氧还原反应
电子传输链
自旋(空气动力学)
还原(数学)
电子
氧气
凝聚态物理
化学物理
物理
化学
核物理学
量子力学
电化学
生物化学
几何学
数学
电极
热力学
作者
Priscila Vensaus,Yunchang Liang,Jean‐Philippe Ansermet,Jonas Fransson,Magalı́ Lingenfelder
标识
DOI:10.26434/chemrxiv-2025-xvbgs
摘要
Oxygen evolution (OER) and oxygen reduction (ORR) reactions are central to the efficiency of electrolysis and fuel cells, involving the paramagnetic triplet ground state of oxygen and the singlet ground state of water. Here, we demonstrate that spin-polarized currents enhance the ORR activity. Using a silver-coated nickel electrode over a neodymium (Nd) magnet, we observed that ORR performance is maximized when the Ag layer is thinner than the spin diffusion length of silver—conditions under which spin alignment at the electrode–electrolyte interface is maintained. In contrast, thicker Ag layers lead to spin relaxation and diminished electrocatalytic activity. A model description of this system shows that a very weakly spin-polarized injected current leads to a substantial spin-polarization at the interface, indicating that the simultaneous transfer of two-electrons can provide the necessary electrons while maintaining the conservation of the angular momentum during ORR. These findings highlight the critical role of spin-selective charge transfer and offer new insights into the control of reaction pathways in oxygen electrocatalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI