In gas adsorption and metal recovery, inexpensive and covalently bonded porous polymers offer industrial feasibility, despite the challenge of having reactive functionalities while maintaining porosity. Herein, three highly porous covalent organic polymers (COPs), COP-210, COP-211, and COP-212, with porphyrin functionalities that are readily synthesized by a Friedel–Crafts reaction using chlorinated solvents as linkers are reported. The polymers exhibit competitive adsorption capacities for CO₂, H2, and CH4. Their porphyrin sites proved particularly effective in precious metal recovery, where COPs exhibit high selectivity toward gold, platinum, palladium, and silver. Analysis reveals that reductive metal capture is prevalent for gold and silver. Platinum is also captured through a combination of reduction and chelation. The gold adsorption capacities are 0.901–1.250 g g−1 with fast adsorption kinetics at low pH. COP-212 selectively recovers 95.6% of gold from actual electronic waste (e-waste) collected from junkyards. The results show that the inexpensive and scalable porous porphyrin polymers offer great potential in gas capture, separation, and precious metal recovery.

Cafer T. Yavuz received his PhD from Rice University in 2008 with a Welch scholarship under the supervision of Vicki Colvin. He then worked as a postdoctoral scholar at the University of California, Santa Barbara, with Galen Stucky. He started his independent group in 2010 at KAIST, Korea. He is currently a professor of chemistry at the King Abdullah University of Science and Technology in Saudi Arabia. His research focuses on the design and synthesis of nanoscale and porous materials for applications in energy and the environment. He uses fine chemistry in confined spaces to enable rapid and targeted transformations of CO₂, methane, and water.

Pyrazole-linked covalent organic polymer is synthesized using an asynchronous double Schiff base from readily available monomers. The one-pot reaction features no metals as a building block or reagent, hence facilitating the structural purity and industrial scalability of the design. Through a single-crystal study on a model compound, the double Schiff base formation is found to follow syn addition, a kinetically favored product, suggesting that reactivity of the amine and carbonyls dictate the order and geometry of the framework building. The highly porous pyrazole polymer COP-214 is chemically resistant in reactive conditions for over two weeks and thermally stable up to 425 °C in air. COP-214 shows well-pronounced gas capture and selectivities, and a high CO₂/N₂ selectivity of 102. The strongly coordinating pyrazole sites show rapid uptake and quantitative selectivity of Pd (II) over several coordinating metals (especially Pt (II)) at all pH points that are tested, a remarkably rare feature that is best explained by detailed analysis as the size-selective strong coordination of Pd onto pyrazoles. Density functional theory (DFT) calculations show energetically favorable Pd binding between the metal and N-sites of COP-214. The polymer is reusable multiple times without loss of activity, providing great incentives for an industrial prospect.

Formic acid is a compelling chemical storage platform for hydrogen gas, but the lack of an efficient dehydrogenation catalyst is preventing its commercial use. In this issue of Matter, Wang et al. report a fine-tuned zirconium metal-organic framework with palladium nanoparticles that effectively dehydrogenates formic acid without degradation.

Activated carbon has been used in a wide range of applications owing to its large specific area, facile synthesis, and low cost. The synthesis of activated carbon mostly relies on potassium hydroxide (KOH)-mediated activation which leads to the formation of micropores (<2 nm) after a washing step with acid. Here we report the preparation of activated carbon with an anomalously large surface area (3288 m2 g−1), obtained by employing an activation process mediated by cesium (Cs) ions. The high affinity of the carbon lattice for Cs ions induces immense interlayer expansion upon complexation of the intercalant Cs ion with the carbon host. Furthermore, the Cs-activation process maintains the nitrogen content of the carbon source by enabling the activation process at low temperature. The large surface area and well-preserved nitrogen content of Cs-activated carbon takes advantage of its enhanced interaction with CO₂ molecules (for superior CO₂ capture) and lithium ions (for improved Li ion storage), respectively. The present investigation unveils a new approach toward tuning the key structural properties of activated carbon; that is, controlling the affinity of the carbon host for the intercalant ion when they engage in complex formation during the activation process.