Morphology modulation of artificial muscles by thermodynamic-twist coupling.

Human muscles can grow and change their length with body development; therefore, artificial muscles that modulate their morphology according to changing needs are needed. In this paper, we report a strategy to transform an artificial muscle into a new muscle with a different morphology by thermodynamic-twist coupling, and illustrate its structural evolution during actuation. The muscle length can be continuously modulated over a large temperature range, and actuation occurs by continuously changing the temperature. This strategy is applicable to different actuation modes, including tensile elongation, tensile contraction and torsional rotation. This is realized by twist insertion into a fibre to produce torsional stress. Fibre annealing causes partial thermodynamic relaxation of the spiral molecular chains, which serves as internal tethering and inhibits fibre twist release, thus producing a self-supporting artificial muscle that actuates under heating. At a sufficiently high temperature, further relaxation of the spiral molecular chains occurs, resulting in a new muscle with a different length. A structural study provides an understanding of the thermodynamic-twist coupling. This work provides a new design strategy for intelligent materials.

An interfacially polymerized self-healing organo/hydro copolymer with shape memory.

Organo/hydro copolymer materials have recently received significant attention in the fields of energy, environment and healthcare. Herein, we report the fabrication of a robust organo/hydro copolymer with rapid self-healing and shape memory by emulsion interfacial polymerization. The emulsion interfacial polymerization allowed the formation of a crosslinked organo/hydro copolymer with hydrogen-bonded networks, significantly enhancing the mechanical properties; the proposed organo/hydro copolymer substantially outperformed most of the synthetic self-healing polymers based on hydrogen bonding interactions. We showed that the interfacially polymerized organo/hydro copolymer exhibited good self-healing capacity, i.e. achieved self-healing in less than 2 h, with a healing efficiency of 95.6%. Moreover, it presented shape memory, with a complete shape memory time less than 5 min.

One-step green synthesis of composition-tunable Pt-Cu alloy nanowire networks with high catalytic activity for 4-nitrophenol reduction.

Controlling the structure, morphology, and composition of noble metals is of great significance to improve the catalytic activity and stability of catalysts. Herein, we have successfully synthesized self-interconnecting Pt-Cu alloy nanowire networks (NWNs) with controllable compositions via the co-reduction of the metal precursors potassium chloroplatinate (K2PtCl6) and CuCl2 with sodium borohydride (NaBH4). Owing to the hydrogen bubbles formed by NaBH4 hydrolysis and oxidation as a dynamic template, the facile strategy was carried out without any organic solvent, capping agent, polymer, or special experimental device, ensuring that the surfaces of NWNs were definitely "clean". The performance of the as-prepared Pt-Cu alloy NWNs for the reduction of 4-NP was dramatically improved compared with that of pure Pt NWNs and the commercial Pt/C catalyst. Particularly, the PtCu NWNs with a Pt/Cu atomic ratio of 1 : 1 exhibited excellent catalytic activity and reusability for the reduction of toxic 4-NP. The reaction rate constant and activity factor of the PtCu NWNs reached 1.339 × 10-2 s-1 and 66.95 s-1 g-1, respectively, which were dramatically better than those of pure Pt NWNs (11.5-fold) and commercial Pt/C (13-fold). The superior catalytic activity and reusability can mainly be attributed to the clean surface, the synergistic effect of Cu and Pt atoms and the self-interconnecting nanowire network structure.

Rational Design and Synthesis of Carboxylate Gemini Surfactants with an Excellent Aggregate Behavior for Nano-La2O3 Morphology-Controllable Preparation.

A series of carboxylate gemini surfactants (CGS, Cn-Φ-Cn, n = 12, 14, 16, 18) with diphenyl ketone as a spacer group were prepared using a simple and feasible synthetic method. These CGS exhibited an excellent surface activity with extremely low critical micelle concentration (CMC) value (approximately 10-5 mol/L), good performance in reducing surface tension (nearly 30 mN/m), and the ability of molecular self-assembly into different aggregate morphologies via adjusting the concentrations, which is attributed to the introduction of diphenyl ketone and carboxylic acid ammonium salt in the molecular structure. Moreover, the surface activity and self-assembly ability of CGS were further optimized by tuning the length of the tail chain. These excellent properties imply that CGS can be a soft template to prepare nanomaterials, especially in morphology-controllable synthesis. By adjusting the concentration of one of CGS (C12-Φ-C12), nano-La2O3 particles with diverse morphologies were obtained, including spherical shape, bead-chain shape, rod shape, velvet-antler shape, cedar shape, and bowknot shape. This work offers a vital insight into the rational design of template agents for the development of morphology-controllable nanomaterials.

A facile fabrication of amphiphilic Janus and hollow latex particles by controlling multistage emulsion polymerization.

In this paper, we found that morphology controllable compound latex particles could be prepared by controlling the multistage emulsion polymerization. Influences of the content of methacrylic acid (MAA) on preparing the hydrophilic cores and the particles were investigated with the observation of dynamic light scattering (DLS) and transmission electron microscope (TEM) results. The acorn-like latex particles were synthesized by partially encapsulated with hydrophobic polystyrene (PSt)-layer. With adding moderate polarity polymethylmethacrylate (PMMA) interlayer, the hydrophilic cores could be fully encapsulated by the hydrophobic PSt-layer, and the core-shell structure formed. After alkali treatment, the acorn-like and core-shell latex particles evolved into amphiphilic Janus and hollow latex particles, respectively. The morphology of latex particles was investigated by TEM, and the forming mechanism of amphiphilic Janus and hollow latex particles was proposed.