Search

Constructing nitrogen (N2) adsorption and activation sites on semiconductors is the key to achieving efficient N2 photofixation. Herein, Mn–W dual‐metal sites on WO3 are designed toward efficient N2 photoreduction via controlled Mn doping. Impressively, the optimal 2.3% Mn‐doped WO3 (Mn‐WO3) exhibits a remarkable ammonia (NH3) production rate of 425 µmol gcat.−1 h−1, representing the best catalytic performance among the ever‐reported tungsten oxide‐based photocatalysts for N2 fixation. Quasi in situ synchrotron radiation X‐ray spectroscopy directly identifies that the Mn–W dual‐metal sites can enhance the polarization of the adsorbed N2, which is beneficial to the N2 activation. Further theoretical calculations reveal that the increased polarization is originated from the electron back‐donation into the antibonding orbitals of the adsorbed N2, hence lowering the reaction energy barrier toward the N2 photofixation. The concept of dual sites construction for inert molecule activation offers a powerful platform toward rational design of highly efficient catalysts for nitrogen fixation and beyond. [ABSTRACT FROM AUTHOR]

Keywords: grain boundary; N2 fixation; operando oxygen vacancies; photocatalysis; WO3 In article number 1902319, Xusheng Zheng, Shuquan Liang, Liangbing Wang, and co-workers report that grain boundaries (GBs) in nanoporous WO SB 3 sb induce many operando oxygen vacancies under light irradiation. Grain boundary, N2 fixation, operando oxygen vacancies, photocatalysis, WO3. [Extracted from the article]