Formic acid is a liquid, safe, and energy-dense carrier for fuel cells. Above all, it can be sustainably produced from the electroreduction of CO2. The formic acid market is currently saturated, and it requires alternative applications to justify additional production capacity. Fuel cell technologies offer a chance to expand it, while creating an opportunity for sustainability in the energy sector. Formic acid-based fuel cells represent a promising energy supply system in terms of high theoretical open-circuit voltage (1.48 V). Compared to common fuel cells running on H2 (e.g., proton-exchange membrane fuel cells), formic acid has a lower storage cost and is safer. This review focuses on the sustainable production of formic acid from CO2 and on the detailed analysis of commercial examples of formic acid-based fuel cells, in particular direct formic acid fuel cell stacks. Designs described in the literature are mostly at the laboratory scale, still, with 301 W as the maximum power output achieved. These case studies are fundamental for the scale-up; however, additional efforts are required to solve crossover and increase performance.

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Water scarcity threatens more and more people in the world. Moisture adsorption from the atmosphere represents a promising avenue to provide fresh water. Nanoporous sponges ("NPSs" ), new carbon-based sorbents synthesized from the pyrolysis of resorcinol-formaldehyde resin, can achieve comparable performance to metal organic framework-based systems, but at a significantly lower cost. Oxygen and nitrogen functionalities can be added to the NPS surface, through oxidation and addition of phenanthroline to the initial reagent mixture, respectively. The resulting NPS sorbents have high specific surface areas of 347 to 527 m 2 •g −1 and an average capillary-condensation-compatible pore size of 1.5 nm. When oxidized, the NPS can capture up to 0.28 g of water per gram of adsorbent at a relative pressure of 0.90 (0.14 g•g −1 at P/P sat = 0.40) and maintain this adsorption capacity over multiple adsorption/desorption cycles. Scaled-up synthesis of the NPS was performed and tested in an experimental water capture setup, showing good agreement between small-and larger-scale adsorption properties. Water adsorption isotherms fitted with the theoretical model proposed by Do and Do demonstrate that hydroxyl functionalities are of key importance to NPS behavior.

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