Tailoring Oxygen Vacancies and Active Surface Oxygen Species in Copper-Doped MnO<sub>2</sub> Catalysts for Total Catalytic Oxidation of VOCs
Minh Tuan Nguyen Dinh, Chinh Chien Nguyen, Nga Phan Thị Hằng, Hoang Duy Nguyen Phuc, Quyet Van Le, Soo Young Kim, Lam Nguyen‐Dinh
Abstract
Catalytic oxidation has been considered an essential route to tackle volatile organic compounds (VOCs)-driven pollution. To this point, surface engineering has emerged as a robust pathway to promote the efficiency of MnO 2 -based materials toward VOC oxidation. However, regulating such surface properties has been a critical challenge. This investigation attempts to tailor surface oxygen vacancies and active surface oxygen for the total catalytic oxidation of various VOCs (e.g., formaldehyde, isopropanol, and toluene) via doping copper into cryptomelane and birnessite-type MnO 2 catalysts. The catalysts are synthesized by a novel facile successive redox precipitation method between KMnO 4 and an ethanol solution containing copper nitrate precursors, followed by annealing. It turns out that the low amount of Cu dopants, corresponding to the copper-to-manganese ratio of 0.17 ( R Cu/Mn = 0.17), generates a tunnel-structured cryptomelane-type MnO 2 with strong bulk oxygen mobility. Such a crystalline structure exhibits the best catalytic performance for the total catalytic oxidation of toluene. The higher copper loading ( R Cu/Mn = 0.27–0.34) drives the formation of Cu-doped layered birnessite-type MnO 2 materials containing rich oxygen vacancies and high active surface oxygen species. Those catalysts promote the oxidation of isopropanol and formaldehyde, respectively. To this end, oxygen vacancies and surface oxygen species crucially steer the molecular oxygen activation and interactions toward adsorbed oxygen species, significantly promoting the total oxidation of isopropanol and formaldehyde, respectively. The explored finding could disclose an outstanding platform toward highly selective and efficient oxidation of VOCs.