Bare undoped nontoxic carbon dots as a visible light photocatalyst for the degradation of methylene blue and congo red

光催化 刚果红 亚甲蓝 光化学 核化学 可见光谱 反应速率常数 化学 碳纤维 X射线光电子能谱 材料科学 催化作用 有机化学 化学工程 动力学 吸附 物理 光电子学 量子力学 复合数 工程类 复合材料
作者
Ambreen Abbasi,M. Abushad,Arisha Khan,Zia Ul Haq Bhat,Summaiya Hanif,Mohammad Shakir
出处
期刊:Carbon trends [Elsevier]
卷期号:10: 100238-100238 被引量:14
标识
DOI:10.1016/j.cartre.2022.100238
摘要

Rampant discharge of industrial wastes containing non-biodegradable colored dyes to water bodies has prompted the development of an environment-friendly photocatalytic process using nontoxic, photostable water soluble photocatalyst. In this work, bare undoped carbon dots (CDots) based photocatalyst has been reported. The carbon dots were synthesized via the pyrolysis method using a single source, ammonium citrate; the reported carbon dots were characterized using HR-TEM, XRD, FTIR, XPS, Photoluminescence (P.L.), TGA, and UV–Vis spectroscopy. The catalytic behavior of the synthesized carbon dots was tested against two water-soluble industrial dyes (Methylene Blue (M.B.) and Congo Red (C.R.)). The synthesized carbon dots exhibited excellent photocatalytic activity under visible light irradiation facilitating 96% degradation of MB within 55 min and 98% degradation of C.R. within 60 min. A plausible mechanism for the photocatalytic degradation of studied dyes was proposed based on comprehensive active species trapping experiments. The photogenerated holes (h+) and superoxide radicals (O2 .−) were the main active species responsible for the degradation of studied dyes. The kinetic studies revealed that the cationic methylene blue dye degradation by BUCDs followed the modified Freundlich kinetic model with rate constant 0.063 and anionic congo red dye depicted closed correlation with both parabolic diffusion model and modified Freundlich kinetic model with rate constants 0.256 and 0.196. The synthesized BUCDs showed no cytotoxicity in HCT human colon cancer cell lines, thus establishing their nontoxic nature.
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