Liu Linlin, Song Xingyue, Kong Xiangxin, Duan Qian, Zhu Enwei
School of Materials Science and Engineering, Changchun University of Science and Technology Changchun 130022 P. R. China
Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University Changchun 130103 P. R. China.
RSC Adv. 2020 Mar 3;10(15):9116-9125. doi: 10.1039/d0ra00960a. eCollection 2020 Feb 27.
In this research work, we successfully fabricated a range of PTET-T-COOH/g-CN heterostructures a simple method. The as-prepared PTET-T-COOH/g-CN heterostructures show enhanced photocatalytic degradation activity as compared to pure g-CN. For the photocatalytic degradation of RhB, the optimal PTET-T-COOH/g-CN-1% heterostructure is nearly 3.83 times that of the pure g-CN. The enhancement of photocatalytic performance is ascribed to three aspects: one is the strong interaction between PTET-T-COOH and g-CN; the second is the larger surface area of the PTET-T-COOH/g-CN heterostructure compared to that of pure g-CN; the third is the effectively improved transferability of photogenerated carriers. In addition, the whole photocatalytic reaction mechanism over the PTET-T-COOH/g-CN heterostructure is provided. This work may offer a hopeful method to synthesize any other heterostructure with high stability and superior photocatalytic activity.
在这项研究工作中,我们通过一种简单的方法成功制备了一系列PTET-T-COOH/g-CN异质结构。与纯g-CN相比,所制备的PTET-T-COOH/g-CN异质结构表现出增强的光催化降解活性。对于RhB的光催化降解,最佳的PTET-T-COOH/g-CN-1%异质结构的活性几乎是纯g-CN的3.83倍。光催化性能的增强归因于三个方面:一是PTET-T-COOH与g-CN之间的强相互作用;二是PTET-T-COOH/g-CN异质结构比纯g-CN具有更大的表面积;三是光生载流子的转移能力得到有效提高。此外,还给出了PTET-T-COOH/g-CN异质结构上的整个光催化反应机理。这项工作可能为合成任何其他具有高稳定性和优异光催化活性的异质结构提供一种有前景的方法。