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The bonding behaviour between steel fibre and concrete matrix at elevated temperature and various loading rates was investigated. Pullout tests were carried out on the hooked-end steel fibre reinforced concrete specimen and the effects of elevated temperatures (200, 400, and 600°C) and loading rates (2, 10, and 50 mm·min−1) were considered. The ultimate bond strength and energy absorption were discussed to evaluate the bonding behaviour. The results revealed that the bonding behaviour for the case of 400°C performed best, while the bonding behaviour for the case of 600°C performed the worst. At room temperature, the bonding behaviour is similar to the case of 200°C. In addition, the higher the loading rate, the greater the fluctuation of the bond slip curve of the specimen, and higher ultimate pullout load and energy absorption may be observed.

Interventions targeting the psychological status and related symptoms of perioperative patients can accelerate recovery. Five-element music therapy, as a non-pharmacological intervention method, has gained increasing attention in perioperative patient care due to its drug-free nature, lack of side effects, strong feasibility, and significant therapeutic effects. This article provides an overview of the principles of five-element music therapy, as well as intervention strategies and application effects during the perioperative period, aiming to provide references and guidance for further clinical practice. (围手术期患者的心理状态与预后密切相关。作为一种非药物干预方法, 五行音乐疗法应用于围手术期患者的心理护理中有积极作用。本文阐述五行音乐疗法的原理, 综述其在围手术期患者中的应用, 探讨后续的研究方向, 为临床推广五行音乐疗法提供参考依据。)

Unlike bulky and rigid traditional power systems, 1D fiber batteries possess appealing features such as flexibility and adaptability, which are promising for use in wearable electronic devices. However, the performance and energy density fiber batteries are limited by the contradiction between ionic transfer and robust structure of fiber electrodes. Herein, these problems are addressed via polymer engineering to regulate the microenvironment in electrodes, realizing high‐linear‐capacity thick fiber electrodes with excellent cycling performance. The porosity of the electrodes is regulated using polymer crosslink networks designed with various components, and lithium‐ion transfer is optimized through ether‐abundant polymer chains. Furthermore, reinforced covalent bonding with carbon nanotube networks is established based on the modified functional groups of polymer networks. The multiscale optimizations of the porous structure, ionic transportation, and covalent bonding network enhance the lithium‐ion dynamics property and structural stability. Therefore, ultrahigh linear‐capacity fiber electrodes (17.8 mAh m−1) can be fabricated on a large scale and exhibit excellent stability (92.8% after 800 cycles), demonstrating obvious superiority among the reported fiber electrodes. Moreover, this study highlights the high effectiveness of polymer regulation in fiber electrodes and offers new avenues for designing next‐generation wearable energy‐storage systems. [ABSTRACT FROM AUTHOR]

Lithium metal, with ultrahigh theoretical specific capacity, is considered as an ideal anode material for the lithium‐ion batteries. However, its practical application is severely plagued by the uncontrolled formation of dendritic Li. Here, a cation‐loaded porous Mg2+‐Zeolite layer is proposed to enable the dendrite‐free deposition on the surface of Li metal anode. The skeleton channels of zeolite provide the low coordinated Li+‐solvation groups, leading to the faster desolvation process at the interface. Meanwhile, anions‐involved solvation sheath induces a stable, inorganic‐rich SEI, contributing to the uniform Li+ flux through the interface. Furthermore, the co‐deposition of sustained release Mg2+ realizes a new faster migration pathway, which proactively facilitates the uniform diffusion of Li on the lithium substrate. The synergistic modulation of these kinetic processes facilitates the homogeneous Li plating/stripping behavior. Based on this synergistic mechanism, the high‐efficiency deposition with cyclic longevity exceeding 2100 h is observed in the symmetric Li/Li cell with Mg2+‐Zeolite modified anode at 1 mA cm−2. The pouch cell matched with LiFePO4 cathode fulfills a capacity retention of 88.4% after 100 cycles at a severe current density of 1 C charge/discharge. This synergistic protective mechanism can give new guidance for realizing the safe and high‐performance Li metal batteries. [ABSTRACT FROM AUTHOR]

The practical application of aqueous zinc ion batteries is greatly hindered by the severe dendrite growth and side reactions on the Zn metal anode. To address these challenges, nanodiamond (ND) particles are implanted on the Zn foil surface by a straightforward mechanical rolling process, which serves as heterogeneous seeds, enhancing the cycling stability of Zn metal anode. ND particles with carboxyl groups facilitate the even distribution of electric fields and Zn2+ ions in their vicinity, which promotes the homogeneous deposition of Zn. Moreover, the excellent corrosion resistance of ND particles alleviates the side reactions of the electrode, thus effectively protecting the Zn metal anode in aqueous electrolyte. Benefited from these advantages, the ND@Zn anode shows over 4100 h reversible cycles in symmetric cells, and 99.7% Coulombic efficiency in asymmetric cells. The ND@Zn||MnO2 full cell achieves a stable life of 1000 cycles with 87.0% capacity retention at 1 A g−1 current density. This cost‐effective fabrication process holds the potential for scalability, making it amenable to large‐scale production of zinc metal anodes. [ABSTRACT FROM AUTHOR]

The release of flammable gases during battery thermal runaway poses a risk of combustion and explosion, endangering personnel safety. The convective and diffusive properties of the gas make it challenging to accurately measure gas state, complicating the assessment of the battery pack exhaust design. In this paper, a thermal resistance network model is established, which is used to calculate the battery thermal runaway propagation. Gas accumulation after thermal runaway venting of a LiFeO4 module is studied using ANSYS Fluent under different venting schemes. The results show that the scheme of battery inversion and simultaneous exhaust from the side and bottom of the module is optimal. The methods and results presented can guide the design of LiFeO4 cell pack runners. [ABSTRACT FROM AUTHOR]