Synergistic introduction of oxygen vacancy and silver/silver iodide: Realizing deep structure regulation on bismuth oxybromide for robust carbon dioxide reduction and pollutant oxidation.

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Title: Synergistic introduction of oxygen vacancy and silver/silver iodide: Realizing deep structure regulation on bismuth oxybromide for robust carbon dioxide reduction and pollutant oxidation.
Authors: Jia, Xuemei1 (AUTHOR) xuemeijia@njust.edu.cn, Lin, Haili1 (AUTHOR), Cao, Jing1 (AUTHOR) caojing@chnu.edu.cn, Hu, Cheng1 (AUTHOR), Sun, Haoyu1 (AUTHOR), Chen, Shifu1 (AUTHOR)
Source: Journal of Colloid & Interface Science. Oct2022, Vol. 624, p181-195. 15p.
Subjects: Carbon dioxide reduction, Pollutants, Silver iodide, Bismuth, X-ray photoelectron spectroscopy, Silver, Carbon monoxide, Density functional theory
Abstract: A bifunctional S-scheme BiOBr-based heterojunction with high effective CO 2 reduction and antibiotic TC removal under visible light was designed by the cooperative introduction of oxygen vacancies (OVs) and Ag/AgI, in which OVs acted as the charge transmission bridge to reduce the interface migration resistance of the charge meanwhile Ag/AgI served as cocatalyst to enhance the separation efficiency of carriers. [Display omitted] • Synergistic introduction of surface OVs and Ag/AgI realized deep structure regulation on BiOBr. • S-scheme Ag/AgI/BiO 1− x Br could preserve strong redox capacity of holes and electrons. • OVs as the charge transmission bridge reduced the interface migration resistance of the charge. • Ag/AgI as a cocatalyst enhanced the separation efficiency of carriers. • Ag/AgI/BiO 1− x Br displayed outstanding photoreactivity for CO 2 reduction and TC removal. To efficiently solve severe energy shortage and environmental pollution issues, step-scheme (S-scheme) photocatalytic system, as perfect photocatalyst with strong redox ability and swift separation efficiency of carriers, has been considered a feasible tactic. Herein, a novel S-scheme silver/silver iodide/bismuth oxybromide heterojunction with rich oxygen vacancies (OVs) (labeled as Ag/AgI/BiO 1− x Br) was in situ fabricated via a simple photodeposition-precipitation method. It was discovered that the obtained Ag/AgI/BiO 1− x Br heterojunction with the optimized molar ratio of silver/bismuth (Ag/Bi) at 0.4 presented excellent photocatalytic properties for carbon dioxide (CO 2) reduction (2.46 μmol g−1h−1 carbon monoxide (CO) and 1.25 μmol g−1h−1 methane (CH 4) generation) and antibiotic tetracycline (TC) removal (96.7%) even in actual waste water or in the presence of electrolytes. The enhanced performance of S-scheme Ag/AgI/BiO 1− x Br composite may be ascribed to the collaborative effect of OVs and silver/silver iodide (Ag/AgI), in which OVs acted as the charge transmission bridge for reducing the interface migration resistance of the charge and Ag/AgI served as a cocatalyst for enhancing the separation efficiency of carriers. Furthermore, a feasible photocatalytic mechanism was discussed via density functional theory calculation and in-situ X-ray photoelectron spectroscopy. This work not only demonstrated the synergistic application of OVs transmission bridge and Ag/AgI cocatalyst, but also provided a facile way to design high-efficiency and stable photocatalysts for energy production and environmental remediation. [ABSTRACT FROM AUTHOR]
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Database: Engineering Source
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