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We report the use of fluorinated polymer zwitterions to build hybrid systems for efficient CO₂electroreduction. 

We report the hydrophobicity-enhanced reactivity of Cu²⁺ions as an ester hydrolase. 

We report the use of polymer N -heterocyclic carbenes (NHCs) to control the microenvironment surrounding metal nanocatalysts, thereby enhancing their catalytic performance in CO 2 electroreduction. Three polymer NHC ligands were designed with different hydrophobicity: hydrophilic poly(ethylene oxide) (PEO–NHC), hydrophobic polystyrene (PS–NHC), and amphiphilic block copolymer (BCP) (PEO- b -PS–NHC). All three polymer NHCs exhibited enhanced reactivity of gold nanoparticles (AuNPs) during CO 2 electroreduction by suppressing proton reduction. Notably, the incorporation of hydrophobic PS segments in both PS–NHC and PEO- b -PS–NHC led to a twofold increase in the partial current density for CO formation, as compared to the hydrophilic PEO–NHC. While polymer ligands did not hinder ion diffusion, their hydrophobicity altered the localized hydrogen bonding structures of water. This was confirmed experimentally and theoretically through attenuated total reflectance surface-enhanced infrared absorption spectroscopy and molecular dynamics simulation, demonstrating improved CO 2 diffusion and subsequent reduction in the presence of hydrophobic polymers. Furthermore, NHCs exhibited reasonable stability under reductive conditions, preserving the structural integrity of AuNPs, unlike thiol-ended polymers. The combination of NHC binding motifs with hydrophobic polymers provides valuable insights into controlling the microenvironment of metal nanocatalysts, offering a bioinspired strategy for the design of artificial metalloenzymes. 

Given the continuous and excessive CO 2 emission into the atmosphere from anthropomorphic activities, there is now a growing demand for negative carbon emission technologies, which requires efficient capture and conversion of CO 2 to value-added chemicals. This review highlights recent advances in CO 2 capture and conversion chemistry and processes. It first summarizes various adsorbent materials that have been developed for CO 2 capture, including hydroxide-, amine-, and metal organic framework-based adsorbents. It then reviews recent efforts devoted to two types of CO 2 conversion reaction: thermochemical CO 2 hydrogenation and electrochemical CO 2 reduction. While thermal hydrogenation reactions are often accomplished in the presence of H 2 , electrochemical reactions are realized by direct use of electricity that can be renewably generated from solar and wind power. The key to the success of these reactions is to develop efficient catalysts and to rationally engineer the catalyst–electrolyte interfaces. The review further covers recent studies in integrating CO 2 capture and conversion processes so that energy efficiency for the overall CO 2 capture and conversion can be optimized. Lastly, the review briefs some new approaches and future directions of coupling direct air capture and CO 2 conversion technologies as solutions to negative carbon emission and energy sustainability. 

Abstract We report the synthesis of ordered mesoporous ceria ( m CeO 2 ) with highly crystallinity and thermal stability using hybrid polymer templates consisting of organosilanes. Those organosilane-containing polymers can convert into silica-like nanostructures that further serve as thermally stable and mechanically strong templates to prevent the collapse of mesoporous frameworks during thermal-induced crystallization. Using a simple evaporation-induced self-assembly process, control of the interaction between templates and metal precursors allows the co-self-assembly of polymer micelles and Ce 3+ ions to form uniform porous structures. The porosity is well-retained after calcination up to 900 °C. After the thermal engineering at 700 °C for 12 h ( m CeO 2 -700-12 h), m CeO 2 still has a specific surface area of 96 m 2 g −1 with a pore size of 14 nm. m CeO 2 is demonstrated to be active for electrochemical oxidation of sulfite. m CeO 2 -700-12 h with a perfect balance of crystallinity and porosity shows the fastest intrinsic activity that is about 84 times more active than bulk CeO 2 and 5 times more active than m CeO 2 that has a lower crystallinity. 

New types of functional material structures will emerge if the shape and properties are controlled in three-dimensional nanodevices. Possible applications of these would be nanoelectronics and medical systems. Magnetic nanoparticles (MNPs) are especially important in electronics such as magnetic storage, sensors, and spintronics. Also, in those that are used as magnetic resonance imaging contrasts, and tissue specific therapeutic agents, as well as in the labeling and sorting of cells, drug delivery, separation of biochemical products, and in other medical applications. Most of these applications require MNPs to be chemically stable, uniform in size, and controllable in terms of their magnetic properties and shape. In this paper three new functions of iron (Fe)-based nanoparticles are reported: shape transformation, oxidation prevention, and self-alignment. The shape of the Fe nanoparticles could be controlled by changing their oxidation states and properties by using a nanocarbon coating. Full field X-ray microscopy using synchrotron radiation revealed controllable magnetic properties of MNPs at the L 3 edge which depended on the oxidation states. Then, inkjet printing was successfully performed to deposit a uniform layer of MNPs by the size.