氧化还原
罗丹明B
降级(电信)
光催化
异质结
盐酸四环素
材料科学
化学工程
催化作用
石墨氮化碳
光化学
可见光谱
吸收(声学)
激进的
聚合
热氧化
氮化碳
热稳定性
核化学
碳纤维
化学气相沉积
化学
无机化学
热处理
比表面积
盐酸盐
作者
Shuangyu Wang,Jianqiang Wang,Ping Yang,Xiao Zhang
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-06-24
卷期号:42 (26): 18991-19003
被引量:5
标识
DOI:10.1021/acs.langmuir.6c01711
摘要
The redox ability of photocatalysts is a key to the degradation of tetracycline hydrochloride (TCH) which resulted in serious environmental problems. In this paper, narrow band gap BiOBr nanoplates were grown on superior thin graphitic carbon nitride (g-C 3 N 4 ) nanosheets to increase light absorption and enhance redox ability for TCH removal. Meanwhile, g-C 3 N 4 nanosheets were created by a two-step thermal polymerization at 600 and 700 °C, respectively. The deposition of layered BiOBr was finished along the surface of g-C 3 N 4 nanosheets by a direct wet-chemical precipitation. BiOBr nanoplates were in situ grown on g-C 3 N 4 nanosheets to create a well-developed interface and form S-scheme BiOBr/g-C 3 N 4 heterostructures with enhanced photocatalytic performance. Visible light-derived photocatalytic tests indicated that the heterostructure sample created using optimized conditions revealed excellent performance, in which Rhodamine B of 10 mg/L was completely degraded within 9 min (10 mg catalyst added). TCH (50 mg/L) of 80% was degraded within 60 min with a degradation rate of 2.4 × 10 –2 min –1, which was 6 and 3.4 times of those of pristine g-C 3 N 4 nanosheets and BiOBr, respectively. The free radical capture test suggested that superoxide radicals dominated TCH degradation, and cyclic stability test indicated the degradation rate was kept 72% after 6 cycles. The S-scheme pathway in the heterostructure-enhanced charge separation and retained high redox ability for photocatalytic degradation of pollutants. These results supplied useful approaches for the photocatalysts with a high redox ability.
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