This perspective proposes a potential pathway to diminish atmospheric CO2 accumulations which is distinct from traditional carbon capture and geological sequestration strategies and from existing negative emissions technologies (NETs). Unlike conventional sorbent- or solvent-based CO2 capture processes where substantial energy expenditures are associated with demixing and desorbing CO2, the single-step carbon sequestration and storage (sCS2) approach relies on electrolytic carbonate mineral precipitation using renewable energy within a simple and scalable process design. Although numerous approaches have implied electrolysis for carbon management, the sCS2 approach is unique in the following ways: (1) CO2 mineralization for promoting solid carbonate formation: The thermodynamic and kinetic barriers to carbonate precipitation are overcome by direct and in situ electrochemical forcing to stabilize dissolved inorganic carbon and divalent cations [Ca,Mg] to form carbonate minerals. (2) Flow-through membraneless electrolysis: A flowing electrolyte (seawater) is dissociated while in motion. The process utilizes cost-effective mesh electrodes while also decreasing the number of components and assembly steps and reducing the risk of device failure. (3) Integrated electrolytic reactor–rotary drum filter: An electroactive thin-film mesh cathode (eTFC) is suggested to be integrated within a rotary drum filter configuration, allowing for the filtration of dilute and polydispersed mineral precipitates at a low energy cost. These attributes render sCS2 as an approach worthy of more detailed evaluation, development, and scaling for global-scale carbon management.

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The Cl−-induced corrosion of metals and alloys is of relevance to a wide range of engineered materials, structures, and systems. Because of the challenges in studying pitting corrosion in a quantitative and statistically significant manner, its kinetics remain poorly understood. Herein, by direct, nano- to micro-scale observations using vertical scanning interferometry (VSI), we examine the temporal evolution of pitting corrosion on AISI 1045 carbon steel over large surface areas in Cl−-free, and Cl−-enriched solutions. Special focus is paid to examine the nucleation and growth of pits, and the associated formation of roughened regions on steel surfaces. By statistical analysis of hundreds of individual pits, three stages of pitting corrosion, namely, induction, propagation, and saturation, are quantitatively distinguished. By quantifying the kinetics of these processes, we contextualize our current understanding of electrochemical corrosion within a framework that considers spatial dynamics and morphology evolutions. In the presence of Cl− ions, corrosion is highly accelerated due to multiple autocatalytic factors including destabilization of protective surface oxide films and preservation of aggressive microenvironments within the pits, both of which promote continued pit nucleation and growth. These findings offer new insights into predicting and modeling steel corrosion processes in mid-pH aqueous environments.

Albite (NaAlSiO), a framework silicate of the plagioclase feldspar family and a common constituent of felsic rocks, is often present in the siliceous mineral aggregates that compose concrete. When exposed to radiation (e.g., in the form of neutrons) in nuclear power plants, the crystal structure of albite can undergo significant alterations. These alterations may degrade its chemical durability. Indeed, careful examinations of Ar-implanted albite carried out using Fourier transform infrared spectroscopy (FTIR) and molecular dynamics simulations show that albite's crystal structure, upon irradiation, undergoes progressive disordering, resulting in an expansion in its molar volume (i.e., a reduction of density) and a reduction in the connectivity of its atomic network. This loss of network connectivity (i.e., rigidity) results in an enhancement of the aqueous dissolution rate of albite-measured using vertical scanning interferometry (VSI) in alkaline environments-by a factor of 20. This enhancement in the dissolution rate (i.e., reduction in chemical durability) of albite following irradiation has significant impacts on the durability of felsic rocks and of concrete containing them upon their exposure to radiation in nuclear power plant (NPP) environments.