Modulation of Photocatalytic CO2 Reduction by n–p Codoping Engineering of Single-Atom Catalysts

Abstract

Transition metal (TM) single-atom catalysts (SACs) have been widely applied in photocatalytic CO2 reduction. In this work, n–p codoping engineering is introduced to account for the modulation of photocatalytic CO2 reduction on a two-dimensional (2D) bismuth-oxyhalide-based cathode by using first-principles calculation. n–p codoping is established via the Coulomb interactions between the negatively charged TM SACs and the positively charged Cl vacancy (VCl) in the dopant–defect pairs. Based on the formation energy of charged defects, neutral dopant–defect pairs for the Fe, Co, and Ni SACs (PTM0) and the −1e charge state of the Cu SAC-based pair (PCu−1) are stable. The electrostatic attraction of the n–p codoping strengthens the stability and solubility of TM SACs by neutralizing the oppositely charged VCl defect and TM dopant. The n–p codoping stabilizes the electron accumulation around the TM SACs. Accumulated electrons modify the d-orbital alignment and shift the d-band center toward the Fermi level, enhancing the reducing capacity of TM SACs based on the d-band theory. Besides the electrostatic attraction of the n–p codoping, the PCu−1 also accumulates additional electrons surrounding Cu SACs and forms a half-occupied dx2−y2 state, which further upshifts the d-band center and improves photocatalytic CO2 reduction. The metastability of Cl multivacancies limits the concentration of the n–p pairs with Cl multivacancies (PTM@nCl (n > 1)). Positively charged centers around the PTM@nCl (n > 1) hinders the CO2 reduction by shielding the charge transfer to the CO2 molecule.