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Three‐dimensional graphene architecture (3DGA) as reinforcement with successive reinforcement effect has attracted intense attention in the field of polymer composites, while 3DGA also faces the disadvantages of weak interfacial adhesion with matrices. The surface decoration of 3DGA with molybdenum disulfide (3DGA@MoS2) further promoted the diffusion and penetration of epoxy molecular for 3DGA network with the aid of resin transfer molding (RTM) technic. The MoS2 transition nanolayer not only forms covalent bonding with 3DGA but mechanical interlocks with epoxy, which effectively improved the interface combination in composite. Compared with neat epoxy, the glass transition temperature (Tg) and tensile strength increased by 18°C and 58.6%, as well as the average friction coefficient and wear rate decreased by 84% and 89%, respectively, by low loading of only 2 wt% 3DGA@MoS2. Hence, the 3D graphene modified strategy by surface decoration provides a new insight for manufacturing high‐performance epoxy‐graphene composites with excellent tribological properties. Highlights: A highly ordered and interconnected 3DGA reinforcement was fabricated.MoS2 serves as interlayer, forming covalent bond and mechanical interlock.Incorporation of 3DGA@MoS2 enables rapid heat conduction and load transfer.Bi‐interpenetrating 3D structure/polymer network endows good wear resistance.Improved comprehensive properties ascribe to strong interface adhesion. [ABSTRACT FROM AUTHOR]

Addition of organic compounds containing O/N heteroatoms to aqueous electrolytes such as ZnSO4 (ZS) solutions is one of the effective strategies to inhibit Zn anode dendrites and side reactions. However, addressing the stability of Zn plating/stripping at high current densities and areal capacities by this method is still a challenge, especially in capacitors known for high power and long life. Herein, an organic heterocyclic compound of 1, 4, 7, 10‐tetraazacyclododecane (TC) containing four symmetrically distributed N atoms is employed as ZS additive, expanding the life of Zn anodes from ≈ 30 h to 1000 and 240 h at deep plating/stripping conditions of 10 and 20 mA cm−2/mAh cm−2, respectively; the cumulative capacity is as high as 5.0 Ah cm−2 with 99% Coulombic efficiency, far exceeding reported additives. TC with higher binding energies than H2O for Zn species tends to adsorb to Zn (002) in a lying manner and participate in the solvation shell of Zn2+, thus avoiding Zn dendrites and side‐reaction damage, especially at high current densities. The TC‐endowed Zn anode's stability under such extreme conditions is verified in Zn‐ion capacitors (i.e., > 94.6% capacity retention after 28 000 cycles), providing new insights into the development of high‐power Zn‐based energy storage devices. [ABSTRACT FROM AUTHOR]

Electrochemical carbon dioxide reduction reaction (CO2RR) can produce value-added hydrocarbons from renewable electricity, providing a sustainable and promising approach to meet dual-carbon targets and alleviate the energy crisis. However, it is still challenging to improve the selectivity and stability of the products, especially the C2+ products. Here we propose to modulate the electronic structure of copper oxide (CuO) through lattice strain construction by zinc (Zn) doping to improve the selectivity of the catalyst to ethylene. Combined performance and in situ characterization analyses show that the compressive strain generated within the CuO lattice and the electronic structure modulation by Zn doping enhances the adsorption of the key intermediate ⋆CO, thereby increasing the intrinsic activity of CO2RR and inhibiting the hydrogen precipitation reaction. Among the best catalysts had significantly improved ethylene selectivity of 60.5% and partial current density of 500 mA·cm−2, and the highest C2+ Faraday efficiency of 71.47%. This paper provides a simple idea to study the modulation of CO2RR properties by heteroatom doped and lattice strain. [ABSTRACT FROM AUTHOR]

Concrete vibration construction sustains high labor intensity, a poor working environment, difficulties in quality control, and other problems. Current research on concrete vibration focuses on monitoring vibration quality, evaluating vibration processes quantitatively, and assessing mechanical vibration of unreinforced mesh concrete (plain concrete). Standardizing concrete vibration under reinforcing steel mesh remains difficult. There is still a lag in the evaluation of the quality of rework and the consumption of human and material resources. To tackle these issues, a vibrating robotic arm system based on automation control technology, machine vision, and kinematic modeling is proposed. Research and simulation tests on intelligent concrete vibration under reinforcing steel mesh aim to enhance construction efficiency and quality. A five-degree-of-freedom robotic arm with a vision module identifies each rebar grid center in the image, extracts the pixel coordinates, and converts them to the mechanical coordinates by the integration of machine vision algorithms. A vibrator point screening algorithm is introduced to determine actual vibrator point locations based on specific insertion spacing, alongside a vibro-module for vertical movement. Real-time assessment of vibration quality is achieved using the YOLOv5 target detection model. Simulation tests confirm the feasibility of automated concrete vibration control under reinforcing steel mesh by a vibrating robot arm system. This research offers a new approach for unmanned vibration technology in concrete under reinforcing steel mesh, supporting future related technological advancements with practical value. [ABSTRACT FROM AUTHOR]

The triboelectric nanogenerator (TENG), as a novel energy harvesting technology, has garnered widespread attention. As a relatively young field in nanogenerator research, investigations into various aspects of the TENG are still ongoing. This review summarizes the development and dissemination of the fundamental principles of triboelectricity generation. It outlines the evolution of triboelectricity principles, ranging from the fabrication of the first TENG to the selection of triboelectric materials and the confirmation of the electron cloud overlapping model. Furthermore, recent advancements in TENG application scenarios are discussed from four perspectives, along with the research progress in performance optimization through three primary approaches, highlighting their respective strengths and limitations. Finally, the paper addresses the major challenges hindering the practical application and widespread adoption of TENGs, while also providing insights into future developments. With continued research on the TENG, it is expected that these challenges can be overcome, paving the way for its extensive utilization in various real-world scenarios. [ABSTRACT FROM AUTHOR]

Low ionic concentrations and the chemical stability of the ions involved to water are considered necessary for hydrated ionic solution lubricants. Herein, an ultra-high concentration of chemically active ZnCl2 aqueous solution (up to 20 mol L− 1) is first reported to be used as a liquid superlubricant, with trace amounts of Zn2+ hydrolyzed to generate Zn(OH)2 (i.e., hard clusters) in addition to Zn2+ hydrated with water (i.e., soft clusters), resulting in the formation of heterogeneous phases with a mixture of soft and hard clusters. The coefficient of friction (COF) inversely correlates with the molar concentration of ZnCl2, where the COF of the optimized samples can be as low as 0.006 with a stable macroscopic superlubricated state; the particle size distribution of clusters and their corresponding Spans, however, are positively correlated with the molar concentration, suggesting that asymmetric contact between these unequal-sized soft and hard clusters contributes greatly to the reduction of interfacial shear resistances. This ultra-high-concentration aqueous solution superlubricant not only breaks the convention but also deepens the mechanism of liquid superlubricity from the perspectives of cluster size distribution and interactions between clusters, providing a new insight into the design of advanced water-based ionic solution superlubricants. [ABSTRACT FROM AUTHOR]

Adding additives (e.g., carbon dots, CDs) to liquid lubricants is an effective method for enhancing their load‐bearing capacity and friction reduction. However, it is challenging to simultaneously impart high load‐bearing capacity and superlubricity for them (e.g., ionic liquid analogs, ILAs) through this strategy due to strong Coulombic interactions. With CDs as a competing ligand operon, the cluster size distribution can be expanded, conferring superlubricity with ultrahigh load‐bearing capacity (>705 MPa, the highest value of CDs‐based superlubricious materials thus far) for CDs/ILAs. In particular, methodologies such as Raman, 1H‐NMR, fourier transform infrared spectroscopy, and laser particle size analysis are employed to characterize the evolution of their H‐bonding interactions and particle size distribution. CDs can act as competing ligands and enable CDs/ILAs to form systems with ultra‐low coefficient of friction and wear consisting of a mixture of large and small clusters. The mixed and expanded size clusters facilitate the reduction of the viscosity for CDs/ILAs under shear, thereby reducing the interfacial shear resistance during superlubricity, while the CDs within them efficiently transfer the normal bearing loads. The progress is made from the perspective of cluster particle size distribution rather than individual additive properties, providing a new avenue for designing ILAs‐based superlubricious materials. [ABSTRACT FROM AUTHOR]

Carbon‐based supercapacitors are one of the most widely used commercial products. Organic electrolyte systems, such as tetraethylammonium tetrafluoroborate/acetonitrile (TEABF4/ACN), remain dominant after decades of development due to cost and performance advantages. However, improving the capacitance of existing carbon‐electrolyte systems not by altering the pore structure and surface properties of activated carbon is full of challenges. Herein, a non‐Faraday organic ferroelectric salt additive (diisopropylamine perchlorate, DIPAP) that can significantly increase capacitance from the standpoint of electrolyte dielectric modulation is proposed for the first time. Compared to counter ions, DIPA+ plays a vital role in capacity enhancement, in which electron‐rich N‐doped mesoporous carbon can greatly boost capacity by promoting local ion mobility. In situ Raman and theoretical studies show that small‐size DIPA+ can enter the pore and be enriched closer to electrode surfaces than TEA+ and ACN, allowing it to regulate the distribution of electric double‐layer species and dielectric properties (i.e., effective thickness of dielectric and/or relative dielectric constant), increasing capacity by up to 21.6–45.8% with only 1 wt% DIPAP while maintaining desired rate performances. The understanding of the mechanism of capacitance increase by such additives opens up new avenues for further extension of the commercialized carbon electrode‐organic electrolyte system's potential. [ABSTRACT FROM AUTHOR]

Background: In patients with facial paralysis, the free functional gracilis muscle transfer is preferred for facial reanimation. The choice of an adequate motor nerve to innervate the transplanted gracilis muscle is one of the procedure's key components. We present a comparative study between cross-facial nerve graft (CFNG) and masseteric nerve as donor nerves for reinnervated gracilis flap transfer in patients with complete facial paralysis., Materlals and Methods: Retrospective analysis was performed on all patients with complete facial paralysis who had a free functional gracilis muscle transfer for facial reanimation between January 2014 and December 2021. Only those who received gracilis transfer reinnervated by either CFNG or masseteric nerve were included in this study. The smile excursion and lip angle were measured for evaluating the outcomes postoperatively., Results: The inclusion criteria were met by a total of 21 free functional gracilis muscle transfers, of which 11 were innervated by CFNG and 10 by the masseteric nerve. Both surgical procedures resulted in a highly considerable smile excursion of the reanimated side and postoperative improvement of static or dynamic lip angle. Masseteric nerve coaptation led to greater smile excursion and more significant improvement of dynamic lip angle than CFNG., Conclusions: For patients who have complete facial paralysis, face reanimation can be successfully accomplished by free gracilis transfer reinnervated by the CFNG or the masseteric nerve. In particular, the masseteric nerve is a reliable choice for dynamic smile reanimation., Competing Interests: The authors report no conflicts of interest., (Copyright © 2023 by Mutaz B. Habal, MD.)