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A novel light-induced shape-memory material based on poly(l-lactide)-poly(ethylene glycol) copolymer is developed successfully by dangling the photoresponsive anthracene group on the PEG soft segment selectively. For synthesis strategy, the preprepared photoresponsive monomer N,N-bis(2-hydroxyethyl)-9-anthracene-methanamine (BHEAA) is first embedded into PEG chains; then, we couple this anthracene-functionalized PEG precursor with PLA precursor to result in PLA-PEG-A copolymer. The composition of target product can be well-defined by simply adjusting the feed ratio. The chemical structures of intermediate and final products are confirmed by (1)H NMR. Differential scanning calorimetry analysis of material reveals that the PEG soft segment became noncrystallizable when 4% or more BHEAA is introduced, and this feature is beneficial to the mobility of anthracene groups in polymer matrix. The static tensile tests show that the samples exhibit rubberlike mechanical properties except for the PLA-dominant one. The reversibility of [4 + 4] cycloaddition reaction between pendant anthracene groups in PLA-PEG-A film is demonstrated by UV-vis. Eventually, the light-induced shape-memory effect (LSME) is successfully realized in PLA-PEG-A. The results of cyclic photomechanical tests also reveal that the content of PLA hard segment as well as photosensitive anthracene moieties plays a crucial role in LSME.

Currently, a variety of elastomers with a self-healing capacity and reprocessability have been developed by dynamic chemistry to extend the service life, increase the reliability of polymeric materials, and reduce the waste. However, it is still a large challenge to seek an appropriate dynamic interaction that may perfectly match the general performance of the target polymeric materials such as polyurethane. Herein, we report a poly-(thiourethane-urethane) (PTUU−N x ) elastomer containing dynamic thiourethane bonds prepared via a thiol−isocyanate click reaction, which is stable at room temperature, healable at moderate temperature, and reprocessable at high temperature. Importantly, it exhibits a mechanical strength similar to the polyurethane because of a very similar structure. The dynamic feature of PTUU−N x is demonstrated theoretically and experimentally to originate from the exchange of thiourethane bonds via the reversible generation of isocyanates and thiols. Most importantly, the thiourethane bond possesses a much lower bond dissociation energy than the urethane bond, which not only makes PTUU−N x elastomers easier to be reprocessed but also endows them with a desirable self-healing ability under moderate conditions. In addition, the optimized sample PTUU−N 2 is utilized to fabricate a conductive device by coating Ag glue on the elastomer surface and inserting the coated elastomer into a circuit, which displays a high self-healing efficiency, as the material recovers to its original mechanical property and conductivity. Therefore, these results not only indicate that the PTUU−N x elastomers have considerable potential for applications in intelligent electronic devices but also provide new ideas for developing new self-healing materials by applying the adaptable dynamic bond to the target polymers.

Lithium tetrafluoroborate (LiBF4) used as an electrolyte additive to improve the cycling performance of LiNi0.5Co0.2Mn0.3O2/graphite cell at higher operating voltage is investigated. With 1.0 wt% LiBF4 addition into the electrolyte, the capacity retention of lithium ion battery after 100 cycles was greatly improved from 29.2% to 90.1% in the voltage of 3.0 V–4.5 V. To understand the mechanism of the capacity retention enhancement at high voltage operation, the properties including the cell performance, the impedance behavior as well as the characteristics of the electrode interfacial properties are examined. It is found that LiBF4 was likely to participate in the formation of interface film on both electrodes. The improved performances of the cell are attributed to the modification of interface layer components on graphite anode and LiNi0.5Co0.2Mn0.3O2 cathode, which leading to lower the interfacial impedance.

Self-healing materials have attracted considerable attention because of their improved safety, lifetime, energy efficiency and environmental impact. Supramolecular interactions have been extensively considered in the field of self-healing materials due to their excellent reversibility and sensitive responsiveness to environmental stimuli. However, development of a polymeric material with good mechanical performance as well as self-healing capacity is very challenging. In this study, we report a robust self-healing polyurethane (PU) elastomer polypropylene glycol-2-amino-5-(2hydroxyethyl)-6-methylpyrimidin-4-ol (PPG-mUPy) by integrating ureidopyrimidone (UPy) motifs with a PPG segment with a well-defined architecture and microphase morphology. To balance the self-healing capacity and mechanical performance, a thermal-triggered switch of H-bonding is introduced. The quadruple H-bonded UPy dimeric moieties in the backbone induce phase separation to form a hard domain as well as enable further aggregation into microcrystals by virtue of the stacking interactions, which are stable in ambient temperature. This feature endows the PU with high mechanical strength. Meanwhile, a high healing efficiency can be realized, when the reversibility of the H-bond was unlocked from the stacking at higher temperature. An optimized sample PPG 1000-mUPy 50% with a good balance of mechanical performance (20.62 MPa of tensile strength) and healing efficiency (93% in tensile strength) was achieved. This strategy will provide a new idea for developing robust self-healing polymers.

Two-way shape-memory polymers (2W-SMPs) show great potential in actuating applications such as robotics due to their reversibility; indeed, multiresponsive 2W-SMPs are more expected. Inspired by the fascinating adhesion effects of mussels, we herein describe a metallo-supramolecular poly­(ε-caprolactone) (PCL)-based network constructed around catechol chemistry, leading to excellent thermal/magnetic/light-responsive two-way shape-memory effects (2W-SME) as well as self-healing capacity. These hybrid networks get readily self-assembled upon metal coordination interaction between superparamagnetic iron oxide nanoparticles (Fe3O4 NPs) and catechol-telechelic PCL. The incorporation of Fe3O4 NPs may act as the strong netpoints which allow the networks with excellent thermal-responsive one-way (1W) and 2W-SME, due to the ability of the semicrystalline PCL segments to present both crystallization-induced elongation (CIE) and melting-induced contraction (MIC) under constant stress. As a multifunctional medium, moreover, it also endows the hybrids with the magnetic-responsive 2W-SME in an alternating magnetic field and the light-induced SME triggered by the near-infrared light. Thanks to the dynamic nature of this metal coordination interaction inspired by mussel, the target hybrid networks also showed good self-healing capability. A model of magnetic-triggered actuator was well-established, which allows to the material with interesting applications such as remote-control or intelligent magnetic-sensitive devices.

Covalently cross-linked network has been widely applied in triple-shape memory polymers (TSPs), and fabricating triple-shape memory networks with the optional shapes through a facile and fast way is highly expected in the real applications. In this study, a "preshaped and post-cross-linking" strategy has been put forward to fabricate the triple-shape networks via fast photo-cross-linking in solid state. The photoresponsive anthracene group was first employed to develop a poly(D,L-lactide)−poly(tetramethylene oxide) glycol (PDLLA-PTMEG) network via UV light irradiation. Two steps were involved in network fabrication: first, linear copolymers (AN-PDLLA-PTMEG) containing anthracene groups on the side chains with different mass ratio of PDLLA segments were synthesized, and then PDLLA-PTMEG networks (NW-PDLLA-PTMEG) were formed by 365 nm UV light irradiation under an argon atmosphere. The structures of all the precursors were determined by 1 H NMR, and all networks were evaluated by swelling tests. The results of tensile tests show that the content of PDLLA segments has a crucial effect on the mechanical performance of the materials. Differential scanning calorimetry (DSC) analysis combined with dynamic mechanical analysis (DMA) reveals that all the NW-PDLLA-PTMEG's display two thermal transitions (T m,PTMEG and T g,PDLLA ), which can be utilized as T trans to trigger triple-shape memory behavior. The cyclic thermal mechanical testing for triple-shape effects of NW-PDLLA-PTMEG, which was performed by DMA, demonstrates that the mass ratio of two segments has a great effect on the shape fixity and shape recovery. Moreover, a practical application as heat-shrinkable tube (or film) has been put forward.