‐disulfide‐D also deliver comparable electrochemical signals if utilized as substrates for electromyography sensors after the recycling. The multiple relaxation processes are revealed via a unique physical approach. Multiple techniques are also applied to unravel the microscopic mechanism of the excellent mechanical performance and recyclability of such defined network.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for Central Universities of the Central South University

Fundamental Research Funds for the Central Universities

Air Force Research Laboratory

Publisher

Wiley

Subject

General Chemistry,Catalysis

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