Search

We developed a procedure for the reliable and reproducibleformation of monodispersed polymer nanocrystals whose morphologiescan be easily controlled to produce structures ranging from nanoparticlesto nanorods. The directional cooling crystallization of ferroelectricpolymer solutions under nanoconfinement allowed polyvinylidene fluorideto form single crystalline monodisperse nanocrystals without the useof surfactants or stabilizers. An important growth condition necessaryto yield highly crystalline ferroelectric polymers was a regulatedthermal gradient under nanoconfinement to induce uniform nucleationand controlled directional growth. While other methods involving thenanoconfined crystallization of polymers are restricted to yield nanofibersor nanotubes with a high aspect ratio, our unidirectional coolingmethod produced nanocrystals of ferroelectric polymers with nanosphere,nanocapsule, and nanorod structures. Field-emission scanning electronmicroscopy, transmission electron microscopy, dynamic contact electrostaticforce microscopy, grazing incidence X-ray diffraction, and differentialscanning calorimetry were used to characterize the morphologies andstructures of the nanocrystals. The results suggest that the directionalcooling method facilitates nucleation and directional growth by controllingdiffusion and promoting molecular alignment from the preferred crystalorientations due to the unidirectional thermal gradient. This studyprovides a novel method of rational material design to fabricate polymernanocrystals by directing nucleation and growth of molecular crystalsfrom solution. [ABSTRACT FROM AUTHOR]

Stretchable energy storage devices are of great interest because of their potential applications in body-friendly, skin-like, wearable devices. However, stretchable batteries are very challenging to fabricate. The electrodes must have a degree of stretchability because the active materials occupy most of the volume, and the separator and packaging should also be stretchable. Here, an all-component stretchable lithium-ion battery was realized by leveraging the structural stretchability of re-entrant micro-honeycomb graphene-carbon nanotube (CNT)/active material composite electrodes and a physically cross-linked gel electrolyte, without using an inactive elastomeric substrate or matrix. Active materials interconnected via the entangled CNT and graphene sheets provided a mechanically stable porous network framework, and the inwardly protruding framework in the re-entrant honeycomb structure allowed for structural stretching during deformation. The composite network consisting solely of binder-free, highly conductive materials provided superior electron transfer, and vertically aligned microchannels enabled facile ion transport. Additionally, the physically cross-linked gel electrolyte increased the mechanical stability upon deformation of the electrodes and was effective as a stretchable separator. The resulting stretchable battery showed a high areal capacity of 5.05 mAh·cm -2 , superior electrochemical performance up to 50% strain under repeated (up to 500) stretch-release cycles, and long-term stability of 95.7% after 100 cycles in air conditions.

Superparamagnetic iron oxide nanoparticles (SPIONs) are often encapsulated into drug-carrying nano/microsized particles for simultaneous magnetic resonance (MR) imaging and treatment of diseased tissues. Unfortunately, encapsulated SPIONs may have a limited ability to modulate the T 2 -weighted relaxation of water protons, but this insight has not been examined systematically. This study demonstrates that SPIONs immobilized on 200 nm diameter poly(lactic- co-glycolic acid) (PLGA) nanoparticles using Pickering emulsification present 18-fold higher relaxivity than encapsulated SPIONs and 1.5-fold higher relaxivity than free SPIONs. In contrast, the SPIONs immobilized on 10 μm diameter PLGA particles exhibit a minor increase in MR relaxivity. This interesting finding will significantly impact current efforts to synthesize and assemble advanced MR contrast agents.

Overproduced reactive oxygen species (ROS) are closely related to various health problems including inflammation, infection, and cancer. Abnormally high ROS levels can cause serious oxidative damage to biomolecules, cells, and tissues. A series of nano- or microsized particles has been developed to reduce the oxidative stress level by delivering antioxidant drugs. However, most systems are often plagued by slow molecular discharge, driven by diffusion. Herein, this study demonstrates the polymeric particles whose internal pressure can increase upon exposure to H 2 O 2 , one of the ROS, and in turn, discharge antioxidants actively. The on-demand pressurized particles are assembled by simultaneously encapsulating water-dispersible manganese oxide (MnO 2 ) nanosheets and green tea derived epigallocatechin gallate (EGCG) molecules into a poly(lactic-co-glycolic acid) (PLGA) spherical shell. In the presence of H 2 O 2 , the MnO 2 nanosheets in the PLGA particle generate oxygen gas by decomposing H 2 O 2 and increase the internal pressure. The pressurized PLGA particles release antioxidative EGCG actively and, in turn, protect vascular and brain tissues from oxidative damage more effectively than the particles without MnO 2 nanosheets. This H 2 O 2 responsive, self-pressurizing particle system would be useful to deliver a wide array of molecular cargos in response to the oxidation level.

Hydrogels in nature seldom form a single phase, more often forming structured phases with other soft phases, allowing nature to develop responsive and adaptive strategies. Based on knowledge of how hydrogels are utilized in nature, we developed novel 3D cocontinuous composites from soft materials with extremely different properties, a hydrogel and a silicone. These were successfully prepared by infiltrating liquid polydimethylsiloxane (PDMS) into poly( N -isopropylacrylamide) (PNIPAm) frameworks of aligned pores prepared by directional melt crystallization. The composites had outstanding modulus and swelling ratio compared to other mechanically strong hydrogels. More interestingly, the deswelling kinetics were dramatically accelerated (by a factor of 1000), possibly due to the aligned microchannels and the hydrophobic nature of PDMS. As a result, an actuator movement mimicking flowering could be completed in less than 20 s. This novel and versatile cocontinuous composite strategy could overcome the current limitations of soft materials.

Networks of silver nanowires (Ag NWs) have been considered as promising materials for stretchable and transparent conductors. Despite various improvements of their optoelectronic and electromechanical properties over the past few years, Ag NW networks with a sufficient stretchability in multiple directions that is essential for the accommodation of the multidirectional strains of human movement have seldom been reported. For this paper, biaxially stretchable, transparent conductors were developed based on 2D mass-spring networks of wavy Ag NWs. Inspired by the traditional papermaking process, the 2D wavy networks were produced by floating Ag NW networks on the surface of water and subsequently applying biaxial compression to them. It was demonstrated that this floating-compression process can reduce the friction between the Ag NW-water interfaces, providing a uniform and isotropic in-plane waviness for the networks without buckling or cracking. The resulting Ag NW networks that were transferred onto elastomeric substrates successfully acted as conductors with an excellent transparency, conductivity, and electromechanical stability under a biaxial strain of 30%. The strain sensors that are based on the prepared conductors demonstrated a great potential for the enhanced performances of future wearable devices.

We report a facile approach for producing reversibly stretchable, optically transparent radio-frequency antennas based on wavy Ag nanowire (NW) networks. The wavy configuration of Ag NWs is obtained by floating the NW networks on the surface of water, followed by compression. Stretchable antennas are prepared by transferring the compressed NW networks onto elastomeric substrates. The resulting antennas show excellent performance under mechanical deformation due to the wavy configuration, which allows the release of stress applied to the NWs and an increase in the contact area between NWs. The antennas formed from the wavy NW networks exhibit a smaller return loss and a higher radiation efficiency when strained than the antennas formed from the straight NW networks, as well as an improved stability in cyclic deformation tests. Moreover, the wavy NW antennas require a relatively small quantity of NWs, which leads to low production costs and provides an optical transparency. These results demonstrate the potential of these wavy Ag NW antennas in applications of wireless communications for wearable systems.