Excess Activity Tuned by Distorted Tetrahedron in CoMoO 4 for Oxygen Evolution

Oxygen vacancies enable modulating surface reconstruction of transition metal oxides containing metal–oxygen polyhedrons into metallic oxyhydroxide for oxygen evolution reaction (OER), while revealing reconstructing mechanism is stuck by the requirement to precisely control exact sites of these vacancies. Herein, oxygen vacancies are localized only within MoO 4 tetrahedrons rather than CoO 6 octahedrons in CoMoO 4 catalyst, guaranteeing coherent reconstruction of CoO 6 octahedrons into pure CoOOH with tunable activities for OER. Meanwhile, distorted tetrahedron accelerates the dissolution of Mo atoms into alkaline electrolyte, triggering spontaneous transition of partial CoMoO 4 into Co(OH) 2 . CoO 6 octahedrons in both CoMoO 4 and Co(OH) 2 can transform pure CoOOH completely at lower potential, resulting in excess intrinsic activity whose summit is identified by overpotential at 10 mA cm −2 with 22.9% reduction and Tafel slope with 65.3% reduction. Well‐defined manipulation over the distorted polyhedrons offers one versatile knob to precisely modulate electronic structure of oxide catalysts with outstanding OER performance.