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Abstract Heterogeneous photocatalysis combines the benefits of light‐mediated chemistry with that of a catalytic platform that facilitates re‐use of (often expensive) photocatalysts. This provides significant opportunities towards more economical, sustainable, safe, and user‐friendly chemical syntheses of both small and macromolecular compounds. This contribution outlines recent developments in the design of heterogenous photocatalysts and their use to mediate polymerizations. We outline four classes of heterogeneous photocatalysts in detail: Nanoparticles, conjugated and non‐conjugated polymer networks, metal‐organic frameworks (MOFs), and functionalized solid supports. 

This article describes the development of polymer brush-based heterogeneous photocatalysts for PET-RAFT polymerization in aqueous environments. 

Understanding multi-component transport through polymer membranes is critical for separation applications such as water purification, energy devices, etc. Specifically for CO2 reduction cells, where the CO2 reduction products (alcohols and carboxylate salts), crossover of these species is undesirable and improving the design of ion exchange membranes to prevent this behavior is needed. Previously, it was observed that acetate transport increased in copermeation with alcohols for cation exchange membranes consisting of poly(ethylene glycol) diacrylate (PEGDA) and 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and that the inclusion of poly(ethylene glycol) methacrylate (PEGMA) (n = 5, n represents the number of ethylene oxide repeat units) could suppress this behavior. Here, we further investigate the role of PEGMA in modulating fractional free volume and transport behavior of alcohols and carboxylates. PEGDA-PEGMA membranes of varied membranes are fabricated with both varied pre −polymerization water content at constant PEGMA (n = 9) content and varied PEGMA content at two pre −polymerization water contents (20 and 60 wt.% water). Permeability to sodium acetate also decreases in these charge-neutral PEGDA-PEGMA membranes compared to PEGMA-free films. Therefore, incorporation of comonomers such as PEGMA with long side chains may provide a useful membrane chemistry structural motif for preventing undesirable carboxylate crossover in polymer membranes.