RESUMEN
Understanding the mechanism of water oxidation to dioxygen represents the bottleneck towards the design of efficient energy storage schemes based on water splitting. The investigation of kinetic isotope effects has long been established for mechanistic studies of various such reactions. However, so far natural isotope abundance determination of O2 produced at solid electrode surfaces has not been applied. Here, we demonstrate that such measurements are possible. Moreover, they are experimentally simple and sufficiently accurate to observe significant effects. Our measured kinetic isotope effects depend strongly on the electrode material and on the applied electrode potential. They suggest that in the case of iron oxide as the electrode material, the oxygen evolution reaction occurs via a rate-determining O-O bond formation via nucleophilic water attack on a ferryl unit.
RESUMEN
Besides gas-water-exchange in surface waters, respiratory consumption of dissolved oxygen (DO) in adjacent riparian groundwater may trigger the addition of so far hardly explored sources from the unsaturated zone. These processes also systematically influence stable isotope ratios of DO and were investigated together with Cl- as a conservative tracer for water mixing in a near-river riparian groundwater system. The study focused on a losing stream section of the Selke River at the foot of the Harz Mountains (Germany). The study area exposed steep DO gradients between the stream water and riparian groundwater between April 2016 and May 2017. Our results indicated dominant influences of microbial community respiration with observed DO concentration gradients. These observations can be explained by DO from the river that is subject to fractionation by microbial respiration with a typical fractionation factor (αr) of 0.982. However, with such respiration dominance, we expected a simultaneous enrichment of δ18ODO towards values that are more positive than the well-known atmospheric O2 signal of +23.9 versus the Vienna Standard Mean Ocean Water standard (VSMOW). Surprisingly, our measurements revealed much lower δ18ODO values between +22 and +18 in the near-river groundwater. Mass balance calculations revealed that the DO pool in the shallow and unconfined aquifer receives contributions of up to about 80% by diffusion of oxygen from the vadose zone with a distinctly lower isotope value than the one of the atmosphere. This finding about additional oxygen sources from the unsaturated zone has numerous ramifications for oxygen related processes in near-river environments including the oxidation of pollutants, nutrients and ecosystem health.
