Adhesive hydrogels have gained popularity in biomedical applications, however, traditional adhesive hydrogels often exhibit short-term adhesiveness, poor mechanical properties and lack of antibacterial ability. Here, a plant-inspired adhesive hydrogel has been developed based on Ag-Lignin nanoparticles (NPs)triggered dynamic redox catechol chemistry. Ag-Lignin NPs construct the dynamic catechol redox system, which creates long-lasting reductive-oxidative environment inner hydrogel networks. This redox system, generating catechol groups continuously, endows the hydrogel with long-term and repeatable adhesiveness. Furthermore, Ag-Lignin NPs generate free radicals and trigger self-gelation of the hydrogel under ambient environment. This hydrogel presents high toughness for the existence of covalent and non-covalent interaction in the hydrogel networks. The hydrogel also possesses good cell affinity and high antibacterial activity due to the catechol groups and bactericidal ability of Ag-Lignin NPs. This study proposes a strategy to design tough and adhesive hydrogels based on dynamic plant catechol chemistry.

In order to make full utilization of the high intrinsic surface area of graphene, recently, porous graphene materials including graphene nanomesh, crumpled graphene and graphene foam, have attracted tremendous attention and research interest, owing to their exceptional porous structure (high surface area, and high pore volume) in combination with the inherent properties of graphene, such as high electronic conductivity, good thermal stability, and excellent mechanical strength. Interestingly, porous graphene materials and their derivatives have been explored in a wide range of applications in the fields of electronic and photonic devices, energy storage, gas separation/storage, oil absorption and sensors. This article reviews recent progress in the synthesis, characterization, properties, and applications of porous graphene materials. We aim to highlight the importance of designing different porous structures of graphene to meet future challenges, and the trend on future design of porous graphene materials is analyzed.

We demonstrated the fabrication of functionalized graphene nanosheets via low temperature (300 °C) treatment of graphite oxide with a slow heating rate using Mg(OH)2 nanosheets as template. Because of its dented sheet with high surface area, a certain amount of oxygen-containing groups, and low pore volume, the as-obtained graphene delivers both ultrahigh specific gravimetric and volumetric capacitances of 456 F g(-1) and 470 F cm(-3), almost 3.7 times and 3.3 times higher than hydrazine reduced graphene, respectively. Especially, the obtained volumetric capacitance is the highest value so far reported for carbon materials in aqueous electrolytes. More importantly, the assembled supercapacitor exhibits an ultrahigh volumetric energy density of 27.2 Wh L(-1), which is among the highest values for carbon materials in aqueous electrolytes, as well as excellent cycling stability with 134% of its initial capacitance after 10,000 cycles. Therefore, the present work holds a great promise for future design and large-scale production of high performance graphene electrodes for portable energy storage devices.

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Fundamentals, challenges, and solutions towards fast-charging graphite anodes are summarized in this review, with insights into the future research and development to enable batteries suitable for fast-charging application.