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具有改善的可见光光催化降解亚甲基蓝性能的S型硫化镉/石墨相氮化碳纳米复合材料的构建

Construction of S-scheme CdS/g-CN nanocomposite with improved visible-light photocatalytic degradation of methylene blue.

作者信息

Van Kim Nguyen, Huu Ha Tran, Nguyen Thi Viet Nga, Thi Le Thanh-Lieu, Hoang Quoc Dat, Dinh Quoc Viet, Vo Vien, Tran Dai Lam, Vasseghian Yasser

机构信息

Faculty of Natural Sciences, Quy Nhon University, Quy Nhon, 55000, Binh Dinh, Viet Nam.

Faculty of Natural Sciences, Quy Nhon University, Quy Nhon, 55000, Binh Dinh, Viet Nam.

出版信息

Environ Res. 2022 Apr 15;206:112556. doi: 10.1016/j.envres.2021.112556. Epub 2021 Dec 22.

Abstract

Within moderate band gap, g-CN and CdS are both promising visible light driven photocatalysts. However, their intrinsic high recombination rate of photo-induced electron-hole pairs along with the poor susceptibility in photocorrosion of CdS is main limitations hindering their practical application. In this study, the CdS/g-CN composites with various weight ratios of CdS to g-CN were solvothermal prepared from the dispersion of components, g-CN and CdS, in ethanol. The physicochemical characterizations demonstrate the success in the fabrication of well-dispersed CdS nanoparticles in the g-CN matrix. The enhanced photocatalytic activity of the g-CN/CdS composite over the degradation of methylene blue under visible light was ascribed to the effective photo-induced electron-hole separation via the step scheme (S-scheme) pathway in which the main contribution of high oxidative hydroxyl radicals (OH) was demonstrated. Furthermore, via S-scheme model, we also clarify the depletion of photo-induced holes on CdS which is ascribed as the reason for improvement in resistance to photocorrosion of composites.

摘要

在中等带隙范围内,g-CN和CdS都是很有前景的可见光驱动光催化剂。然而,它们固有的光生电子-空穴对复合率高,以及CdS光腐蚀敏感性差,是阻碍它们实际应用的主要限制因素。在本研究中,通过将g-CN和CdS组分分散在乙醇中,采用溶剂热法制备了具有不同CdS与g-CN重量比的CdS/g-CN复合材料。物理化学表征表明,成功地在g-CN基体中制备了分散良好的CdS纳米颗粒。g-CN/CdS复合材料在可见光下对亚甲基蓝降解的光催化活性增强,归因于通过阶梯式(S-型)途径实现的有效光生电子-空穴分离,其中高氧化性羟基自由基(OH)起主要作用。此外,通过S-型模型,我们还阐明了CdS上光生空穴的消耗,这被认为是复合材料抗光腐蚀性能提高的原因。

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