Robust, Ultrafast and Reversible Photoswitching in Bulk Polymers Enabled by Octupolar Molecule Design.

Improving the photoswitching rate and robustness of photochromic molecules in bulk solids is paramount for practical applications but remains an on-going challenge. Here, we introduce an octupolar design paradigm to develop a new family of visible light organic photoswitches, namely multi-branched octupolar Stenhouse Adducts (MOPSAs) featuring a C3-symmetrical A3-(D-core) architecture with a dipolar donor-acceptor (D-A) photochrome in each branch. Our design couples multi-dimensional geometric and electronic effects of MOPSAs to enable robust ultrafast reversible photoswitching in bulk polymers. Specifically, the optimal MOPSA (4 wt %) in commercial polyurethane films accomplishes nearly 100 % discoloration in 6 s under visible light with ∼ 100 % thermal-recovery in 17.4 s at 60 °C, while the acquired kinetics constants are 3∼7 times that of dipolar DASA counterpart and 1∼2 orders of magnitude higher than those of reported DASAs in polymers. Importantly, the MOPSA-doped polymer films sustain 500 discoloration/recovery cycles with slow degradation, superior to the existing DASAs in polymers (≤30 cycles). We discover that multi-dipolar coupling in MOPSA enables enhanced polarization and electron delocalization, promoting the rate-determining thermal cyclization, while the branched and non-planar geometry of MOPSA induces large free volume to facilitate the isomerization. This design can be extended to develop spiropyran or azobenzene-based ultrafast photochromic films. The superior photoswitching performance of MOPSAs together with their high-yield and scalable synthesis and facile film processing inspires us to explore their versatile uses as smart inks or labels for time-temperature indicators, optical logic encryption and multi-levelled data encryption.

Photo-Assisted Metal-Air Batteries: Recent Progress, Challenges and Opportunities.

To meet the need of high energy density, long durability, safe and cost-efficient energy conversion and storage devices, metal-air batteries like Li-O2 and Zn-O2 batteries have received enormous attention and were subject to exciting development in the past decade. Photo-assisted strategies that enable the effective combination of photo/electric energy conversion/storage render a new dimension for the conventional metal-air batteries techniques with mere electric energy utilization. Therefore, tremendous research is ongoing in search of more efficient and durable devices with photo-assisted strategies. This review provides an overview of photo-assisted Li-O2 batteries, Zn-O2 batteries, and batteries with various metal/air components. The working mechanism, the basic device architecture and practical performances of various photo-assisted systems are summarized and discussed. Furthermore, certain technical challenges and future opportunities for the photo-assisted metal air batteries are emphasized and discussed in the hope of stimulating further research.

Elongational Flow Field Processed Ultrahigh Molecular Weight Polyethylene/Polypropylene Blends with Distinct Interlayer Phase for Enhanced Tribological Properties.

Herein, we produced a series of ultrahigh molecular weight polyethylene/polypropylene (UHMWPE/PP) blends by elongational-flow-field dominated eccentric rotor extruder (ERE) and shear-flow-field dominated twin screw extruder (TSE) respectively and presented a detailed comparative study on microstructures and tribological properties of UHMWPE/PP by different processing modes. Compared with the shear flow field in TSE, the elongational flow field in ERE facilitates the dispersion of PP in the UHMWPE matrix and promotes the interdiffusion of UHMWPE and PP molecular chains. For the first time, we discovered the presence of the interlayer phase in blends with different processing modes by using Raman mapping inspection. The elongational flow field introduces strong interaction to enable excellent compatibility of UHMWPE and PP and induces more pronounced interlayer phase with respect to the shear flow field, eventually endowing UHMWPE/PP with improved wear resistance. The optimized UHMWPE/PP (85/15) blend processed by ERE displayed higher tensile strength (25.3 MPa), higher elongation at break (341.77%) and lower wear loss of ERE-85/15 (1.5 mg) compared to the blend created by TSE. By systematically investigating the microstructures and mechanical properties of blends, we found that with increased content of PP, the wear mechanism of blends varies from abrasive wear, fatigue wear, to adhesion wear as the dominant mechanism for two processing modes.

Recent Advances in Elongational Flow Dominated Polymer Processing Technologies.

The continuous development of plasticizing conveying methods and devices has been carried out to meet the needs of the polymer processing industry. As compared to the conventional shear-flow-dominated plasticizing and conveying techniques, a new method for processing polymers based on elongational flow was proposed. This new method and the related devices such as vane extruders, eccentric rotor extruders and so on, exhibited multiple advantages including shorter processing time, higher mixing effectiveness, improved product performance and better adaptability to various material systems. The development of new techniques in the field of polymer material processing has opened up a broad space for the development of new plastic products, improved product performance and reduced processing costs. In this review, recent advances concerning the processing techniques based on elongational flow are summarized, and the broad applications in polymer processing as well as some future opportunities and challenges in this vibrant area are elucidated in detail.

Erratum: In Situ Activating Strategy to Significantly Boost Oxygen Electrocatalysis of Commercial Carbon Cloth for Flexible and Rechargeable Zn-Air Batteries.

[This corrects the article DOI: 10.1002/advs.201800760.].

Structural Color Materials for Optical Anticounterfeiting.

The counterfeiting of goods is growing worldwide, affecting practically any marketable item ranging from consumer goods to human health. Anticounterfeiting is essential for authentication, currency, and security. Anticounterfeiting tags based on structural color materials have enjoyed worldwide and long-term commercial success due to their inexpensive production and exceptional ease of percept. However, conventional anticounterfeiting tags of holographic gratings can be readily copied or imitated. Much progress has been made recently to overcome this limitation by employing sufficient complexity and stimuli-responsive ability into the structural color materials. Moreover, traditional processing methods of structural color tags are mainly based on photolithography and nanoimprinting, while new processing methods such as the inkless printing and additive manufacturing have been developed, enabling massive scale up fabrication of novel structural color security engineering. This review presents recent breakthroughs in structural color materials, and their applications in optical encryption and anticounterfeiting are discussed in detail. Special attention is given to the unique structures for optical anticounterfeiting techniques and their optical aspects for encryption. Finally, emerging research directions and current challenges in optical encryption technologies using structural color materials is presented.

Donor-Acceptor Nanocarbon Ensembles to Boost Metal-Free All-pH Hydrogen Evolution Catalysis by Combined Surface and Dual Electronic Modulation.

A combined surface and dual electronic modulation strategy is used to realize metal-free all-pH catalysis towards the hydrogen evolution reaction (HER) by coupling a N-doped carbon framework (MHCF, electron acceptors) derived from MOFs with higher-Fermi-level pure carbon nanotubes (CNTs, electron donors), followed by surface modification with carboxyl-group-rich polymers. Although the three constituents are inactive, as-assembled ternary membranes yield superior HER performance with low overpotentials and high durability (≤5 % activity loss over 100 h) at all pH values. The C adjacent to pyrrolic N in MHCF is the most active site and the induced directional interfacial electron transfer from CNTs to MHCF coupled with N-driven intramolecular electron transfer in MHCF optimizes Gibbs free energy for hydrogen adsorption (ΔGH* ) near zero, while the polymer modulation enables local H+ enrichment in acidic media and enhanced water adsorption and activation in neutral and basic media.

Ultrathin Black Phosphorus-on-Nitrogen Doped Graphene for Efficient Overall Water Splitting: Dual Modulation Roles of Directional Interfacial Charge Transfer.

Few-layered exfoliated black phosphorus (EBP) has attracted surging interest for electronics, optoelectronics, and catalysis. As compared to excellent progress in electronic and optoelectronic applications, very few reports are available for electrocatalysis by metal-free EBPs. Herein, we couple solution-processable ultrathin EBP nanosheets with higher Fermi level of N-doped graphene (NG) into a new metal-free 2D/2D heterostructure (EBP@NG) with well-designed interfaces and unique electronic configuration, as efficient and durable bifunctional catalysts toward hydrogen evolution and oxygen evolution reactions (HER/OER) for overall water splitting in alkaline media. By rational interface engineering, the synergy of EBP and NG is fully exploited, which not only improves the stability of EBP, but also effectively modulates electronic structures of each component to boost their intrinsic activities. Specifically, due to the lower Fermi level of EBP relative to NG, their electronic interaction induces directional interfacial electron transfer, which not only enriches the electron density over EBP and optimizes H adsorption/desorption to promote HER, but also introduces abundant positively charged carbon sites on NG and provides favorable formation of key OER intermediates (OOH*) to improve OER energetics. Thus, despite that pure EBP or NG alone has poor or negligible activity, EBP@NG achieves remarkably enhanced bifunctional HER/OER activities, along with an excellent durability. This endows an optimized electrolyzer using EBP@NG as anode and cathode with a low cell voltage of 1.54 V at 10 mA cm-2, which is smaller than that of the costly integrated Pt/C@RuO2 couple (1.60 V).

In Situ Activating Strategy to Significantly Boost Oxygen Electrocatalysis of Commercial Carbon Cloth for Flexible and Rechargeable Zn-Air Batteries.

An in situ strategy to simultaneously boost oxygen reduction and oxygen evolution (ORR/OER) activities of commercial carbon textiles is reported and the direct use of such ubiquitous raw material as low-cost, efficient, robust, self-supporting, and bifunctional air electrodes in rechargeable Zn-air batteries is demonstrated. This strategy not only furnishes carbon textiles with a large surface area and hierarchical meso-microporosity, but also enables efficient dual-doping of N and S into carbon skeletons while retaining high conductivity and stable monolithic structures. Thus, although original carbon textile has rather poor catalytic activity, the activated textiles without loading other active materials yield effective ORR/OER bifunctionality and stability with a much lower reversible overpotential (0.87 V) than those of Pt/C (1.10 V) and RuO2 (1.02 V) and many reported metal-free bifunctional catalysts. Importantly, they can concurrently function as current collectors and as ORR/OER catalysts for rechargeable aqueous and flexible solid-state Zn-air batteries, showing excellent cell performance, long lifetime, and high flexibility.

Self-Assembled Graphene-Based Architectures and Their Applications.

Due to unique planar structures and remarkable thermal, electronic, and mechanical properties, chemically modified graphenes (CMGs) such as graphene oxides, reduced graphene oxides, and the related derivatives are recognized as the attractive building blocks for "bottom-up" nanotechnology, while self-assembly of CMGs has emerged as one of the most promising approaches to construct advanced functional materials/systems based on graphene. By virtue of a variety of noncovalent forces like hydrogen bonding, van der Waals interaction, metal-to-ligand bonds, electrostatic attraction, hydrophobic-hydrophilic interactions, and π-π interactions, the CMGs bearing various functional groups are highly desirable for the assemblies with themselves and a variety of organic and/or inorganic species which can yield various hierarchical nanostructures and macroscopic composites endowed with unique structures, properties, and functions for widespread technological applications such as electronics, optoelectronics, electrocatalysis/photocatalysis, environment, and energy storage and conversion. In this review, significant recent advances concerning the self-assembly of CMGs are summarized, and the broad applications of self-assembled graphene-based materials as well as some future opportunities and challenges in this vibrant area are elucidated.

A General Electrode Design Strategy for Flexible Fiber Micro-Pseudocapacitors Combining Ultrahigh Energy and Power Delivery.

Herein, a general strategy is proposed to boost the energy storage capability of pseudocapacitive materials (i.e., MnO2) to their theoretical limits in unconventional 1D fiber configuration by rationally designing bicontinuous porous Ni skeleton@metal wire "sheath-core" metallic scaffold as a versatile host. As a proof of concept, the 1D metallic scaffold supported-MnO2 fiber electrode is demonstrated. The proposed "sheath" design not only affords large electrode surface area with ordered macropores for large electrolyte-ion accessibility and high electroactive material loading, but also renders interconnected porous metallic skeleton for efficient electronic and ionic transport, while the metallic "core" functions as an extra current collector to promote long-distance electron transport and electron collection. Benefiting from all these merits, the optimized fiber electrode yields unprecedented specific areal capacitance of 1303.6 mF cm-2 (1278 F g-1 based on MnO2, approaching the theoretical value of 1370 F g-1) in liquid KOH and 847.22 mF cm-2 in polyvinyl alcohol (PVA)/KOH gel electrolyte, 2-350 times of previously reported fiber electrodes. The solid-state fiber micro-pseudocapacitors simultaneously achieve remarkable areal energy and power densities of 18.83 µWh cm-2 and 16.33 mW cm-2, greatly exceeding the existing symmetric fiber supercapacitors, together with long cycle life and high rate capability.

One-Pot Large-Scale Synthesis of Carbon Quantum Dots: Efficient Cathode Interlayers for Polymer Solar Cells.

Cathode interlayers (CILs) with low-cost, low-toxicity, and excellent cathode modification ability are necessary for the large-scale industrialization of polymer solar cells (PSCs). In this contribution, we demonstrated one-pot synthesized carbon quantum dots (C-dots) with high production to serve as efficient CIL for inverted PSCs. The C-dots were synthesized by a facile, economical microwave pyrolysis in a household microwave oven within 7 min. Ultraviolet photoelectron spectroscopy (UPS) studies showed that the C-dots possessed the ability to form a dipole at the interface, resulting in the decrease of the work function (WF) of cathode. External quantum efficiency (EQE) measurements and 2D excitation-emission topographical maps revealed that the C-dots down-shifted the high energy near-ultraviolet light to low energy visible light to generate more photocurrent. Remarkably improvement of power conversion efficiency (PCE) was attained by incorporation of C-dots as CIL. The PCE was boosted up from 4.14% to 8.13% with C-dots as CIL, which is one of the best efficiency for i-PSCs used carbon based materials as interlayers. These results demonstrated that C-dots can be a potential candidate for future low cost and large area PSCs producing.