Abstract

Here, we demonstrate that structural defects can induce catalytic reactivity in simple metal oxides to deliver cost-effective alternatives to noble metal group catalysts. We detail a strategy for introducing multiple defect sites in a binary TiO2–SiO2 composite to invoke synergism for oxygen activation. Hydrogenation and UV light pretreatment were applied to generate two distinct and adjacent defect sites, Ti3+ and silica-based nonbridging oxygen hole centers (NBOHC)—which work in unison to activate oxygen and oxidize formic acid under ambient conditions without light. The hydrogenation step was found to be crucial for rupturing Ti–O–Si bonds while first-principles calculations indicated that Si-doped TiO2 lowered the energy barrier for oxygen activation and formic acid dehydrogenation on the defect sites. Activity lost during the reaction was recoverable by catalyst reillumination. Defective metal oxides represent an appealing prospect in the pursuit of simple and readily accessible catalyst materials.

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