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凝胶状碳点:一种高性能的未来光催化剂。

Gel-like carbon dots: A high-performance future photocatalyst.

作者信息

Zhou Yiqun, ElMetwally Ahmed E, Chen Jiuyan, Shi Wenquan, Cilingir Emel K, Walters Brian, Mintz Keenan J, Martin Christian, Ferreira Braulio C L B, Zhang Wei, Hettiarachchi Sajini D, Serafim Leonardo F, Blackwelder Patricia L, Wikramanayake Athula H, Peng Zhili, Leblanc Roger M

机构信息

Department of Chemistry, University of Miami, Coral Gables, FL 33146, USA.

Department of Chemistry, University of Miami, Coral Gables, FL 33146, USA; Petrochemicals Department, Egyptian Petroleum Research Institute, Nasr City, Cairo 11727, Egypt.

出版信息

J Colloid Interface Sci. 2021 Oct;599:519-532. doi: 10.1016/j.jcis.2021.04.121. Epub 2021 Apr 28.

DOI:10.1016/j.jcis.2021.04.121
PMID:33964697
Abstract

To protect water resources, halt waterborne diseases, and prevent future water crises, photocatalytic degradation of water pollutants arouse worldwide interest. However, considering the low degradation efficiency and risk of secondary pollution displayed by most metal-based photocatalysts, highly efficient and environmentally friendly photocatalysts with appropriate band gap, such as carbon dots (CDs), are in urgent demand. In this study, the photocatalytic activity of gel-like CDs (G-CDs) was studied using diverse water pollution models for photocatalytic degradation. The degradation rate constants demonstrated a remarkably enhanced photocatalytic activity of G-CDs compared with most known CD species and comparability to graphitic carbon nitride (g-CN). In addition, the rate constant was further improved by 1.4 times through the embedment of g-CN in G-CDs to obtain CD-CN. Significantly, the rate constant was also higher than that of g-CN alone, revealing a synergistic effect. Moreover, the use of diverse radical scavengers suggested that the main contributors to the photocatalytic degradation with G-CDs alone were superoxide radicals (O) and holes that were, however, substituted by O and hydroxyl radicals (OH) due to the addition of g-CN. Furthermore, the photocatalytic stabilities of G-CDs and CD-CN turned out to be excellent after four cycles of dye degradation were performed continuously. Eventually, the nontoxicity and environmental friendliness of G-CDs and CD-CN were displayed with sea urchin cytotoxicity tests. Hence, through various characterizations, photocatalytic degradation and cytotoxicity tests, G-CDs proved to be an environmentally friendly and highly efficient future photocatalyst.

摘要

为了保护水资源、遏制水传播疾病并防止未来的水危机,水污染物的光催化降解引起了全球关注。然而,考虑到大多数金属基光催化剂表现出的低降解效率和二次污染风险,迫切需要具有合适带隙的高效且环境友好的光催化剂,如碳点(CDs)。在本研究中,使用多种水污染模型对凝胶状碳点(G-CDs)的光催化活性进行了光催化降解研究。降解速率常数表明,与大多数已知的碳点种类相比,G-CDs的光催化活性显著增强,且与石墨相氮化碳(g-CN)相当。此外,通过将g-CN嵌入G-CDs中得到CD-CN,速率常数进一步提高了1.4倍。值得注意的是,该速率常数也高于单独的g-CN,显示出协同效应。此外,使用多种自由基清除剂表明,单独使用G-CDs进行光催化降解的主要贡献者是超氧自由基(O)和空穴,然而,由于添加了g-CN,它们被O和羟基自由基(OH)所取代。此外,在连续进行四个染料降解循环后,G-CDs和CD-CN的光催化稳定性表现出色。最终,通过海胆细胞毒性试验显示了G-CDs和CD-CN的无毒和环境友好性。因此,通过各种表征、光催化降解和细胞毒性试验,G-CDs被证明是一种环境友好且高效的未来光催化剂。

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