This review presents the commonly used crosslinking methods for hydrogel synthesis and summarizes the current status and discusses future perspectives.

h i g h l i g h t sThe absorption, bioaccumulation, metabolism and internal exposure of OPFRs are reviewed. Inhalation, ingestion and dermal contact are the main OPFRs absorptionpathways for humans. General in vivo and in vitro metabolic pathways of three different types of OPFRs are proposed. DAPs and MAPs are considered as putative biomarkers for the assessment of internal exposure of OPFRs in humans. a r t i c l e i n f o t r a c tDue to their widespread use, organophosphate flame retardants (OPFRs) are commonly detected in various environmental matrices and have been identified as emerging contaminants. Considering the adverse effects of OPFRs, many researchers have paid their attention on the absorption, bioaccumulation, metabolism and internal exposure processes of OPFRs in animals and humans. In this article, we first review the diverse absorption routes of OPFRs by animals and humans (e.g., inhalation, ingestion, dermal absorption and gill absorption). Bioaccumulation and biomagnification potentials of OPFRs in different types of organisms and food webs are also summarized, based on quite limited available data and results. For metabolism, we review the Phase-I and Phase-II metabolic processes for each type of OPFRs (chlorinated OPFRs, alkyl-OPFRs and aryl-OPFRs) in the animals and humans, as well as toxicokinetic information and putative exposure biomarkers on OPFRs. Finally, we highlight gaps in our knowledge and critical directions for future internal exposure studies of OPFRs in animals and humans.

Conjugated microporous polymers (CMPs) have gained much recent attention as a kind of metal-free organic photocatalyst for photocatalytic hydrogen generation. However, the development of a visible-light-driven CMP photocatalyst with high photocatalytic activity is still a big challenge. Here, we report dibenzothiophene dioxide containing CMP photocatalysts and demonstrate the influence of the cross-linker length on the photocatalytic performance for hydrogen production. The most active photocatalyst of DBTD-CMP1 with a short cross-linker of benzene exhibits a high hydrogen evolution rate (HER) of 2460 μmol h–1 g–1 under visible light without Pt cocatalyst. Remarkably, the Pt-loaded DBTD-CMP1 shows an attractive HER of 9200 μmol h–1 g–1 under UV–vis light illumination. This result demonstrates that these dibenzothiophene dioxide containing CMPs are competitive with the most reported porous organic polymer photocatalysts.

Aqueous zinc (Zn) batteries (AZBs) are widely considered as a promising candidate for next‐generation energy storage owing to their excellent safety features. However, the application of a Zn anode is hindered by severe dendrite formation and side reactions. Herein, an interfacial bridged organic–inorganic hybrid protection layer (Nafion‐Zn‐X) is developed by complexing inorganic Zn‐X zeolite nanoparticles with Nafion, which shifts ion transport from channel transport in Nafion to a hopping mechanism in the organic–inorganic interface. This unique organic–inorganic structure is found to effectively suppress dendrite growth and side reactions of the Zn anode. Consequently, the Zn@Nafion‐Zn‐X composite anode delivers high coulombic efficiency (ca. 97 %), deep Zn plating/stripping (10 mAh cm−2), and long cycle life (over 10 000 cycles). By tackling the intrinsic chemical/electrochemical issues, the proposed strategy provides a versatile remedy for the limited cycle life of the Zn anode.