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Novel Fe N C electrocatalysts derived from conjugated microporous polymers based on pre-functionalization of monomers was developed, which exhibits great potential for cathodic oxygen reduction reaction in fuel cell and provides a feasible strategy of developing multi-atoms doping catalysts for heterogeneous catalysis. [Display omitted] Porous iron–nitrogen-doped carbons (Fe N C) offer a great platform for construction of cathodic oxygen reduction reaction (ORR) catalysts in fuel cells. However, challenges still remain regarding with the collapse of carbon-skeleton during pyrolysis, uneven distribution of active sites and aggregation of metal atoms. In this work, we synthesized Fe, N co-doped conjugated microporous polymer (FeN-CMP) through a facile bottom-up strategy using 1,3,5-triethynylbenzene and iron-chelated 3,8-dibromo-1,10-phenanthroline as monomers, ensuring the uniform coordination of N with Fe element in network. Then, the resulting FeN-CMP was treated by pyrolysis without structural collapse to obtain porous Fe N C electrocatalyst for ORR. The most active catalyst was fabricated under 900 °C, which exhibits remarkable ORR activity in alkaline medium with half-wave potential of 0.796 V (18 mV and 105 mV positive deviation from the commercial Pt/C catalyst and post-doping catalyst), high selectivity with nearly 4e- transfer process and excellent methanol tolerance. Our study first developed porous Fe N C electrocatalysts derived from Fe, N -anchoring CMPs based on pre-functionalization of monomers, which exhibits great potential as an alternative to commercial Pt/C catalyst for ORR, and provides a feasible strategy of developing multi-atoms doping catalysts for energy storage and conversion as well as heterogeneous catalysis. [ABSTRACT FROM AUTHOR]

[Display omitted] Water environmental pollution especially caused by bacteria, viruses and other microorganisms always would accelerate the spread of infectious diseases and has been one of the issues highly concerned by the World Health Organization for a long time. The development of novel antibacterial materials with high activity for water cleanness was of great importance for public health and ecological sustainable development. In this work, we developed two really free-standing conjugated microprous polymers (CMPs) film with large size and processibility by a simple and convenient solid surface-assisted polymerization between bromo- and aryl-acetylene monomers. With the solid interfacial orientation from silica nanofibers, the resulting CMPs film exhibited nanotube-liked morphology with BET surface area of 379.5 m2 g−1 and 480.1 m2 g−1. The introduction of antibacterial isocyanurate and acetanilide group into polymer skeleton brings the resulting CMPs film intrinsically antimicrobial capability and durability. The growth of E. coli can be completely inhibited by the resulting CMPs film even after several cycles. Our work was suggested to provide a new route for rational design of CMPs film or membrane with antibacterial activity for water treatment and sterilization. [ABSTRACT FROM AUTHOR]

[Display omitted] • A multifunctional self-floating photothermal materials (CS-CMPsHM) were synthesized. • The CS-CMPsHM are capable of adsorption antibiotics by interfacial steam generation. • The improved adsorption was due to specific π-π electron-donor–acceptor interactions. • Wastewater purification was achieved in simulated and actual water samples. • The inhibitory effect of the collected water on plant growth was significantly reduced. Solar-driven interfacial evaporation (SDIE) technology holds the promise of purification and removal of organic pollutants from water samples. In this work, an efficient SDIE composed of multifunctional self-floating photothermal materials based on candle soot-coated conjugated microporous polymer hollow spheres (CS-CMPsHM) for treatment of tetracycline (TC) wastewater is reported. By depositing candle soot nanoparticles, CS-CMPsHM achieved excellent interfacial evaporation performance by extending the light absorption. Additionally, the π-π interaction between CMP's unique conjugated network and TC molecules and the well-developed porosity facilitates the capture of target contaminants. The synthesized CS-CMPsHM evaporator demonstrated remarkable properties, i.e., excellent photothermal performance (with superior photothermal conversion efficiency up to 94 % and evaporation rate of 1.55 kg m−2h−1 under one sun irradiation), extremely low wet thermal conductivity (0.075 W m-1K−1), reusability, superior salt resistance, stability, adsorption of pollutants and renewable performance. Furthermore, CS-CMPsHM remains its excellent purification performance from real water samples (the Yellow River) measured by a three-dimensional fluorescence spectrometer. The results of biological toxicity show that the purified water recovered by the SDIE method effectively reduced the phytotoxicity of TC. With its straightforward and scalable manufacturing process, our CS-CMPsHM demonstrates promising potential as advanced photothermal materials for the treatment of various pollutants using SDIE. [ABSTRACT FROM AUTHOR]

[Display omitted] The inevitable intermittency of solar illumination during the interfacial evaporation process can cause a reduction in the evaporation performance of solar evaporators. Here, we report the fabrication of a new solar-driven interfacial evaporator using MXene nanosheets as the photothermal layer, modifying them with conjugated microporous polymer hollow microspheres, and then compounding them with the phase change material, in this case, cetyl alcohol, to form a composite evaporator (CE) that can perform all-weather solar interfacial evaporation. By combining interfacial evaporation photothermal conversion with energy storage, the evaporator achieves an evaporation rate of 1.57 kg⋅m−2⋅h−1 at a light intensity of 1 kW⋅m−2 and 2.79 kg⋅m−2⋅h−1 at a light intensity of 2 kW⋅m−2. In addition, the evaporator attains an excellent solar evaporation efficiency of over 91% in both cases and even in salt water. In addition, interestingly, our CE exhibits excellent continuous evaporation ability, e.g., the mass of evaporated water was increased by 0.36 kg⋅m−2 at a light intensity of 2 kW⋅m−2 compared to the cavity evaporator without the phase change material (PCM) when solar light was turned off. These results could be attributed to the fact that the energy released by the incorporated phase change material allows the evaporator to maintain stable evaporation under conditions of insufficient or intermittent solar irradiation, potentially providing a new opportunity for addressing the intermittent problem of evaporation at the solar interface due to unstable light intensity, thus showing great potential for practical continuous desalination. [ABSTRACT FROM AUTHOR]

• Synthesis of RCMP@TD-HA with HGM and CMP composite PCM. • RCMP@TD-HA has good light absorption and energy storage capacity. • The RCMP@TD-HA can continue to evaporate after the light source is dimmed. • O-RCMP@TD-HA achieves a 90% evaporation efficiency in oily water. Interfacial evaporation technology powered by solar energy is a clean and efficient solution for various scenarios, including seawater desalination, wastewater treatment, and sterilization. However, the intermittent nature of sunlight remains a challenge that must be overcome. In this study, a novel solar interfacial evaporator (CE) was prepared by mixing reduced graphene oxide (RGO) with conjugated microporous polymer hollow spheres (CMP-H) containing the phase change material tetradecanol (TD) and made into a coating, which was coated on an aerogel made of hollow glass microspheres (HGM). The evaporator has an evaporation rate of 1.68 kg·m−2·h−1 at 1 sun irradiation. In addition, our CE demonstrated exceptional continuous evaporation capabilities. For instance, after exposing the CE to two solar intensities for one hour and then turning off, the mass of evaporated water in our CE increased by 0.76 kg·m−2 compared to the CE without phase change material (PCM) until the surface temperature of the CE returned to its initial temperature. Furthermore, to enhance its versatility, the material has been modified to be oleophobic. The modified evaporator material was immersed in oil for 10 min. It was then evaporated in both oily water, achieving an evaporation rate of 1.62 kg·m−2·h−1 at 1 sun irradiation. These distinctive characteristics of our CE not only offer a novel solution to the constraints of the solar interfacial evaporation process caused by the intermittent nature of sunlight but also facilitate the efficient evaporation of oily wastewater, thus expanding the range of solar interfacial evaporation applications. [ABSTRACT FROM AUTHOR]