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Results for “redox”
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Substituent Impact on Quinoxaline Performance and Degradation in Redox Flow Batteries
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Development of the Squaramide Scaffold for High Potential and Multielectron Catholytes for Use in Redox Flow Batteries
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Metal–Metal Redox Exchange to Produce Heterometallic Manganese–Cobalt Oxo Cubanes via a “Dangler” Intermediate
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Surface-to-bulk redox coupling through thermally-driven Li redistribution in Li- and Mn-rich layered cathode materials
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Redox Cycling Driven Transformation of Layered Manganese Oxides to Tunnel Structures
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Scalable Synthesis of InAs Quantum Dots Mediated through Indium Redox Chemistry
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Effects of Covalency on Anionic Redox Chemistry in Semiquinoid-Based Metal-Organic Frameworks
Abstract not provided
Redox Dynamics of Active VO x Sites Promoted by TiO x during Oxidative Dehydrogenation of Ethanol Detected by Operando Quick XAS
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Linking Stream Chemistry to Subsurface Redox Architecture
As drinking-water scarcity grows worldwide, we need to improve predictions of the quantity and quality of our water resources. An overarching problem for model improvement is that we do not know the geological structure of aquifers in sufficient detail. In this work, we demonstrate that mineral-water reactions imprint structure in the subsurface that impacts the flow and transport of some chemical species. Specifically, pyrite, a ubiquitous mineral, commonly oxidizes and depletes in the upper layers of the weathering profile in most humid watersheds, only remaining at depths of meters. We hypothesize that variations in concentrations (C) of pyrite-derived sulfate released into rivers as a function of discharge (q) reflect the rate-limiting step and depth of pyrite-oxidizing layers. We found that log C - log q behaviors thus differ in small and large watersheds in the Susquehanna River Basin as well as in selected watersheds in the Western United States. Although coal mining changes pyrite oxidation from closed to open system with respect to O 2 , patterns in stream chemistry as a function of discharge are consistent with deep and shallow pyrite oxidation zones in small and large watersheds respectively. Therefore, understanding the subsurface patterns of mineral reactions and how they affect the architecture of aquifers will elucidate patterns of changing river chemistry and our ability to manage water resources in the future under accelerated land use and climate change.
Volatiles and Redox Along the East African Rift
Abstract The upper mantle under the Afar Depression in the East African Rift displays some of the slowest seismic wave speeds observed globally. Despite the extreme nature of the geophysical anomaly, lavas that erupted along the East African Rift record modest thermal anomalies. We present measurements of major elements, H 2 O, S, and CO 2 , and Fe 3+ /ΣFe and S 6+ /ΣS in submarine glasses from the Gulf of Aden seafloor spreading center and olivine‐, plagioclase‐, and pyroxene‐hosted melt inclusions from Erta Ale volcano in the Afar Depression. We combine these measurements with literature data to place constraints on the temperature, H 2 O, andfO 2 of the mantle sources of these lavas as well as the initial and final pressures of melting. The Afar mantle plume is C/FOZO/PHEM in isotopic composition, and we suggest that this mantle component is damp, with 852 ± 167 ppm H 2 O, not elevated infO 2 compared to the depleted MORB mantle, and has temperatures of ∼1401–1458°C. This is similar infO 2 and H 2 O to the estimates of C/FOZO/PHEM in other locations. Using the moderate H 2 O contents of the mantle together with the moderate thermal anomaly, we find that melting begins at around 93 km depth and ceases at around 63 km depth under the Afar Depression and at around 37 km depth under the Gulf of Aden, and that ∼1%–29% partial melts of the mantle can be generated under these conditions. We speculate that the presence of melt, and not elevated temperatures or high H 2 O contents, are the cause for the prominent geophysical anomaly observed in this region.
Coupling between oxygen redox and cation migration explains unusual electrochemistry in lithium-rich layered oxides
Abstract not provided
Anionic redox reaction in layered NaCr2/3Ti1/3S2 through electron holes formation and dimerization of S-S
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Negative cooperativity upon hydrogen bond-stabilized O2 adsorption in a redox-active metal–organic framework
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