Optical Spectroscopic Determination of Photoexcited Small-Polaron Hopping in Transition Metal Oxide Photocatalysts

Abstract

Ultrafast small‐polaron formation profoundly shapes the electronic and catalytic behaviour of transition metal oxides (TMOs). Despite its significance, spectroscopic investigations of photoexcited polaron hopping in TMOs have been scarcely explored. Here, we present the first optical spectroscopic observation of photoexcited small-polaron hopping across the first-row TMOs, using femtosecond transient absorption spectroscopy. This polaronic feature rises within 500 fs as Drude‐type absorption converts to localized, polaronic absorption. Fitting with a small‐polaron optical conductivity model yields polaron relaxation energies of 400-650 meV, evidencing substantial energy loss upon self‐trapping. Kinetic analysis shows that oxides with open d-shells localize charge most readily: polaron formation activation barriers are low in all TMOs (0-10 meV), whereas hopping barriers remain much higher (200-350 meV). This work establishes key spectroscopic and kinetic insights, highlighting the trade-off between charge localization and mobility, as well as the critical role of polaron formation in TMOs photocatalysts.