Activating Inert Alkali-Metal Ions by Electron Transfer from Manganese Oxide for Formaldehyde Abatement.

Abstract

Alkali-metal ions often act as promoters rather than active components due to their stable outermost electronic configurations and their inert properties in heterogeneous catalysis. Herein, inert alkali-metal ions, such as K+ and Rb+ , are activated by electron transfer from a Hollandite-type manganese oxide (HMO) support for HCHO oxidation. Results from synchrotron X-ray diffraction, absorption, and photoelectron spectroscopies demonstrate that the electronic density of states of single alkali-metal adatoms is much higher than that of K+ or Rb+ , because electrons transfer from manganese to the alkali-metal adatoms through bridging lattice oxygen atoms. Electron transfer originates from the interactions of alkali metal d-sp frontier orbitals with lattice oxygen sp3 orbitals occupied by lone-pair electrons. Reaction kinetics data of HCHO oxidation reveal that the high electronic density of states of single alkali-metal adatoms is favorable for the activation of molecular oxygen. Mn L3 -edge and O K-edge soft-X-ray absorption spectra demonstrate that lattice oxygen partially gains electrons from the Mn eg orbitals, which leads to the upshift in energy of lattice oxygen orbitals. Therefore, the facile activation of molecular oxygen by the electron-abundant alkali-metal adatoms and active lattice oxygen are responsible for the high catalytic activity in complete oxidation of HCHO. This work could assist the design of efficient and cheap catalysts by tuning the electronic states of active components.