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Showing papers on "Composite number published in 2016"


Journal ArticleDOI
TL;DR: A stable lithium–scaffold composite electrode is developed by lithium melt infusion into a 3D porous carbon matrix with “lithiophilic” coating, which possesses a high conductive surface area and excellent structural stability upon galvanostatic cycling.
Abstract: Lithium metal-based battery is considered one of the best energy storage systems due to its high theoretical capacity and lowest anode potential of all. However, dendritic growth and virtually relative infinity volume change during long-term cycling often lead to severe safety hazards and catastrophic failure. Here, a stable lithium–scaffold composite electrode is developed by lithium melt infusion into a 3D porous carbon matrix with “lithiophilic” coating. Lithium is uniformly entrapped on the matrix surface and in the 3D structure. The resulting composite electrode possesses a high conductive surface area and excellent structural stability upon galvanostatic cycling. We showed stable cycling of this composite electrode with small Li plating/stripping overpotential (

717 citations


Journal ArticleDOI
TL;DR: A simple and versatile in situ fabrication of MAPbX3 nanocrystal-embedded polymer composite films is developed by controlling the crystallization process from precursor solutions, exhibiting enhanced photoluminescence properties, improved stability, and excellent piezoelectric and mechanical properties.
Abstract: A simple and versatile in situ fabrication of MAPbX3 nanocrystal-embedded polymer composite films is developed by controlling the crystallization process from precursor solutions. The composite films exhibit enhanced photoluminescence properties, improved stability, and excellent piezoelectric and mechanical properties. Applications of these composite films as color converters in liquid-crystal-display backlights are demonstrated, showing bright potential in display technology.

587 citations


Journal Article
01 Aug 2016-Nature
TL;DR: A new 4D printing approach that can create high resolution (up to a few microns), multimaterial shape memory polymer (SMP) architectures based on high resolution projection microstereolithography (PμSL) and uses a family of photo-curable methacrylate based copolymer networks.
Abstract: We present a new 4D printing approach that can create high resolution (up to a few microns), multimaterial shape memory polymer (SMP) architectures The approach is based on high resolution projection microstereolithography (PμSL) and uses a family of photo-curable methacrylate based copolymer networks We designed the constituents and compositions to exhibit desired thermomechanical behavior (including rubbery modulus, glass transition temperature and failure strain which is more than 300% and larger than any existing printable materials) to enable controlled shape memory behavior We used a high resolution, high contrast digital micro display to ensure high resolution of photo-curing methacrylate based SMPs that requires higher exposure energy than more common acrylate based polymers An automated material exchange process enables the manufacture of 3D composite architectures from multiple photo-curable SMPs In order to understand the behavior of the 3D composite microarchitectures, we carry out high fidelity computational simulations of their complex nonlinear, time-dependent behavior and study important design considerations including local deformation, shape fixity and free recovery rate Simulations are in good agreement with experiments for a series of single and multimaterial components and can be used to facilitate the design of SMP 3D structures

557 citations


Journal ArticleDOI
TL;DR: The excellent absorbing performance together with lightweight and ultrathin thickness endows the CNTs/Co composite with the potential for application in the electromagnetic wave absorbing field.
Abstract: Porous carbon nanotubes/cobalt nanoparticles (CNTs/Co) composite with dodecahedron morphology was synthesized by in situ pyrolysis of the Co-based zeolitic imidazolate framework in a reducing atmosphere. The morphology and microstructure of the composite can be well tuned by controlling the pyrolysis conditions. At lower pyrolysis temperature, the CNTs/Co composite is composed of well-dispersed Co nanoparticles and short CNT clusters with low graphitic degree. The increase of pyrolysis temperature/time promotes the growth and graphitization of CNTs and leads to the aggregation of Co nanoparticles. The optimized CNTs/Co composite exhibits strong dielectric and magnetic losses as well as a good impedance matching property. Interestingly, the CNTs/Co composite displays extremely strong electromagnetic wave absorption with a maximum reflection loss of −60.4 dB. More importantly, the matching thickness of the absorber is as thin as 1.81 mm, and the filler loading of composite in the matrix is only 20 wt %. The...

402 citations


Journal ArticleDOI
TL;DR: The hollow Fe3O4-Fe nanoparticles with average diameter and shell thickness of 20 and 8 nm, respectively, were uniformly anchored on the graphene sheets without obvious aggregation and the minimal reflection loss RL values of the composite could reach -30 dB at the absorber thickness ranging from 2.0 to 5.0 mm.
Abstract: We developed a strategy for coupling hollow Fe3O4–Fe nanoparticles with graphene sheets for high-performance electromagnetic wave absorbing material. The hollow Fe3O4–Fe nanoparticles with average diameter and shell thickness of 20 and 8 nm, respectively, were uniformly anchored on the graphene sheets without obvious aggregation. The minimal reflection loss RL values of the composite could reach −30 dB at the absorber thickness ranging from 2.0 to 5.0 mm, greatly superior to the solid Fe3O4–Fe/G composite and most magnetic EM wave absorbing materials recently reported. Moreover, the addition amount of the composite into paraffin matrix was only 18 wt %.

400 citations


Journal ArticleDOI
TL;DR: The first experimental evidence is provided to show that Li ions favor the pathway through the LLZO ceramic phase instead of the PEO-LLZO interface or PEO.
Abstract: Polymer-ceramic composite electrolytes are emerging as a promising solution to deliver high ionic conductivity, optimal mechanical properties, and good safety for developing high-performance all-solid-state rechargeable batteries. Composite electrolytes have been prepared with cubic-phase Li7 La3 Zr2 O12 (LLZO) garnet and polyethylene oxide (PEO) and employed in symmetric lithium battery cells. By combining selective isotope labeling and high-resolution solid-state Li NMR, we are able to track Li ion pathways within LLZO-PEO composite electrolytes by monitoring the replacement of (7) Li in the composite electrolyte by (6) Li from the (6) Li metal electrodes during battery cycling. We have provided the first experimental evidence to show that Li ions favor the pathway through the LLZO ceramic phase instead of the PEO-LLZO interface or PEO. This approach can be widely applied to study ion pathways in ionic conductors and to provide useful insights for developing composite materials for energy storage and harvesting.

383 citations


Journal ArticleDOI
01 Mar 2016-Carbon
TL;DR: In this article, a phase change composites is prepared by vacuum assisted impregnating of polyethylene glycol (PEG) into the cellulose/GNP aerogels, which exhibit high thermal conductivity, good shape stability and high latent heat of fusion.

357 citations


Journal ArticleDOI
TL;DR: Electrochemical behaviour of a Sn-based anode in a potassium cell is reported for the first time, and Experimental evidence shows that Sn is capable of alloying/de-alloying with potassium in a reversible manner.

345 citations


Journal ArticleDOI
TL;DR: Li10GeP2S12 (LGPS) is incorporated into polyethylene oxide (PEO) matrix to fabricate composite solid polymer electrolyte (SPE) membranes.

339 citations


Journal ArticleDOI
TL;DR: The significantly improved electrochemical performance could be attributed to the unique structure that combines a variety of advantages: easy access of electrolyte to the open channel structure, short transport path of ions through carbon toward the red P, and high ionic and electronic conductivity.
Abstract: Red phosphorus (P) have been considered as one of the most promising anode material for both lithium-ion batteries (LIBs) and (NIBs), because of its high theoretical capacity. However, natural insulating property and the large volume expansion of red P during cycling lead to poor cyclability and low rate performance, which prevents its practical application. Here, we significantly improves both lithium storage and sodium storage performance of red P by confining nanosized amorphous red P into the mesoporous carbon matrix (P@CMK-3) using a vaporization-condensation-conversion process. The P@CMK-3 shows a high reversible specific capacity of ∼ 2250 mA h g(-1) based on the mass of red P at 0.25 C (∼ 971 mA h g(-1) based on the composite), excellent rate performance of 1598 and 624 mA h g(-1) based on the mass of red P at 6.1 and 12 C, respectively (562 and 228 mA h g(-1) based on the mass of the composite at 6.1 and 12 C, respectively) and significantly enhanced cycle life of 1150 mA h g(-1) based on the mass of red P at 5 C (500 mA h g(-1) based on the mass of the composite) after 1000 cycles for LIBs. For Na ions, it also displays a reversible capacity of 1020 mA h g(-1) based on the mass of red P (370 mA h g(-1) based on the mass of the composite) after 210 cycles at 5C. The significantly improved electrochemical performance could be attributed to the unique structure that combines a variety of advantages: easy access of electrolyte to the open channel structure, short transport path of ions through carbon toward the red P, and high ionic and electronic conductivity.

336 citations


Journal ArticleDOI
22 Mar 2016-ACS Nano
TL;DR: The body-attachable CDA can be used as a metal-free, all-in-one component for measuring biosignals under daily activity conditions (i.e., underwater, movements) because of its superior conformality and water-repellent characteristic.
Abstract: Here we propose a concept of conductive dry adhesives (CDA) combining a gecko-inspired hierarchical structure and an elastomeric carbon nanocomposite. To complement the poor electrical percolation of 1D carbon nanotube (CNT) networks in an elastomeric matrix at a low filler content (∼1 wt %), a higher dimensional carbon material (i.e., carbon black, nanographite, and graphene nanopowder) is added into the mixture as an aid filler. The co-doped graphene and CNT in the composite show the lowest volume resistance (∼100 ohm·cm) at an optimized filler ratio (1:9, total filler content: 1 wt %) through a synergetic effect in electrical percolation. With an optimized conductive elastomer, gecko-inspired high-aspect-ratio (>3) microstructures over a large area (∼4 in.2) are successfully replicated from intaglio-patterned molds without collapse. The resultant CDA pad shows a high normal adhesion force (∼1.3 N/cm2) even on rough human skin and an excellent cycling property for repeatable use over 30 times without de...

Journal ArticleDOI
TL;DR: In this article, the authors present a new paradigm to fully recycle epoxy-based carbon fiber reinforced polymer (CFRP) composites, where the epoxy matrix can be dissolved as the EG molecules participate in bond exchange reactions (BERs) within the covalent adaptable network (CAN), effectively breaking the long polymer chains into small segments.
Abstract: Both environmental and economic factors have driven the development of recycling routes for the increasing amount of composite waste generated. This paper presents a new paradigm to fully recycle epoxy-based carbon fiber reinforced polymer (CFRP) composites. After immersing the composite in ethylene glycol (EG) and increasing the temperature, the epoxy matrix can be dissolved as the EG molecules participate in bond exchange reactions (BERs) within the covalent adaptable network (CAN), effectively breaking the long polymer chains into small segments. The clean carbon fibers can be then reclaimed with the same dimensions and mechanical properties as those of fresh ones. Both the dissolution rate and the minimum amount of EG required to fully dissolve the CAN are experimentally determined. Further heating the dissolved solution leads to repolymerization of the epoxy matrix, so a new generation of composite can be fabricated by using the recycled fiber and epoxy; in this way a closed-loop near 100% recycling paradigm is realized. In addition, epoxy composites with surface damage are shown to be fully repaired. Both the recycled and the repaired composites exhibit the same level of mechanical properties as fresh materials.

Journal ArticleDOI
TL;DR: In this paper, vertically aligned and interconnected graphene networks are first used as the filler, which is prepared by a controlled three-step procedure: formation of graphene oxide liquid crystals, oriented freeze casting, and high-temperature annealing reduction under Ar. The obtained composite, at an ultralow graphene loading of 0.92 vol %, exhibits a high thermal conductivity (2.13 W m−1 K−1) that is equivalent to a dramatic enhancement of 1231% compared to the pure matrix.
Abstract: Efficient removal of heat via thermal interface materials has become one of the most critical challenges in the development of modern microelectronic devices. However, traditional polymer composites present limited thermal conductivity even when highly loaded with highly thermally conductive fillers due to the lack of efficient heat transfer channels. In this work, vertically aligned and interconnected graphene networks are first used as the filler, which is prepared by a controlled three-step procedure: formation of graphene oxide liquid crystals, oriented freeze casting, and high-temperature annealing reduction under Ar. The obtained composite, at an ultralow graphene loading of 0.92 vol %, exhibits a high thermal conductivity (2.13 W m–1 K–1) that is equivalent to a dramatic enhancement of 1231% compared to the pure matrix. Furthermore, the composite also presents a much reduced coefficient of thermal expansion (∼37.4 ppm K–1) and increased glass transition temperature (135.4 °C). This strategy provide...

Journal ArticleDOI
TL;DR: In this paper, the effect of Carbon Nanotube (CNT) agglomeration on free vibrations of laminated composite doubly-curved shells and panels reinforced by CNTs is investigated.
Abstract: This paper aims at investigating the effect of Carbon Nanotube (CNT) agglomeration on the free vibrations of laminated composite doubly-curved shells and panels reinforced by CNTs. The great performances of doubly-curved structures are joined with the excellent mechanical properties of CNTs. Several laminations schemes and various CNT exponential distributions along the thickness of the structures are considered. Thus, it is evident that the shell dynamic behavior can be affected by many parameters which characterize the reinforcing phase. A widespread parametric study is performed in order to show the natural frequency variation. The general theoretical model for shell structures is based on the so-called Carrera Unified Formulation (CUF) which allows to consider several Higher-order Shear Deformations Theories (HSDTs). In addition, a complete characterization of the mechanical properties of CNTs is presented. The governing equations for the free vibration analysis are solved numerically by means of the well-known Generalized Differential Quadrature (GDQ) method due to its accuracy, stability and reliability features.

Journal ArticleDOI
Jun Cao1, Chen Chen1, Qing Zhao1, Ning Zhang1, Qiongqiong Lu1, Xinyu Wang1, Zhiqiang Niu1, Jun Chen1 
TL;DR: Flexible nanostructured reduced graphene oxide-sulfur (rGO-S) composite films are fabricated by synchronously reducing and assembling GO sheets with S nanoparticles on a metal surface and can serve as the cathodes of flexible Li-S batteries.
Abstract: Flexible nanostructured reduced graphene oxide-sulfur (rGO-S) composite films are fabricated by synchronously reducing and assembling GO sheets with S nanoparticles on a metal surface. The nanostructured architecture in such composite films not only provides effective pathways for electron transport, but also suppresses the diffusion of polysulfides. Furthermore, they can serve as the cathodes of flexible Li-S batteries.

Journal ArticleDOI
TL;DR: An all-soft-matter composite with exceptional electro-elasto properties is demonstrated by embedding liquid-metal inclusions in an elastomer matrix that exhibits a unique combination of high dielectric constant, low stiffness, and large strain limit.
Abstract: An all-soft-matter composite with exceptional electro-elasto properties is demonstrated by embedding liquid-metal inclusions in an elastomer matrix. This material exhibits a unique combination of high dielectric constant, low stiffness, and large strain limit (ca. 600% strain). The elasticity, electrostatics, and electromechanical coupling of the composite are investigated, and strong agreement with predictions from effective medium theory is found.

Journal ArticleDOI
TL;DR: In this article, the authors track Li ion pathways within LLZO-PEO composite electrolytes by monitoring the replacement of 7Li in the composite electrolyte by 6Li from the 6Li metal electrodes during battery cycling.
Abstract: Polymer–ceramic composite electrolytes are emerging as a promising solution to deliver high ionic conductivity, optimal mechanical properties, and good safety for developing high-performance all-solid-state rechargeable batteries. Composite electrolytes have been prepared with cubic-phase Li7La3Zr2O12 (LLZO) garnet and polyethylene oxide (PEO) and employed in symmetric lithium battery cells. By combining selective isotope labeling and high-resolution solid-state Li NMR, we are able to track Li ion pathways within LLZO-PEO composite electrolytes by monitoring the replacement of 7Li in the composite electrolyte by 6Li from the 6Li metal electrodes during battery cycling. We have provided the first experimental evidence to show that Li ions favor the pathway through the LLZO ceramic phase instead of the PEO-LLZO interface or PEO. This approach can be widely applied to study ion pathways in ionic conductors and to provide useful insights for developing composite materials for energy storage and harvesting.

Journal ArticleDOI
TL;DR: In this article, the experimental and theoretical methods to enhance the thermal conductivity of the phase change materials (PCMs) are summarized, and thermal conductivities inserts/additives in recent investigations are listed and summarized.
Abstract: Thermal energy storage systems have been recognized as one of the most efficient ways to enhance the energy efficiency and sustainability, and have received a growing attention in recent years. The use of phase change materials (PCMs) in building applications can not only improve the indoor thermal comfort but also enhance the energy efficiency. The necessity to enhance thermal conductivity of the PCMs is evident due to its low energy charging/discharging rates. Therefore, the high thermal conductivity additives or inserts to enhance thermal conductivity or to form the composite PCM are sought to achieve high energy charging/discharging rates. In this paper, the experimental and theoretical methods to enhance the thermal conductivity of the PCMs are summarized, and the thermal conductivity inserts/additives in recent investigations are listed and summarized. The evaluation of each thermal conductivity enhancement method is discussed.

Journal ArticleDOI
TL;DR: In this article, the authors present an overview of the compatibility between the heterogeneous constituents of plant fibre composite, various modification approaches aiming at overcoming the incompatibility and refining the interfacial adhesion of the composite, interfacial bonding mechanisms, and the assessment of interface structure and bonding.
Abstract: The development of plant fibre composite is on the rise for a wide range of applications. Probably a single most important aspect with respect to the formulation of plant fibre composites with superior mechanical performance is the optimization of the interfacial bonding between the reinforcing plant fibre and polymer matrix. While the interface plays a pivotal role in determining the mechanical properties, e.g. transferring the stress and distributing the bond, it is among the least understood components of the composite. This paper presents an overview of the compatibility between the heterogeneous constituents of plant fibre composite, various modification approaches aiming at overcoming the incompatibility and refining the interfacial adhesion of the composite, interfacial bonding mechanisms, and the assessment of interface structure and bonding. It has been found that 1) the physical and chemical incompatibility between the fibre and matrix, leading to poor dispersion, weak interfacial adhesion and ultimately inferior composite quality, could be overcome through strategical modifications; 2) inter-diffusion, electrostatic adhesion, chemical reactions and mechanical interlocking are in general responsible for the interfacial bonding and adhesion of plant fibre composites; and 3) a thorough knowledge of structure-property relationship of the composite could be established by conducting a set of direct and indirect interfacial assessments. This paper finishes with some critical suggestions and future perspectives, underscoring the roles of composite material researchers and engineers for the further in-depth studies and up-scale commercialization of plant fibre composite.

Journal ArticleDOI
Shuan Liu1, Lin Gu1, Haichao Zhao1, Jianmin Chen1, Haibin Yu1 
TL;DR: Graphene (G) was dispersed uniformly in water and used as an inhibitor in waterborne epoxy coatings and the effect of dispersed G on anticorrosion performance was evaluated.

Patent
16 Sep 2016
TL;DR: In this article, a method and apparatus for the additive manufacturing of three-dimensional objects are described, where two or more materials are extruded simultaneously as a composite, with at least one material in liquid form and at least another material in a solid continuous strand completely encased within the liquid material.
Abstract: A method and apparatus for the additive manufacturing of three-dimensional objects are disclosed. Two or more materials are extruded simultaneously as a composite, with at least one material in liquid form and at least one material in a solid continuous strand completely encased within the liquid material. A means of curing the liquid material after extrusion hardens the composite. A part is constructed using a series of extruded composite paths. The strand material within the composite contains specific chemical, mechanical, or electrical characteristics that instill the object with enhanced capabilities not possible with only one material.

Journal ArticleDOI
TL;DR: A high performance nanostructured anode material for sodium-ion batteries that is fabricated by high energy ball milling to form black phosphorus/Ketjenblack-multiwalled carbon nanotubes (BPC) composite that could deliver a very high initial Coulombic efficiency and high specific capacity.
Abstract: Sodium-ion batteries are promising alternatives to lithium-ion batteries for large-scale applications. However, the low capacity and poor rate capability of existing anodes for sodium-ion batteries are bottlenecks for future developments. Here, we report a high performance nanostructured anode material for sodium-ion batteries that is fabricated by high energy ball milling to form black phosphorus/Ketjenblack–multiwalled carbon nanotubes (BPC) composite. With this strategy, the BPC composite with a high phosphorus content (70 wt %) could deliver a very high initial Coulombic efficiency (>90%) and high specific capacity with excellent cyclability at high rate of charge/discharge (∼1700 mAh g–1 after 100 cycles at 1.3 A g–1 based on the mass of P). In situ electrochemical impedance spectroscopy, synchrotron high energy X-ray diffraction, ex situ small/wide-angle X-ray scattering, high resolution transmission electronic microscopy, and nuclear magnetic resonance were further used to unravel its superior sodi...

Journal ArticleDOI
TL;DR: It is shown that polymeric composites with silver nanoparticle-deposited boron nitride nanosheets as fillers could effectively enhance the thermal conductivity of polymer, thanks to the bridging connections of silver nanoparticles among borons nitride Nanosheet interfaces.
Abstract: Polymer composites with high thermal conductivity have recently attracted much attention, along with the rapid development of the electronic devices toward higher speed and performance. However, a common method to enhance polymer thermal conductivity through an addition of high thermally conductive fillers usually cannot provide an expected value, especially for composites requiring electrical insulation. Here, we show that polymeric composites with silver nanoparticle-deposited boron nitride nanosheets as fillers could effectively enhance the thermal conductivity of polymer, thanks to the bridging connections of silver nanoparticles among boron nitride nanosheets. The thermal conductivity of the composite is significantly increased from 1.63 W/m-K for the composite filled with the silver nanoparticle-deposited boron nitride nanosheets to 3.06 W/m-K at the boron nitride nanosheets loading of 25.1 vol %. In addition, the electrically insulating properties of the composite are well preserved. Fitting the measured thermal conductivity of epoxy composite with one physical model indicates that the composite with silver nanoparticle-deposited boron nitride nanosheets outperforms the one with boron nitride nanosheets, owning to the lower thermal contact resistance among boron nitride nanosheets’ interfaces. The finding sheds new light on enhancement of thermal conductivity of the polymeric composites which concurrently require the electrical insulation.

Journal ArticleDOI
TL;DR: In this article, the AA6351-AlN composites were characterized using scanning electron microscope (SEM) and x-ray diffraction (XRD) and the mechanical properties such as micro-hardness, compression strength, flexural strength and tensile strength of the proposed composite have been studied.
Abstract: In the present investigation, AA6351 aluminum alloy matrix composites reinforced with various percentages of AlN particles were fabricated by stir casting technique. The percentage of AlN was varied from 0 to 20% in a step of 4%. The prepared AA6351-AlN composites were characterized using scanning electron microscope (SEM) and x-ray diffraction (XRD). The mechanical properties such as micro-hardness, compression strength, flexural strength, and tensile strength of the proposed composite have been studied. X-ray diffraction patterns confirm the presence of AlN particles in the composites. SEM analysis reveals the homogeneous distribution of AlN particles in the AA6351 matrix. The mechanical properties of the composite were found to be noticeably higher than that of the plain matrix alloy due to augmented particle content. The produced composites exhibit superior mechanical properties when compared with unreinforced matrix alloy. Fracture surface analysis of tensile specimens show the ductile–brittle nature of failure in the composites.

Journal ArticleDOI
TL;DR: A comprehensive review of the development of multilayer composite membranes for CO 2 separation can be found in this paper, where various composite membrane preparation methods were compared, advances in composite membranes were summarized with detailed data, and challenges facing for the CO2 separation using composite membranes, such as aging, plasticization and long-term stability, were discussed.

Journal ArticleDOI
TL;DR: In this article, a modified Hummers' method was used to prep graphene oxide (GO) sheets with the negative charge and Al powders were coated by hexadecyl trimethyl ammonium bromide (CTAB) to obtain the surface positive charge.

Journal ArticleDOI
TL;DR: In this article, the removal of ibuprofen drug residue from water is carried out on composite iron nano adsorbent, which was prepared by green technology and characterized by FT-IR, XRD, SEM, TEM and EDX techniques.

Journal ArticleDOI
TL;DR: In this article, a general strategy towards designing multiresponsive, macroscopically anisotropic polymer hydrogels (MA-SPHs) with the ability of 3D complex deformations is reported.
Abstract: As one of the most promising smart materials, stimuli-responsive polymer hydrogels (SPHs) can reversibly change volume or shape in response to external stimuli They thus have shown promising applications in many fields While considerable progress of 2D deformation of SPHs has been achieved, the realization of 3D or even more complex deformation still remains a significant challenge Here, a general strategy towards designing multiresponsive, macroscopically anisotropic SPHs (MA-SPHs) with the ability of 3D complex deformations is reported Through a local UV-reduction of graphene oxide sheets (GOs) with a patterned fashion in the GO-poly(N-isopropylacrylamide) (GO-PNIPAM) composite hydrogel sheet, MA-SPHs can be achieved after the introduction of a second poly(methylacrylic acid) network in the unreduced part of GO-PNIPAM hydrogel sheet The resulting 3D MA-SPHs can provide remote-controllable light-driven, as well as thermo-, pH-, and ionic strength-triggered multiresponsive 3D complex deformations Approaches in this study may provide new insights in designing and fabricating intelligent soft materials for bioinspired applications

Journal ArticleDOI
Wenjun Jiang1, Wenjiao Luo1, Ruilong Zong1, Wenqing Yao1, Zhanping Li1, Yongfa Zhu1 
01 Aug 2016-Small
TL;DR: A new idea of the construction of 3D hierarchical photocatalysts is presented, which can be applied in the sustainability field and is highly excellent in removing organic pollutant for PANI/CNNS composite hydrogel.
Abstract: A polyaniline (PANI)/carbon nitride nanosheets (CNNS) composite hydrogel with 3D hierarchical nanostructure is synthesized via in situ polymerization. The 3D hierarchical structure is robust and stable, making the composite hydrogel separation-free and easy to recycling. It is highly excellent in removing organic pollutant for PANI/CNNS composite hydrogel on account of the cooperation of adsorptive preconcentration and the following photocatalytic oxidation. Pollutants are first adsorbed and concentrated into the 3D hierarchical nanostructure of the composite hydrogel. Then the pollutants are in situ oxidized via photocatalysis. The promoted photocatalytic performance can be mainly ascribed to the outstanding interfacial charge separation and photoelectrochemical performance. A new idea of the construction of 3D hierarchical photocatalysts is presented, which can be applied in the sustainability field.

Journal ArticleDOI
01 May 2016-Carbon
TL;DR: In this article, the authors fabricated highly self-aligned large-area reduced graphene oxide/poly (vinylidene fluoride-co-hexafluoropropylene) (rLGO/PVDF-HFP) composite films through simple solution casting followed by low temperature chemical reduction process.