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Metal-organic frameworks (MOFs) have been examined extensively for CO2 capture, and the influence of water co-adsorption on these processes is particularly relevant, as CO2 capture generally occurs in humid gas streams. To investi-gate CO2/H2O co-adsorption, binary adsorption isotherms of CO2 and H2O were measured on MOF-808-TFA (TFA = trifluoro-acetic acid). When water was pre-adsorbed on MOF-808-TFA, and a subsequent CO2 adsorption isotherm was measured, the CO2 adsorption was slightly reduced, as expected. However, when CO2 was adsorbed first and then an H2O adsorption iso-therm was measured, no significant H2O adsorption capacity was observed. The near complete loss of water adsorption ca-pacity was observed even when only a trace amount of CO2 was pre-adsorbed. The results show that unexpected, non-state function adsorption equilibria can result from dynamic MOF behaviors and defect sites, which may lead to counterintuitive adsorption data compared to traditional materials. 

Abstract Electrosynthesis, a viable path to decarbonize the chemical industry, has been harnessed to generate valuable chemicals under ambient conditions. Here, we present a membrane-free flow electrolyzer for paired electrocatalytic upcycling of nitrate (NO₃⁻) and chloride (Cl⁻) to ammonia (NH₃) and chlorine (Cl₂) gases by utilizing waste streams as substitutes for traditional electrolytes. The electrolyzer concurrently couples electrosynthesis and gaseous-product separation, which minimizes the undesired redox reaction between NH₃and Cl₂and thus prevents products loss. Using a three-stacked-modules electrolyzer system, we efficiently processed a reverse osmosis retentate waste stream. This yielded high concentrations of (NH₄)₂SO₄(83.8 mM) and NaClO (243.4 mM) at an electrical cost of 7.1 kWh per kilogram of solid products, while residual NH₃/NH₄⁺(0.3 mM), NO₂⁻(0.2 mM), and Cl₂/HClO/ClO⁻(0.1 mM) pollutants in the waste stream could meet the wastewater discharge regulations for nitrogen- and chlorine-species. This study underscores the value of pairing appropriate half-reactions, utilizing waste streams to replace traditional electrolytes, and merging product synthesis with separation to refine electrosynthesis platforms. 

Ever since the discovery of the charge density wave (CDW) transition in the kagome metal ${\mathrm{CsV}}_3{\mathrm{Sb}}_5$, the nature of its symmetry breaking has been under intense debate. While evidence suggests that the rotational symmetry is already broken at the CDW transition temperature ( $T_{\mathrm{CDW}}$), an additional electronic nematic instability well below $T_{\mathrm{CDW}}$has been reported based on the diverging elastoresistivity coefficient in the anisotropic channel ( $m_{E_{2g}}$). Verifying the existence of a nematic transition below $T_{\mathrm{CDW}}$is not only critical for establishing the correct description of the CDW order parameter, but also important for understanding low-temperature superconductivity. Here, we report elastoresistivity measurements of ${\mathrm{CsV}}_3{\mathrm{Sb}}_5$using three different techniques probing both isotropic and anisotropic symmetry channels. Contrary to previous reports, we find the anisotropic elastoresistivity coefficient $m_{E_{2g}}$is temperature independent, except for a step jump at $T_{\mathrm{CDW}}$. The absence of nematic fluctuations is further substantiated by measurements of the elastocaloric effect, which show no enhancement associated with nematic susceptibility. On the other hand, the symmetric elastoresistivity coefficient $m_{A_{1g}}$increases below $T_{\mathrm{CDW}}$, reaching a peak value of 90 at $T^{*}=20\mathrm{K}$. Our results strongly indicate that the phase transition at $T^{*}$is not nematic in nature and the previously reported diverging elastoresistivity is due to the contamination from the $A_{1g}$channel. Published by the American Physical Society2024