Continuous Modulation of Electrocatalytic Oxygen Reduction Activities of Single‐Atom Catalysts through<i>p‐n</i>Junction Rectification

Abstract

Fine-tuning single-atom catalysts (SACs) to surpass their activity limit remains challenging at their atomic scale. Herein, we exploit p-type semiconducting character of SACs having a metal center coordinated to nitrogen donors (MeN_x ) and rectify their local charge density by an n-type semiconductor support. With iron phthalocyanine (FePc) as a model SAC, introducing an n-type gallium monosulfide that features a low work function generates a space-charged region across the junction interface, and causes distortion of the FeN₄ moiety and spin-state transition in the Fe^II center. This catalyst shows an over two-fold higher specific oxygen-reduction activity than that of pristine FePc. We further employ three other n-type metal chalcogenides of varying work function as supports, and discover a linear correlation between the activities of the supported FeN₄ and the rectification degrees, which clearly indicates that SACs can be continuously tuned by this rectification strategy.