Photoreduction of inorganic carbon(+IV) by elemental sulfur: Implications for prebiotic synthesis in terrestrial hot springs.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33208363.
- Also identified by DOI 10.1126/sciadv.abc3687 and PMC identifier 7673799.
- Licence recorded as CC BY-NC.
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Abstract
Terrestrial hydrothermal systems have been proposed as alternative birthplaces for early life but lacked reasonable scenarios for the supply of biomolecules. Here, we show that elemental sulfur (S<sup>0</sup>), as the dominant mineral in terrestrial hot springs, can reduce carbon dioxide (CO<sub>2</sub>) into formic acid (HCOOH) under ultraviolet (UV) light below 280 nm. The semiconducting S<sup>0</sup> is indicated to have a direct bandgap of 4.4 eV. The UV-excited S<sup>0</sup> produces photoelectrons with a highly negative potential of -2.34 V (versus NHE, pH 7), which could reduce CO<sub>2</sub> after accepting electrons from electron donors such as reducing sulfur species. Simultaneously, UV light breaks sulfur bonds, benefiting the adsorption of charged carbonates onto S<sup>0</sup> and assisting their photoreduction. Assuming that terrestrial hot springs covered 1% of primitive Earth's surface, S<sup>0</sup> at 10 μM could have produced maximal 10<sup>9</sup> kg/year HCOOH within 10-cm-thick photic zones, underlying its remarkable contributions to the accumulation of prebiotic biomolecules.