A comprehensive review on the boosted effects of anion vacancy in the heterogeneous photocatalytic degradation, part I: Focus on sulfur, nitrogen, carbon, and halogen vacancies.

Ecotoxicol Environ Saf

Department of Chemistry, Shahreza Branch, Islamic Azad University, P.O. Box 311-86145, Shahreza, Isfahan, Iran; Department of Chemistry, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan, Iran.

Published: January 2024

The greenest environmental remediation way is the photocatalytic degradation of organic pollutants. However, limited photocatalytic applications are due to poor sunlight absorption and photogenerated charge carriers' recombination. These limitations can be overcome by introducing anion vacancy (AV) (O, S, N, C, and Halogen) defects in semiconductors that enhance light harvesting, facilitate charge separation, modulate electronic structure, and produce reactive radicals. In continuing part A of this review, in this part, we summarized the recent AVs' research, including S, N, C, and halogen vacancies on the boosted photocatalytic features of semiconductor materials, like metal oxides/sulfides, oxyhalides, and nitrides in detail. Also, we outline the recently developed AV designs for the photocatalytic degradation of organic pollutants. The AV creating and analysis methods and the recent photocatalytic applications and mechanisms of AV-mediated photocatalysts are reviewed. AV engineering photocatalysts' challenges and development prospects are illustrated to get a promising research direction.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ecoenv.2024.115927DOI Listing

Publication Analysis

Top Keywords

photocatalytic degradation
12
anion vacancy
8
halogen vacancies
8
degradation organic
8
organic pollutants
8
photocatalytic applications
8
photocatalytic
6
comprehensive review
4
review boosted
4
boosted effects
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!