The consequences of the evolution of the active site in the oxygen reduction reaction catalyzed by iron phthalocyanine (FePc) submonolayers deposited on the Ag(110) surface are explored. The capacity of reversibly and sharply switching the magnetic state of FePc molecules by chemical means is conclusively evidenced by X-ray magnetic circular dichroism (XMCD) at the Fe L<inf>2,3</inf> absorption edge. In the molecular oxygen-dosed phase, oxygen intercalates between the molecule and the surface, thereby switching the Fe magnetic moment from a nearly negligible (m<inf>Tot</inf><sup>exp</sup> ? 0.26(1) ?<inf>B</inf>) to an order of magnitude larger value (m<inf>Tot</inf><sup>exp</sup> ? 2.1(2) ?<inf>B</inf>). Moreover, the characteristic XMCD spectrum undergoes a crossover from metallic to oxidized Fe(III)-like line shape, in accordance with an oxygen-induced decoupling of the molecular electronic states from the underlying metal surface. The FePc acts as a reversible bifunctional chemical-magnetic switch at the atomic monolayer scale. (Chemical Equation Presented).
Reversible Fe Magnetic Moment Switching in Catalytic Oxygen Reduction Reaction of Fe-Phthalocyanine Adsorbed on Ag(110)
Forrer D;
2015
Abstract
The consequences of the evolution of the active site in the oxygen reduction reaction catalyzed by iron phthalocyanine (FePc) submonolayers deposited on the Ag(110) surface are explored. The capacity of reversibly and sharply switching the magnetic state of FePc molecules by chemical means is conclusively evidenced by X-ray magnetic circular dichroism (XMCD) at the Fe LI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
