Electrochemical CO2 reduction (EC-CO2R) has seen a resurgence in interest over the past several years; however, the means of analyzing catalytically produced products continues to rely on decades-old methods such as gas chromatography, high-performance liquid chromatography, and nuclear magnetic resonance. Real-time analysis of the gaseous and liquid products of this reaction is highly desirable; however, few analytical techniques have been developed thus far to meet this need. Here, we demonstrate the first use of selected-ion flow-tube mass spectrometry (SIFT-MS) as an analytical tool capable of measuring in real time both the gas- and liquid-phase products of EC-CO2R in aqueous solution. SIFT-MS uses well-understood ion–molecule reactions to enable the analysis of similar multicomponent mixtures by preventing substantial fragmentation of the analyte. We lay out the framework in which to evaluate the tool's capabilities and show that the C1–C3 hydrocarbon, alcohol, and aldehyde products of CO2R should be quantitatively detectable.

Copper oxides have been of considerable interest as electrocatalysts for CO2 reduction (CO2R) in aqueous electrolytes. However, their role as an active catalyst in reducing the required overpotential and improving the selectivity of reaction compared with that of polycrystalline copper remains controversial. Here, we introduce the use of selected-ion flow tube mass spectrometry, in concert with chronopotentiometry, in situ Raman spectroscopy, and computational modeling, to investigate CO2R on Cu2O nanoneedles, Cu2O nanocrystals, and Cu2O nanoparticles. We show experimentally that the selective formation of gaseous C2 products (i.e., ethylene) in CO2R is preceded by the reduction of the copper oxide (Cu2OR) surface to metallic copper. On the basis of density functional theory modeling, CO2R products are not formed as long as Cu2O is present at the surface because Cu2OR is kinetically and energetically more favorable than CO2R.

Antiferromagnetic insulators are a ubiquitous class of magnetic materials, holding the promise of low-dissipation spin-based computing devices that can display ultra-fast switching and are robust against stray fields. However, their imperviousness to magnetic fields also makes them difficult to control in a reversible and scalable manner. Here we demonstrate a novel proof-of-principle ionic approach to control the spin reorientation (Morin) transition reversibly in the common antiferromagnetic insulator α-Fe₂O₃ (haematite) - now an emerging spintronic material that hosts topological antiferromagnetic spin-textures and long magnon-diffusion lengths. We use a low-temperature catalytic-spillover process involving the post-growth incorporation or removal of hydrogen from α-Fe₂O₃ thin films. Hydrogenation drives pronounced changes in its magnetic anisotropy, Néel vector orientation and canted magnetism via electron injection and local distortions. We explain these effects with a detailed magnetic anisotropy model and first-principles calculations. Tailoring our work for future applications, we demonstrate reversible control of the room-temperature spin-state by doping/expelling hydrogen in Rh-substituted α-Fe₂O₃.