Highly Stretchable, Fast Self-Healing, and Waterproof Fluorinated Copolymer Ionogels with Selectively Enriched Ionic Liquids for Human-Motion Detection

The development of waterproof ionogels with high stretchability and fast self-healing performance is essential for stretchable ionic conductors in sophisticated skin-inspired wearable sensors but can be rarely met in one material. Herein, a semicrystalline fluorinated copolymer ionogel (SFCI) with extremely high stretchability, underwater stability, and fast self-healability was fabricated, among which hydrophobic ionic liquids ([BMIM]­[TFSI]) were selectively enriched in fluoroacrylate segment domains of the fluorinated copolymer matrix through unique ion–dipole interactions. Benefiting from the reversible ion–dipole interactions between the [BMIM]­[TFSI] and fluoroacrylate segment domains as well as the physical cross-linking effects of semicrystalline oligoethylene glycol domains, the SFCI exhibited ultrastretchability (>6000%), fast room-temperature self-healability (>96% healing efficiency after cutting and self-healing for 30 min), and outstanding elasticity. In addition, the representative SFCI also exhibited high-temperature tolerance up to 300 °C, antifreezing performance as low as −35 °C, and high transparency (>93% visible-light transmittance). As a result, the as-obtained SFCI can readily be used as a highly stretchable ionic conductor in skin-inspired wearable sensors with waterproof performance for real-time detecting physiological human activities. These attractive features illustrate that the developed ultrastretchable and rapidly self-healable ionogels with unique waterproofness are promising candidates especially for sophisticated wearable strain sensing applications in complex and extreme environments

Highly Stretchable, Fast Self-Healing, and Waterproof Fluorinated Copolymer Ionogels with Selectively Enriched Ionic Liquids for Human-Motion Detection

The development of waterproof ionogels with high stretchability and fast self-healing performance is essential for stretchable ionic conductors in sophisticated skin-inspired wearable sensors but can be rarely met in one material. Herein, a semicrystalline fluorinated copolymer ionogel (SFCI) with extremely high stretchability, underwater stability, and fast self-healability was fabricated, among which hydrophobic ionic liquids ([BMIM]­[TFSI]) were selectively enriched in fluoroacrylate segment domains of the fluorinated copolymer matrix through unique ion–dipole interactions. Benefiting from the reversible ion–dipole interactions between the [BMIM]­[TFSI] and fluoroacrylate segment domains as well as the physical cross-linking effects of semicrystalline oligoethylene glycol domains, the SFCI exhibited ultrastretchability (>6000%), fast room-temperature self-healability (>96% healing efficiency after cutting and self-healing for 30 min), and outstanding elasticity. In addition, the representative SFCI also exhibited high-temperature tolerance up to 300 °C, antifreezing performance as low as −35 °C, and high transparency (>93% visible-light transmittance). As a result, the as-obtained SFCI can readily be used as a highly stretchable ionic conductor in skin-inspired wearable sensors with waterproof performance for real-time detecting physiological human activities. These attractive features illustrate that the developed ultrastretchable and rapidly self-healable ionogels with unique waterproofness are promising candidates especially for sophisticated wearable strain sensing applications in complex and extreme environments

Highly Stretchable, Fast Self-Healing, and Waterproof Fluorinated Copolymer Ionogels with Selectively Enriched Ionic Liquids for Human-Motion Detection

The development of waterproof ionogels with high stretchability and fast self-healing performance is essential for stretchable ionic conductors in sophisticated skin-inspired wearable sensors but can be rarely met in one material. Herein, a semicrystalline fluorinated copolymer ionogel (SFCI) with extremely high stretchability, underwater stability, and fast self-healability was fabricated, among which hydrophobic ionic liquids ([BMIM]­[TFSI]) were selectively enriched in fluoroacrylate segment domains of the fluorinated copolymer matrix through unique ion–dipole interactions. Benefiting from the reversible ion–dipole interactions between the [BMIM]­[TFSI] and fluoroacrylate segment domains as well as the physical cross-linking effects of semicrystalline oligoethylene glycol domains, the SFCI exhibited ultrastretchability (>6000%), fast room-temperature self-healability (>96% healing efficiency after cutting and self-healing for 30 min), and outstanding elasticity. In addition, the representative SFCI also exhibited high-temperature tolerance up to 300 °C, antifreezing performance as low as −35 °C, and high transparency (>93% visible-light transmittance). As a result, the as-obtained SFCI can readily be used as a highly stretchable ionic conductor in skin-inspired wearable sensors with waterproof performance for real-time detecting physiological human activities. These attractive features illustrate that the developed ultrastretchable and rapidly self-healable ionogels with unique waterproofness are promising candidates especially for sophisticated wearable strain sensing applications in complex and extreme environments

Highly Stretchable, Fast Self-Healing, and Waterproof Fluorinated Copolymer Ionogels with Selectively Enriched Ionic Liquids for Human-Motion Detection

The development of waterproof ionogels with high stretchability and fast self-healing performance is essential for stretchable ionic conductors in sophisticated skin-inspired wearable sensors but can be rarely met in one material. Herein, a semicrystalline fluorinated copolymer ionogel (SFCI) with extremely high stretchability, underwater stability, and fast self-healability was fabricated, among which hydrophobic ionic liquids ([BMIM]­[TFSI]) were selectively enriched in fluoroacrylate segment domains of the fluorinated copolymer matrix through unique ion–dipole interactions. Benefiting from the reversible ion–dipole interactions between the [BMIM]­[TFSI] and fluoroacrylate segment domains as well as the physical cross-linking effects of semicrystalline oligoethylene glycol domains, the SFCI exhibited ultrastretchability (>6000%), fast room-temperature self-healability (>96% healing efficiency after cutting and self-healing for 30 min), and outstanding elasticity. In addition, the representative SFCI also exhibited high-temperature tolerance up to 300 °C, antifreezing performance as low as −35 °C, and high transparency (>93% visible-light transmittance). As a result, the as-obtained SFCI can readily be used as a highly stretchable ionic conductor in skin-inspired wearable sensors with waterproof performance for real-time detecting physiological human activities. These attractive features illustrate that the developed ultrastretchable and rapidly self-healable ionogels with unique waterproofness are promising candidates especially for sophisticated wearable strain sensing applications in complex and extreme environments

Graphene-Wrapped Polyaniline Hollow Spheres As Novel Hybrid Electrode Materials for Supercapacitor Applications

Polyaniline hollow spheres (PANI-HS)@electrochemical reduced graphene oxide (ERGO) hybrids with core–shell structures have been fabricated <i>via</i> a solution-based coassembly process. The hollow nanostructured designing for the PANI-HS greatly enlarges the specific surface area, providing high electroactive regions and short diffusion lengths for both charge and ion transport. The wrapping of ERGO sheets on the PANI-HS can offer highly conductive pathways by bridging individual PANI-HS together, thus facilitating the rate and cycling performance of supercapacitors. The specific capacitance of PANI-HS36@ERGO hybrids can reach 614 F g^–1 at a current density of 1 A g^–1. Furthermore, the capacitance of the PANI-HS36@ERGO hybrids maintains 90% after 500 charging/discharging cycles at a current density of 1 A g^–1, indicating a good cycling stability. The greatly enhanced electrochemical performance can be ascribed to the synergic effects of the two components of PANI-HS and ERGO, suggesting that the PANI-HS@ERGO hybrids as novel electrode materials may have potential applications in high-performance energy storage devices

Bimetallic Platonic Janus Nanocrystals

We demonstrate the creation of Ag-based bimetallic platonic Janus nanostructures by confining galvanic replacement reaction at a nanoscale interface on highly symmetrical nanostructures such as Ag nanocubes and nanooctahedra using reactive microcontact printing (μCP). The extent of galvanic replacement reaction can be controlled kinetically to derive Janus nanostructures with Au nanodots deposited on either one or multiple facets of Ag nanocubes. The selective deposition of Au dots on a single facet of Ag nanocubes breaks the cubic symmetry and brings about unique and anisotropic plasmonic responses. High-resolution cathodoluminescence hyperspectral imaging of single Janus nanocube demonstrates that surface plasmon resonances corresponding to Au and Ag can be excited at different spots on one Janus nanocube. In addition, we demonstrate the fabrication of alternating Janus/non-Janus segments on 2D Ag nanowires by using a line-patterned polydimethylsiloxane (PDMS) stamp for galvanic replacement. Aside from Au, Pt and Pd can also be selectively deposited onto Ag nanocubes. These Janus nanostructures may find important applications in the field of plasmon-enhanced catalysis

Immobilization of Co–Al Layered Double Hydroxides on Graphene Oxide Nanosheets: Growth Mechanism and Supercapacitor Studies

Layered double hydroxides (LDHs) are generally expressed as [M²⁺_1–<i>x</i>M³⁺_<i>x</i> (OH)₂] [A^<i>n</i>–_{<i>x</i>/<i>n</i>}·<i>m</i>H₂O], where M²⁺ and M³⁺ are divalent and trivalent metal cations respectively, and A is <i>n</i>-valent interlayer guest anion. Co–Al layered double hydroxides (LDHs) with different sizes have been grown on graphene oxide (GO) via in situ hydrothermal crystallization. In the synthesis procedure, the GO is partially reduced in company with the formation of Co–Al LDHs. The morphology and structure of LDHs/GO hybrids are characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The growth mechanism of LDHs on GO nanosheets is discussed. Moreover, both LDHs and LDHs/graphene nanosheets (GNS) hybrids are further used as electrochemical supercapacitor materials and their performance is evaluated by cyclic voltammetry (CV) and galvanostatic charge/discharge measurements. It is shown that the specific capacitances of LDHs are significantly enhanced by the hybridization with GNS

Nitrogen-Doped Graphene Nanoribbons as Efficient Metal-Free Electrocatalysts for Oxygen Reduction

Nitrogen-doped graphene nanoribbon (N-GNR) nanomaterials with different nitrogen contents have been facilely prepared via high temperature pyrolysis of graphene nanoribbons (GNR)/polyaniline (PANI) composites. Here, the GNRs with excellent surface integration were prepared by longitudinally unzipping the multiwalled carbon nanotubes. With a high length-to-width ratio, the GNR sheets are prone to form a conductive network by connecting end-to-end to facilitate the transfer of electrons. Different amounts of PANI acting as a N source were deposited on the surface of GNRs via a layer-by-layer approach, resulting in the formation of N-GNR nanomaterials with different N contents after being pyrolyzed. Electrochemical characterizations reveal that the obtained N_8.3-GNR nanomaterial has excellent catalytic activity toward an oxygen reduction reaction (ORR) in an alkaline electrolyte, including large kinetic-limiting current density and long-term stability as well as a desirable four-electron pathway for the formation of water. These superior properties make the N-GNR nanomaterials a promising kind of cathode catalyst for alkaline fuel cell applications

Ultrathin Polypyrrole Layers Boosting MoO₃ as Both Cathode and Anode Materials for a 2.0 V High-Voltage Aqueous Supercapacitor

An aqueous supercapacitor is an emerging energy storage unit on account of its low cost, fast energy delivery rate, and long service life. The energy density of an aqueous supercapacitor can be enlarged via extending the voltage window of electrode materials, while the aqueous electrolyte remains thermodynamically constant at 1.23 V. Herein, an aqueous supercapacitor with a 2.0 V high-voltage window is realized by core–shell MoO3–x/polypyrrole (MP) nanocomposites as both cathode and anode materials. The ultrathin PPy layer on the MoO3 core not only improves the conductivity and cycle stability of the nanocomposites but also acts as a reductant, leading to the formation of oxygen vacancies in the MoO3 core. When used as a cathode material, the potential range of the as-obtained MP nanocomposite is up to 1.0 V. As an anode material, the stable potential range could reach −1.0 V. Due to the large potential range of the cathode and anode, the as-obtained 2.0 V aqueous supercapacitor shows a remarkably high delivery energy of 58.5 Wh kg–1. The synthesis of MP nanocomposites is simple and the electrode performance is significantly enhanced; thus, it is a suitable candidate for high-energy-density aqueous supercapacitors

Ni-Doped Graphene/Carbon Cryogels and Their Applications As Versatile Sorbents for Water Purification

Ni-doped graphene/carbon cryogels (NGCC) have been prepared by adding resorcinol and formaldehyde to suspension of graphene oxide (GO), using Ni²⁺ ions as catalysts for the gelation process to substitute the usually used alkaline carbonates. The metal ions of Ni²⁺ have elevated the cross-linking between GO and RF skeletons, thus strengthening the whole cryogel. The as-formed three-dimensional (3D) interconnected structures, which can be well-maintained after freeze-drying of the hydrogel precursor and subsequent carbonization under an inert atmosphere, exhibit good mechanical properties. During the carbonization process, Ni²⁺ ions are converted into Ni nanoparticles and thus embedded in the interconnected structures. The unique porosity within the interconnected structures endows the cryogels with good capability for the extraction of oils and some organic solvents while the bulk form enables its recycling use. When ground into powders, they can be used as adsorbents for dyestuffs. Therefore, the as-obtained cryogels may find potential applications as versatile candidates for the removal of pollutants from water