carrier with an extremely high energy density (approximately 142 MJ kg −1 ) and zero-carbon content, has been regarded as a promising clean fuel. [1,2] In this context, electrochemical water splitting, which converts electricity into storable hydrogen, is a viable and efficient solution to mitigate severe energy shortages and greenhouse gas emissions. [3] Among these strategies, hydrogen and oxygen evolution reactions, which occur on the cathode and anode, respectively, in a water electrolyzer, are considered as two critical half-reactions of the water-splitting process. [4] Theoretically, water splitting requires a thermodynamic Gibbs free energy (ΔG) of approximately 237.2 kJ mol −1 , corresponding to a standard potential (ΔE) of 1.23 V versus a reversible hydrogen electrode (RHE), which allows the thermodynamically uphill reaction to occur in the electrolyzer. [5] However, the unfavorable thermodynamics and resulting large overpotential are the main barriers to the scalable implementation of water electrolysis for hydrogen generation. [6,7] Currently, noble metal-based electrocatalysts exhibit the most efficient activity for water splitting, particularly Pt-based hydrogen evolution reaction (HER) catalysts and Ir/Ru-based oxygen evolution reaction (OER) catalysts. [8,9] Nevertheless, the scarcity and high price of precious metals severely impede their widespread use in commercial water-splitting applications. Taking these limitations into Electrochemical water splitting has attracted significant attention as a key pathway for the development of renewable energy systems. Fabricating efficient electrocatalysts for these processes is intensely desired to reduce their overpotentials and facilitate practical applications. Recently, metal-organic framework (MOF) nanoarchitectures featuring ultrahigh surface areas, tunable nanostructures, and excellent porosities have emerged as promising materials for the development of highly active catalysts for electrochemical water splitting. Herein, the most pivotal advances in recent research on engineering MOF nanoarchitectures for efficient electrochemical water splitting are presented. First, the design of catalytic centers for MOF-based/derived electrocatalysts is summarized and compared from the aspects of chemical composition optimization and structural functionalization at the atomic and molecular levels. Subsequently, the fast-growing breakthroughs in catalytic activities, identification of highly active sites, and fundamental mechanisms are thoroughly discussed. Finally, a comprehensive commentary on the current primary challenges and future perspectives in water splitting and its commercialization for hydrogen production is provided. Hereby, new insights into the synthetic principles and electrocatalysis for designing MOF nanoarchitectures for the practical utilization of water splitting are offered, thus further promoting their future prosperity for a wide range of applications.

Vitiligo is an autoimmune cutaneous disease in which melanocytes are destroyed by CD8 + T cells resulting in disfiguring white spots. From the very beginning of the disease, oxidative stress plays a significant role in promoting the onset of vitiligo, as noted by many studies. Multiple factors lead to the overproduction of reactive oxygen species (ROS), and collaboratively cause ROS accumulation in vulnerable melanocytes. However, ROS are responsible for melanocyte damage manifested by the level of molecules, organelles, and cells, and the generation of autoantigens, through different pathways related to the dysregulation of melanocytes. Recent studies have shown that presentation of autoantigens is mediated by innate immunity, which bridges the gap between oxidative stress and adaptive immunity. The recruitment of CD8 + T cells induced by cytokines and chemokines guarantees the final destruction of epidermal melanocytes. Moreover, emerging concerns regarding regulatory T cells and resident memory T cells help explain the reinstatement and relapse of vitiligo. Here, we provide new perspectives in the advances in understanding of this disease pathogenesis and we attempt to find more interrelationships between oxidative stress and autoimmunity.

Moso bamboo is recognized as phytoremediation plant due to production of huge biomass and high tolerance in stressed environment. Hydroponics and pot experiments were conducted to investigate mechanism of copper tolerance and to evaluate copper accumulation capacity of Moso bamboo. In hydroponics experiment there was non significant variation in MDA contents of leaves compared with control. SOD and POD initially indicated enhancing trend with application of 5 μM Cu and then decreased consistently with application of 25 and 100 μM Cu. Application of each additional increment of copper have constantly enhanced proline contents while maximum increase of proline was observed with application of 100 μM copper. In pot experiment chlorophyll and biomass initially showed increasing tendency and decreased gradually with application of each additional increment of Cu. Normal growth of Moso bamboo was observed with application of 100 mg kg−1 copper. However, additional application of 300 or 600 mg kg−1 copper had significantly inhibited growth of Moso bamboo. The concentration of Cu in Moso bamboo has attained the levels of 340, 60, 23 mg kg−1 in roots, stems and leaves respectively. The vacuoles were the main organs which accumulated copper and reduced toxicity of copper as studied by TEM-DEX technology.

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Bio-inspired by spider silk, we simultaneously integrated high strength and toughness to PVA/TA films via extensive hydrogen bonding interactions.

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High strength composite fibers were prepared from poly(vinyl alcohol) (PVA) (degree of polymerization: 6100) reinforced by reduced graphene oxide (rGO).