Please use this identifier to cite or link to this item:
Title: Oxygen vacancy engineering of Bi2O3/Bi2O2CO3 heterojunctions : implications of the interfacial charge transfer, NO adsorption and removal
Authors: Lu, YF
Huang, Y
Zhang, YF
Cao, JJ
Li, HW 
Bian, C
Lee, SC 
Keywords: Oxygen vacancy
Bi2O3/Bi2O2CO3 heterojunction
Charge separation
NO enrichment and removal
Issue Date: 2018
Publisher: Elsevier
Source: Applied catalysis B : environmental, 5 Sept. 2018, v. 231, p. 357-367 How to cite?
Journal: Applied catalysis B : environmental 
Abstract: Efficient enrichment of targeted gaseous pollutants and fast diffusion rates of charge carriers are essential for the photocatalytic removal of nitric oxides at ambient concentration levels. Here we demonstrate that the construction of nano-structured Bi2O3/Bi2O2CO3 heterojunctions with oxygen vacancies, increasing the photocatalytic NO removal activity, durability and selectivity for final products nitrate formation. Combining the experimental and density-functional theory calculations, it was elucidated that the presence of surface oxygen vacancies not only work as adsorption sites of low concentration NO, but also offer an intimate and integrated structure between surface defects and the light-harvesting heterojunctions, which can facilitate solar energy conversion and charge carrier transfer (more than 2 times). Control experiments with pristine Bi2O3/Bi2O2CO3 also confirmed the crucial role of surface oxygen vacancies on the improvement of NO adsorption and removal ability during the photocatalytic degradation process. We explain the enhanced removal of NO through the synergistic effect of oxygen vacancy and heterojunction, which not only guaranteed the generation of more center dot OH radicals, but also provided another route to produce hydrogen peroxide. Our findings may provide an opportunity to develop a promising catalyst for air pollution control.
ISSN: 0926-3373
EISSN: 1873-3883
DOI: 10.1016/j.apcatb.2018.01.008
Appears in Collections:Journal/Magazine Article

View full-text via PolyU eLinks SFX Query
Show full item record


Citations as of Jan 11, 2019


Citations as of Jan 14, 2019

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.