Oxygen Vacancy Generation and Stabilization in CeO2–x by Cu Introduction with Improved CO2 Photocatalytic Reduction Activity
Introducing O vacancies into the lattice of a semiconductor photocatalyst can alter its intrinsic electronic properties and band gap, thus enhancing the visible light absorption, promoting the separation/transfer of photogenerated charge carriers, and resultantly elevating the photocatalytic activit...
Gespeichert in:
Veröffentlicht in: | ACS catalysis 2019-05, Vol.9 (5), p.4573-4581 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Introducing O vacancies into the lattice of a semiconductor photocatalyst can alter its intrinsic electronic properties and band gap, thus enhancing the visible light absorption, promoting the separation/transfer of photogenerated charge carriers, and resultantly elevating the photocatalytic activity of oxide semiconductors. Moreover, O vacancies can help adsorb and activate CO2 on photocatalyst surfaces, which, however, are prone to being filled by O atoms during the photoreduction reaction. In this work, Cu was introduced to increase the O vacancy concentration in CeO2–x and promote the photocatalytic activity of CeO2–x . The sample Cu/CeO2–x -0.1 showed the highest photocatalytic activity with a CO yield of 8.25 μmol g–1 under 5 h irradiation, which is ∼26 times that on CeO2–x . According to the analysis of Raman and X-ray photoelectron spectroscopy (XPS) spectra, it has been evidenced that Cu introduction benefits the chemical stabilization of O vacancies in CeO2–x during photocatalytic CO2 reduction, which is responsible for the improved and sustained photocatalytic activity. |
---|---|
ISSN: | 2155-5435 2155-5435 |
DOI: | 10.1021/acscatal.8b03975 |