石墨氮化碳
光催化
纳米颗粒
材料科学
傅里叶变换红外光谱
异质结
催化作用
化学工程
二氧化锡
氮化物
化学
X射线光电子能谱
罗丹明B
纳米技术
光电子学
冶金
工程类
生物化学
图层(电子)
作者
Dai‐Phat Bui,Thanh-Dat Nguyen,Thi Thuy Le Vo,Cao Minh Thi,Sheng‐Jie You,Viet Van Pham
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2021-08-30
卷期号:4 (9): 9333-9343
被引量:30
标识
DOI:10.1021/acsanm.1c01801
摘要
Designing a heterojunction that can effectively degrade pollutants under different reaction conditions remains a challenge and question. Herein, an S-scheme model of oxygen-vacancies-defected tin dioxide nanoparticles and graphitic carbon nitride (SnO2–x/g-C3N4) is fabricated. This is also the first study activating photocatalysts by potassium peroxymonosulfate (PMS) for degrading rhodamine B (RhB) dye. Empirical evidence, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared spectroscopy (FTIR), show the presence and a combination of SnO2–x nanoparticles and g-C3N4 nanosheets. Optical, electrochemical analysis, and trapping experiments reveal the contribution of different charge states of oxygen vacancies, a visible light responsibility of 3.2 eV, and an S-scheme charge transfer to the strengthened photocatalytic performance of SnO2–x/g-C3N4. Besides, an S-scheme is accelerated to higher performance from 20% to 99.8% RhB 20 mg L–1 degradation via activating PMS in solution. This design and activation may promise applications in efficient water treatment.
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