In-situ growth of TiO2@B-doped g-C3N4 core-shell nanospheres for boosts the photocatalytic detoxification of emerging pollutants with mechanistic insight

光催化 材料科学 罗丹明B 光致发光 光电流 化学工程 X射线光电子能谱 氧化物 纳米技术 兴奋剂 石墨氮化碳 化学 有机化学 催化作用 光电子学 工程类 冶金
作者
Vellaichamy Balakumar,S. Selvarajan,Baishnisha Amanulla,Sellamuthu Kathiresan
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:577: 151924-151924 被引量:25
标识
DOI:10.1016/j.apsusc.2021.151924
摘要

This study demonstrated an in-situ hydrothermal synthesis method to develop unique core-shell nanospheres, TiO 2 @B-doped g-C 3 N 4 Z-scheme photocatalyst for efficient detoxification of emerging organic and pharmaceutical hazards. • TiO 2 @B-doped g-C 3 N 4 (TOBCN) were synthesized via an in-situ hydrothermal method. • The TOBCN (2) photocatalyst exhibits good photocatalytic performance and stability. • More reaction sites and high surface area were attained on TOBCN (2) • The photocatalyst possess excellent photocatalytic reusability and stability. The photocatalysts charge transportation and separation abilities are two critical factors for the efficient detoxification of organic and pharmaceutical hazards. This study demonstrated an in-situ hydrothermal synthesis method to develop unique core-shell nanospheres, TiO 2 @B-doped g-C 3 N 4 (TOBCN (1-3)) Z-scheme photocatalyst. The TOBCN were characterized by using X-ray powder diffraction, FT-IR, SEM, TEM, EDX with mapping analysis, XPS and UV-DRS. In particular, under optimized ratio, synthesized TOBCN (2) photocatalyst showed an excellent detoxification ability of both toxic organic (rhodamine-B (Rh-B)) and pharmaceutical levofloxacin (LF) via synergistic interfacial effects of TiO 2 core with BCN shell. At the same time, lower detoxification results were also observed when compared with TOBCN (1), TOBCN (3), pure TiO 2 and BCN in terms of the efficiency and kinetic rate constant. The BET, photoluminescence, photocurrent and impedance analysis also revealed an improved surface area of active sites, efficient charge separation and subsequent charge transfer of photocatalyst, respectively. Further, the photo detoxification mechanisms, generated reactive species and stability of the photocatalyst were also elucidated and discussed in detail. This work emphasized that the prepared core (metal oxide)-shell (carbon) material has great potential as an efficient photocatalysts for detoxification of hazards and beyond.
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