Short and Soft: Multidomain Organization, Tunable Dynamics, and Jamming in Suspensions of Grafted Colloidal Cylinders with a Small Aspect Ratio.

The yet virtually unexplored class of soft colloidal rods with a small aspect ratio is investigated and shown to exhibit a very rich phase and dynamic behavior, spanning from liquid to nearly melt state. Instead of the nematic order, these short and soft nanocylinders alter their organization with increasing concentration from isotropic liquid with random orientation to small domains with preferred local orientation and eventually a multidomain arrangement with a local orientational order. The latter gives rise to a kinetically suppressed state akin to structural glass with detectable terminal relaxation, which, on further increasing concentration, reveals features of hexagonally packed order as in ordered block copolymers. The respective dynamic response comprises four regimes, all above the overlapping concentration of 0.02 g/mL:(I) from 0.03 to 0.1 g/mol, the system undergoes a liquid-to-solidlike transition with a structural relaxation time that grows by 4 orders of magnitude. (II) From 0.1 to 0.2 g/mL, a dramatic slowing-down is observed and is accompanied by an evolution from isotropic to a multidomain structure. (III) Between 0.2 and 0.6 g/mol, the suspensions exhibit signatures of shell interpenetration and jamming, with the colloidal plateau modulus depending linearly on concentration. (IV) At 0.74 g/mL, in the densely jammed state, the viscoelastic signature of hexagonally packed cylinders from microphase-separated block copolymers is detected. These properties set short and soft nanocylinders apart from long colloidal rods (with a large aspect ratio) and provide insights for fundamentally understanding the physics in this intermediate soft colloidal regime and for tailoring the flow properties of nonspherical soft colloids.

Highly conductive, mechanically strong graphene monolith assembled by three-dimensional printing of large graphene oxide.

The manufacturing of three-dimensional (3D) graphene monolith with high mechanical and electrical performance has become an urgent issue in view of their potential applications in energy and electronics fields. Due to the structure rigidity and poor liquid-phase processing capability of graphene sheets, it is challenging to fabricate 3D graphene monolith with high mechanical performance, including strength, toughness and resiliency. Graphene oxide (GO) shows an improved dispersibility and reduction-restorable conductivity, which enables it to effectively balance the processing and comprehensive performances of graphene monolith. Here, we demonstrate a strategy to fabricate high-performance, shape-designable 3D graphene monolith through a 3D printing method based on large-sized graphene oxide (LGO) fluid ink. The concentration of the LGO ink for printing is as low as 20 mg/mL. The resulting monolith exhibits low density (12.8 mg/cm3), high electrical conductivity (41.1 S/m), high specific strength (10.7 × 103 N·m/Kg) and compressibility (up to 80% compressive strain). Such a 3D printing technique enables plenty of complicated monolith structures and broadens the application range of graphene.

Coating-free, air-stable silver nanowires for high-performance transparent conductive film.

Silver nanowire (Ag NW) based films are considered as a promising alternative for traditional indium tin oxide but still suffer from some limitations, including insufficient conductivity, transparency and environmental instability. We here report a novel etching synthesis strategy to improve the performance of Ag NW films. Different from the traditional methods to synthesize high aspect ratios of NWs or employ electrically conductive coatings, we find it effective to reduce the high-reactivity defects of NWs for optimizing the comprehensive performance of Ag NW films. In this strategy etching can suppress the generation of high-reactivity defects and meanwhile the etching growth of NWs can be accomplished in an uneven ligand distribution environment. The resulting Ag NWs are uniformly straight with a sharp-edged structure. The transparent conductive film obtained exhibits simultaneous improvements in electrical conductivity, transparency and air stability. Even after exposure in air for 200 days and no protective coatings, the film can still meet the highest requirement of practical applications, with a figure of merit 361 (i.e., FoM > 350). These results not only demonstrate the importance of defect control in the synthesis of Ag NWs, but also pave a way for further optimizing the performance of Ag NW-based films.

Polymer-Grafted Nanoparticles with Precisely Controlled Structures.

Polymer-tethered nanoparticles with different geometric shapes are very useful fillers of polymer nanocomposites. Herein, a universal approach for the fabrication of such nanoparticles with precisely controlled shape and composition is reported. By microphase separation of poly(3-(triethoxysilyl)propyl methacrylate)-block-polystyrene (PTEPM-b-PS) in the presence of oligomers, o-TEPM (oT) and/or o-S (oS), followed by cross-linking and dispersion in PS solvent, precisely tailored PS-grafted nanoparticles were prepared. These particles include those with varied shapes but identical PS shells, particles with varied core sizes but the same PS shell, and particles with fixed shapes but varied PS shells. These particles are ideal model nanofillers to study the dynamics and reinforced mechanism of polymer nanocomposites.