Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin University, Changchun, 130012, Jilin, PR China; School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, PR China.
Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin University, Changchun, 130012, Jilin, PR China.
Environ Pollut. 2021 Oct 1;286:117305. doi: 10.1016/j.envpol.2021.117305. Epub 2021 May 5.
In this study, heterojunction photocatalysts, XAg@C-TCZ, based on MOF-derived C-TiO and CdZnS decorated with Ag nanoparticles (Ag NPs) were successfully synthesized through hydrothermal and calcination methods. The catalytic effectiveness of XAg@C-TCZ was evaluated by simultaneous photocatalytic degradation of rhodamine B (RhB) and reduction of Cr(VI) under simulated sunlight irradiation. The presence of the Z-scheme heterojunction was demonstrated through trapping experiments, X-ray photoelectron spectroscopy (XPS), time-resolved photoluminescence (PL) investigations, and electron spin resonance (ESR) spectroscopy. With an initial RhB and Cr(VI) concentration of 7 mg L and 5 mg L, the catalyst 10Ag@C-TCZ achieved a simultaneous removal of 95.2% and 95.5% within 120 min, respectively. With the same catalyst, the degradation rate of RhB was 2.75 times higher and the reduction rate of Cr(VI) was 9.3 times higher compared to pure CdZnS. Total organic carbon (TOC) analysis confirmed the extent of mineralization of RhB, while the reduction of Cr(VI) was corroborated by XPS. Compared to pure RhB and Cr(VI) solutions, the reaction rates are smaller in the solution containing both contaminants, which is attributed to the competition for ·O. 10Ag@C-TCZ also exhibited a stable catalytic performance in tap water and lake water. This work provides a new perspective on the construction of heterojunctions with doped MOF derivatives for the purification of complex pollutant systems.
在这项研究中,通过水热和煅烧方法成功合成了基于 MOF 衍生的 C-TiO 和用 Ag 纳米粒子(Ag NPs)修饰的 CdZnS 的异质结光催化剂 XAg@C-TCZ。通过模拟阳光照射下罗丹明 B(RhB)的同时光催化降解和 Cr(VI)的还原来评估 XAg@C-TCZ 的催化效果。通过捕获实验、X 射线光电子能谱(XPS)、时间分辨光致发光(PL)研究和电子顺磁共振(ESR)光谱证明了 Z 型异质结的存在。在初始 RhB 和 Cr(VI)浓度分别为 7mg/L 和 5mg/L 的情况下,催化剂 10Ag@C-TCZ 在 120min 内分别实现了 95.2%和 95.5%的同时去除。在相同的催化剂下,与纯 CdZnS 相比,RhB 的降解速率提高了 2.75 倍,Cr(VI)的还原速率提高了 9.3 倍。总有机碳(TOC)分析证实了 RhB 的矿化程度,而 XPS 则证实了 Cr(VI)的还原。与纯 RhB 和 Cr(VI)溶液相比,在含有两种污染物的溶液中反应速率较小,这归因于·O 的竞争。10Ag@C-TCZ 在自来水和湖水 中也表现出稳定的催化性能。这项工作为用掺杂的 MOF 衍生物构建异质结以净化复杂的污染物系统提供了新的视角。