Sustainable hydrogen production via water electrolysis is pivotal to addressing global energy and environmental challenges. Among emerging materials, quantum dots (QDs) have garnered significant attention for the hydrogen evolution reaction (HER) due to their zero-dimensional nanostructure, high specific surface area, tunable electronic characteristics, and abundant active sites. This review provides a comprehensive overview of recent advancements in QD-based catalysts for electrocatalytic HER, focusing on the fundamental mechanisms that drive their enhanced performance. Key enhancement strategies—such as substrate dispersion, surface functionalization, defect engineering, and heteroatom doping—are critically discussed. Furthermore, the review explores the potential of QD-based catalysts for large-scale and industrial applications. By synthesizing current progress and challenges, this review offers critical insights into the rational design of next-generation HER catalysts to advance sustainable hydrogen energy.

The primary challenges posed by oral mucosal diseases are their high incidence and the difficulty in managing symptoms. Inspired by the ability of bioelectricity to activate cells, accelerate metabolism, and enhance immunity, a conductive polyacrylamide/sodium alginate crosslinked hydrogel composite containing reduced graphene oxide (PAA-SA@rGO) is developed. This composite possesses antibacterial, anti-inflammatory, and antioxidant properties, serving as a bridge to turn the “short circuit” of the injured site into a “completed circuit,” thereby prompting fibroblasts in proximity to the wound site to secrete growth factors and expedite tissue regeneration. Simultaneously, the PAA-SA@rGO hydrogel effectively seals wounds to form a barrier, exhibits antibacterial and anti-inflammatory properties, and prevents foreign bacterial invasion. As the electric field of the wound is rebuilt and repaired by the PAA-SA@rGO hydrogel, a 5 × 5 mm² wound in the full-thickness buccal mucosa of rats can be expeditiously mended within mere 7 days. The theoretical calculations indicate that the PAA-SA@rGO hydrogel can aggregate and express SOX2, PITX1, and PITX2 at the wound site, which has a promoting effect on rapid wound healing. Importantly, this PAA-SA@rGO hydrogel has a fast curative effect and only needs to be applied for the first three days, which significantly improves patient satisfaction during treatment.

The natural design and coupling of biological structures are the root of realizing the high strength, toughness, and unique functional properties of biomaterials. Advanced architecture design is applied to many materials, including metal materials, inorganic nonmetallic materials, polymer materials, and so on. To improve the performance of advanced materials, the designed architecture can be enhanced by bionics of biological structure, optimization of structural parameters, and coupling of multiple types of structures. Herein, the progress of structural materials is reviewed, the strengthening mechanisms of different types of structures are highlighted, and the impact of architecture design on the performance of advanced materials is discussed. Architecture design can improve the properties of materials at the micro level, such as mechanical, electrical, and thermal conductivity. The synergistic effect of structure makes traditional materials move toward advanced functional materials, thus enriching the macroproperties of materials. Finally, the challenges and opportunities of structural innovation of advanced materials in improving material properties are discussed.

In recent years, various functional fabrics capable of responding to multistimuli have been widely recognized as promising wearable devices. However, the obtained composite functional fabrics have only been applied in a few scenarios, rendering the achievement of multifunctional wearable application scenarios a difficult goal. Therefore, there is an urgent need to expand the diversity of wearable applications for functional fabrics. Herein, we design hydrogel composite fabrics capable of responding to multiple stimuli, including vibration, temperature, strain, and pressure, to enable wearable multiapplication scenarios. The hydrogel composite fabrics, based on nylon fabrics (NFs), are fabricated with polyacrylamide (PAM)-poly(vinyl alcohol) (PVA)-sodium alginate (SA)-reduced graphene oxide (rGO)/NFs (PAM-PVA-SA-rGO/NFs). The PAM-PVA-SA-rGO/NFs exhibit a higher elastic stiffness coefficient (2.79 N cm^-1) than the blank NFs (1.76 N cm^-1), good temperature sensitivity in the range of 30-80 °C, and excellent detecting ability for urine presence with a threshold of unit area of 2.55 × 10^-3 mL cm^-2. The PAM-PVA-SA-rGO/NFs can not only respond to multiple stimuli but also be integrated into clothing for wearable multiapplication scenarios, such as detecting human speaking and breathing, intelligent sleeves, and diaper alarms. Additionally, the mechanisms of the above phenomena are revealed. These results indicate that the PAM-PVA-SA-rGO/NFs will provide inspiration for the development of intelligence systems, feedback devices, soft robotics, wearable devices, etc.

All-solid-state sodium-ion battery (ASSIB) is a promising new energy storage device due to the excellent thermal stability, low flammability, high impermeability and nonvolatility, as well as riskless fire and explosion properties. The solid electrolyte plays a core role in the ASSIBs to determine their electrochemical performance. Herein, close attention is paid to effective approaches to improve the performance of solid electrolytes, including ion doping and substitution, composite method, coating method, crystal transformation method, ceramization and vitrification, etc. In particular, electrochemical window, ionic conductivity, electrochemical stability, and structural stability are also reviewed. The future development of solid electrolytes and the possible directions for improving the properties of the ASSIBs in practical applications are also prospects. This review will guide the development of solid electrolytes for the ASSIBs in future.

All-solid-state sodium-ion batteries (SIBs) possess the advantages of rich resources, low price, and high security, which are one of the best alternatives for large-scale energy storage systems in the future. Also, the chalcogenide solid electrolytes (CSEs) of SIBs have the characteristics of excellent room-temperature ionic conductivity (10⁻³-10⁻² S cm⁻¹), low activation energy (<0.6 eV), easy cold-pressing consolidation, etc. Hence, CSEs have become a very active area of all-solid-state SIB research in recent years. In this review, the modification methods and implementation technologies of CSEs are summarized, and the structure and electrochemical performance of the CSEs are discussed. Furthermore, the auxiliary function of first-principle calculations for modification is introduced. Ultimately, we describe the challenges regarding CSEs and propose some strategic suggestions.