Spin-Selective Oxygen Evolution Reaction in Chiral Iron Oxide Nanoparticles: Synergistic Impact of Inherent Magnetic Moment and Chirality.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37737823.
- Also identified by DOI 10.1021/acs.nanolett.3c02752.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Electron spin polarization is identified as a promising avenue for enhancing the oxygen evolution reaction (OER), which is the bottleneck that limits the energy efficiency of water-splitting. Here, we report that both ferrimagnetic (f-Fe<sub>3</sub>O<sub>4</sub>) and superparamagnetic iron oxide (s-Fe<sub>3</sub>O<sub>4</sub>) catalysts can exhibit external magnetic field (Hext)-induced OER enhancement, and the activity is proportional to their intrinsic magnetic moment. Additionally, the chirality-induced spin selectivity (CISS) effect was utilized in synergy with Hext to get a maximum enhancement of up to 89% improvement in current density (at 1.8 V vs RHE) with a low onset potential of 270 mV in s-Fe<sub>3</sub>O<sub>4</sub> catalysts. Spin polarization and the resultant spin selectivity suppress the production of H<sub>2</sub>O<sub>2</sub> and promote the formation of ground state triplet O<sub>2</sub> during the OER. Furthermore, the design of chiral s-Fe<sub>3</sub>O<sub>4</sub> with synergistic spin potential effect demonstrates a high spin polarization of ∼42%, as measured using conductive atomic force microscopy (c-AFM).