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Nickel Incorporation into Fresh Iron Sulfide Precipitates Modulates Selectivity in Nitrite, Carbon Dioxide, and Proton Reduction
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DOI：10.1021/acs.inorgchem.5c03810.png)
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Abstract
En 中文
Nickel and iron sulfide minerals are ubiquitous in natural environments and are central to Earth's biogeochemical cycles. Both metals are found in metalloenzyme active sites that catalyze key redox reactions and have been proposed as protocatalysts in prebiotic chemistry. Here, we investigate how coprecipitated Ni-Fe sulfides differ in their ability to catalyze and directly reduce CO2, NO2 -, and protons and how these differences relate to their structural and compositional properties. Sulfides were synthesized by direct precipitation and characterized by X-ray absorption spectroscopy (XAS) at the Ni and Fe K-edges. At low Ni2+:Fe2+ ratios, nickel substitutionally incorporates into mackinawite (FeS m ) to form [Ni n Fe m ]S x phases, while high Ni2+ concentrations suppress FeS formation and favor NiS2-like structures. Increasing Ni content enhances the CO2 and proton reduction as well as direct NO2 - reduction, whereas Fe-rich samples favor NO2 - reduction by Fe2+ while suppressing H2 evolution. These contrasting behaviors indicate distinct mechanisms for proton, CO2, and nitrite reduction. The observed reactivity trends mirror biological metal utilization, where nickel catalyzes CO2 fixation and hydrogen evolution, underscoring the potential role of mixed Ni-Fe sulfides as protoenzymatic catalysts in early metabolic networks.
Keywords:
CRYSTAL-STRUCTURE REFINEMENT
AQUEOUS-SOLUTIONS
SODIUM-BOROHYDRIDE
AMINO-ACIDS
MACKINAWITE
HYDROGEN
PYRITE
NITROGENASE
COPRECIPITATION
ADSORPTION
Journal
IF:
4.7
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4.9W
Citations:
10.5W