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Many porous organic polymers (POPs) possess excellent light absorption capacity and CO2 absorption performance owing to their conjugated skeletons and large specific surface area values. Some of these fascinating materials have inherent reaction sites for CO2 conversion and appropriate band structures to catalyze the CO2 reduction reaction. Therefore, these POPs have been used as heterogeneous catalysts in the photocatalytic CO2 reduction reaction. Among those POPs, four kinds of catalytic systems have been developed for realizing the CO2 photoreduction reaction: POPs loaded with noble metals, POPs loaded with non‐noble metals, POPs combined with inorganic semiconductors, and metal‐free POPs. Each of these catalytic systems has its own advantages and drawbacks. In general, the catalytic system of supported metals has higher catalytic efficiency but lower durability than metal‐free POPs. It should be noted that in the process of catalyst development, the co‐catalyst is gradually minimizing in POPs to achieve a more green CO2 photoreduction reaction. In this review, different types of POPs and the relationship between their structures and catalytic performance in the photocatalytic reduction of CO2 are summarized.

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Porous permeable films materials have very broad prospects in the treatment of sludge-containing waste water due to their large surface area and good microfiltration. In this work, highly ordered porous membranes have been prepared successfully on ice substrates using a poly(phenylene oxide) (BPPO)-SiO2 nanoparticle (NP) mixture by the breath figure method. Based on the theory of Pickering emulsion system and capillary flow, particle assisted membrane formation was analyzed. Another two sorts of new membranes SiO2/C membrane and hierarchical porous polymer (HPP) membrane, which were obtained by modification of the BPPO-SiO2 membrane by calcination and etching, were set up in a further study. Their properties were investigated through the methods of scanning electron microscopy (SEM), fourier transform infrared spectrometry (FTIR), ultraviolet spectrum (UV), capillary electrophoresis (CE), contact angle, and water flux tests. All these results demonstrate that both surface hydrophilicity and fouling resistance of the membrane would be improved by using SiO2 as a filler. The membranes with high permeability and antifouling properties were used for microfiltration applications.

Covalent organic frameworks (COFs) are a type of crystalline porous polymers that possess ordered structures and eternal pores. Because of their unique structural characteristics and diverse functional groups, COFs have been used in various application fields, such as adsorption, catalysis, separation, ion conduction, and energy storage. Among COFs, the fluorine‐containing COFs (fCOFs) have been developed for special applications by virtue of special physical and chemical properties resulting from fluorine element, which is a nonmetallic halogen element and possesses strong electronegativity. In the organic chemistry field, introducing fluorine into chemicals enables those chemicals to exhibit many interesting properties, and fluorine chemistry increasingly plays an important role in the history of chemical development. The introduction of fluorine in COFs can enhance the crystallinity, porosity, and stability of COFs, making COFs having superior performances and some new applications. In this review, the synthesis and application of fCOFs are systematically summarized. The application involves photocatalytic production of hydrogen peroxide, photocatalytic water splitting, electrocatalytic CO2 reduction, adsorption for different substances (H2, pesticides, per‐/polyfluoroalkyl substances, polybrominated diphenyl ethers, bisphenols, and positively charged organic dye molecules), oil−water separation, energy storage (e.g., zinc‐ion batteries, lithium−sulfur batteries), and proton conduction. Perspectives of remaining challenges and possible directions for fCOFs are also discussed.

In this work, a three-dimensional mathematical model including the fluid flow, heat transfer, mass transfer, and charge transfer incorporating electrochemical reactions was developed and applied to investigate the transport phenomena and performance in high-temperature proton exchange membrane fuel cells (HT-PEMFCs) with a membrane phosphoric acid doping level of 5, 7, 9, 11. The cell performance is evaluated and compared in terms of the polarization curve. The distributions of temperature, oxygen mass fraction, water mass fraction, proton conductivity, and local current density of four cases are given and compared in detail. Results show that the overall performance and local transport characteristics are significantly affected by the membrane phosphoric acid doping level.

Crystal phase structure of bimetallic alloy is an important factor determining the electrocatalytic activity toward oxidation of energy molecules. In this paper, PdCu bimetallic NPs with similar element composition and different crystal phase structural features have been synthesized hydrothermally by adjusting the content of ethylenediaminetetraacetic acid disodium salt (EDTA-2Na). Multiphase PdCu NPs composed of pure Pd and alloy phase are obtained with a low concentration (even as low as zero) of EDTA-2Na in synthetic systems while homogeneous PdCu alloy NPs are formed in the presence of EDTA-2Na with a high concentration. The catalytic activity of ethanol electrooxidation is increased from 3.1 mA·cm–2 of pure Pd NPs, to 3.6 mA·cm–2 of multiphase PdCu NPs, and to 5.0 mA·cm–2 of homogeneous PdCu alloy NPs (about 2360 mA mgPd –1). The surface composition and structural stability of homogeneous PdCu NPs were much less damaged during electrochemical measurements. Based on the experimental data, the formation mechanism of multiphase and homogeneous PdCu NPs and their structure–property relationship have been discussed.

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