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The development of effective CO2 sorbents is vital to achieving net-zero CO2 emission targets. MgO promoted with molten salts is an emerging class of CO2 sorbents. However, the structural features that govern their performance remain elusive. Using in situ time-resolved powder x-ray diffraction, we follow the structural dynamics of a model NaNO3-promoted, MgO-based CO2 sorbent. During the first few cycles of CO2 capture and release, the sorbent deactivates owing to an increase in the sizes of the MgO crystallites, reducing in turn the abundance of available nucleation points, i.e., MgO surface defects, for MgCO3 growth. After the third cycle, the sorbent shows a continuous reactivation, which is linked to the in situ formation of Na2Mg(CO3)2 crystallites that act effectively as seeds for MgCO3 nucleation and growth. Na2Mg(CO3)2 forms due to the partial decomposition of NaNO3 during regeneration at T ≥ 450°C followed by carbonation in CO2. ISSN:2375-2548

Open data for publication "Probing the dynamics of the local structure of Na in NaNO3-promoted, MgO-based CO2 sorbents via X-ray absorption spectroscopy "

The influence of the phase of the ZrO2 support (monoclinic, tetragonal, and amorphous, referred to as m-, t-, and am-, respectively) on the nature of the surface species involved in methanol synthesis and the rates of their formation on ZrO2-supported, In-based catalysts for CO2 hydrogenation has been investigated. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) at 300 degrees C and 20 bar (H-2:CO2:N-2 = 3:1:1 volume ratio) on m-ZrO2:In, In2O3/t-ZrO2, and In2O3/am-ZrO2 catalysts (m-ZrO2:In is a solid solution) shows that formate species (HCOO*) appear prior to methoxy species (*OCH3), and both intermediates form faster on the more active m- ZrO2:In catalyst. Only formate bands are detected for the In2O3/t-ZrO2 catalyst. For these materials, indium sites are essential for the formation of HCOO* and *OCH3 species as only carbonate species are observed on m-, t-, and am-ZrO2 supports under CO2 hydrogenation conditions. The nature of the reaction intermediates is confirmed by ex situ solid-state nuclear magnetic resonance (NMR), where both methoxy and formate species are detected in m-ZrO2:In and In2O3/am-ZrO2, respectively, but only a weak formate peak is observed for In2O3/t-ZrO2. The presence of a major methoxy peak and only a very minor formate signal in unsupported In2O3 indicates that an india-zirconia interface is required for the effective stabilization of formate species. Catalytic tests in a fixed bed reactor are consistent with both CO and Me0H being primary products of CO2 hydrogenation; the tests also show that the methanol selectivity and space time yield decrease in the following order: m-ZrO2:In > In2O3/t-ZrO2 > In2O3/am-ZrO2 for all of the contact times tested. ISSN:1932-7455 ISSN:1932-7447

MgO-based CO2 sorbents promoted with molten alkali metal nitrates (e.g., NaNO3) have emerged as promising materials for CO2 capture and storage technologies due to their low cost and high theoretical CO2 uptake capacities. Yet, the mechanism by which molten alkali metal nitrates promote the carbonation of MgO (CO2 capture reaction) remains debated and poorly understood. Here, we utilize O-18 isotope labeling experiments to provide new insights into the carbonation mechanism of NaNO3-promoted MgO sorbents, a system in which the promoter is molten under operation conditions and hence inherently challenging to characterize. To conduct the O-18 isotope labeling experiments, we report a facile and large-scale synthesis procedure to obtain labeled MgO with a high O-18 isotope content. We use Raman spectroscopy and in situ thermogravimetric analysis in combination with mass spectrometry to track the O-18 label in the solid (MgCO3), molten (NaNO3), and gas (CO2) phases during the CO2 capture (carbonation) and regeneration (decarbonation) reactions. We discovered a rapid oxygen exchange between CO2 and MgO through the reversible formation of surface carbonates, independent of the presence of the promoter NaNO3. On the other hand, no oxygen exchange was observed between NaNO3 and CO2 or NaNO3 and MgO. Combining the results of the O-18 labeling experiments, with insights gained from atomistic calculations, we propose a carbonation mechanism that, in the first stage, proceeds through a fast, surface-limited carbonation of MgO. These surface carbonates are subsequently dissolved as [Mg2+center dot center dot center dot CO32-] ionic pairs in the molten NaNO3 promoter. Upon reaching the solubility limit, MgCO3 crystallizes at the MgO/NaNO3 interface., JACS Au, 2 (12), ISSN:2691-3704

The thermal carburization of MoO3 nanobelts (nb) and SiO2-supported MoO3 nanosheets under a 1 : 4 mixture of CH4 : H-2 yields Mo2C-nb and Mo2C/SiO2. Following this process by in situ Mo K-edge X-ray absorption spectroscopy (XAS) reveals different carburization pathways for unsupported and supported MoO3. In particular, the carburization of alpha-MoO3-nb proceeds via MoO2, and that of MoO3/SiO(2)via the formation of highly dispersed MoOx species. Both Mo2C-nb and Mo2C/SiO2 catalyze the dry reforming of methane (DRM, 800 degrees C, 8 bar) but their catalytic stability differs. Mo2C-nb shows a stable performance when using a CH4-rich feed (CH4 : CO2 = 4 : 2), however deactivation due to the formation of MoO2 occurs for higher CO2 concentrations (CH4 : CO2 = 4 : 3). In contrast, Mo2C/SiO2 is notably more stable than Mo2C-nb under the CH4 : CO2 = 4 : 3 feed. The influence of the morphology of Mo2C and its dispersion on silica on the structural evolution of the catalysts under DRM is further studied by in situ Mo K-edge XAS. It is found that Mo2C/SiO2 features a higher resistance to oxidation under DRM than the highly crystalline unsupported Mo2C-nb and this correlates with an improved catalytic stability. Lastly, the oxidation of Mo in both Mo2C-nb and Mo2C/SiO2 under DRM conditions in the in situ XAS experiments leads to an increased activity of the competing reverse water gas shift reaction., Catalysis Science & Technology, 12 (18), ISSN:2044-4753, ISSN:2044-4761

SGK/SSCr Newsletter, 108, ISSN:0021-8898, ISSN:1662-534X, ISSN:1662-5358, Annual meeting 2022

Chemical looping is an emerging technology to produce high purity hydrogen from fossil fuels or biomass with the simultaneous capture of the CO2 produced at the distributed scale. This process requires the availability of stable Fe2O3-based oxygen carriers. Fe2O3–Al2O3 based oxygen carriers exhibit a decay in the H2 yield with cycle number, due to the formation of FeAl2O4 that possesses a very low capacity for water splitting at typical operating conditions of conventional chemical looping schemes (700–1000 °C). In this study, the addition of sodium (via a sodium salt) in the synthesis of Fe2O3–Al2O3 oxygen carriers was assessed as a means to counteract the cyclic deactivation of the oxygen carrier. Detailed insight into the oxygen carrier's structure was gained by combined X-ray powder diffraction (XRD), X-ray absorption spectroscopy (XAS) at the Al, Na and Fe K-edges and scanning transmission electron microscopy/energy-dispersive X-ray spectroscopy (STEM/EDX) analyses. The addition of sodium prevented the formation of FeAl2O4 and stabilized the oxygen carrier via the formation of a layered structure, Na-β-Al2O3 phase. The material, i.e. Na-β-Al2O3 stabilized Fe2O3, showed a stable H2 yield of ca. 13.3 mmol g−1 over 15 cycles., Journal of Materials Chemistry A, 10 (19), ISSN:2050-7488, ISSN:2050-7496

The addition of molten alkali metal salts drastically accelerates the kinetics of CO2 capture by MgO through the formation of MgCO3. However, the growth mechanism, the nature of MgCO3 formation, and the exact role of the molten alkali metal salts on the CO2 capture process remain elusive, holding back the development of more-effectiveMgO-based CO2 sorbents. Here, we unveil the growth mechanism of MgCO3 under practically relevant conditions using a well-defined, yet representative, model system that is a MgO(100) single crystal coated with NaNO3. The model system is interrogated by in situ X-ray reflectometry coupled with grazing incidence X-ray diffraction, scanning electron microscopy, and high-resolution transmission electron microscopy. When bare MgO(100) is exposed to a flow of CO2, a noncrystalline surface carbonate layer of ca. 7-Å thickness forms. In contrast, when MgO(100) is coated with NaNO3, MgCO3 crystals nucleate and grow. These crystals have a preferential orientation with respect to the MgO(100) substrate, and form at the interface between MgO(100) and the molten NaNO3. MgCO3 grows epitaxially with respect to MgO(100), and the lattice mismatch between MgCO3 and MgO is relaxed through lattice misfit dislocations. Pyramid-shaped pits on the surface ofMgO, in proximity to and below the MgCO3 crystals, point to the etching of surface MgO, providing dissolved [Mg2+ O2-] ionic pairs forMgCO3 growth. Our studies highlight the importance of combining X-rays and electron microscopy techniques to provide atomic to micrometer scale insight into the changes occurring at complex interfaces under reactive conditions., Proceedings of the National Academy of Sciences of the United States of America, 118 (26), ISSN:0027-8424, ISSN:1091-6490