Pedrosa Marta, Da Silva Eliana S, Pastrana-Martínez Luisa M, Drazic Goran, Falaras Polycarpos, Faria Joaquim L, Figueiredo José L, Silva Adrián M T
Laboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials (LSRE-LCM), Faculdade de Engenharia, Universidade do Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal.
Carbon Materials Research Group, Department of Inorganic Chemistry, Faculty of Sciences, University of Granada, Campus Fuentenueva s/n, 18071 Granada, Spain.
J Colloid Interface Sci. 2020 May 1;567:243-255. doi: 10.1016/j.jcis.2020.01.093. Epub 2020 Jan 27.
Undoped metal-free graphene oxide (GO) materials prepared by either a modified Hummers' (GO-H) or a Brodie's (GO-B) method were tested as photocatalysts in aqueous solution for the oxidative conversion of phenol. In the dark, the adsorptive capacity of GO-B towards phenol (35%) was higher than that of GO-H (15%). Upon near-UV/Vis irradiation, GO-H was able to remove 21% of phenol after 180 min, mostly through adsorption. On the other hand, by using less energetic visible irradiation, GO-B removed as much as 95% in just 90 min. By thorough characterization of the prepared materials (SEM, HRTEM, TGA, TPD, Raman, XRD, XPS and photoluminescence) the observed performances could be explained in terms of their different surface chemistries. The GO-B presents the lower concentration of oxygen functional groups (in particular carbonyl groups as revealed by XPS) and it has a considerably higher photocatalytic activity compared to GO-H. Photoluminescence (PL) of liquid dispersions and XRD analysis of powders showed lower PL intensity and smaller interlayer distance for GO-B relative to GO-H, respectively: this suggests lower electron-hole recombination and enhanced electron transfer in GO-B, in support of its boosted photocatalytic activity. Reusability tests showed no efficiency loss after a second usage cycle and over three runs under visible irradiation, which was in line with the similarity of the XPS spectra of the fresh and used GO-B materials. Moreover, scavenging studies revealed that holes and hydroxyl radicals were the main reactive species in play during the photocatalytic process. The obtained results, establish for the first time, that GO prepared by Brodie's method is an active and stable undoped metal-free photocatalyst for phenol degradation in aqueous solutions, opening new paths for the application of more sustainable and metal-free materials for water treatment solutions.
通过改进的Hummers法(GO-H)或Brodie法(GO-B)制备的未掺杂无金属氧化石墨烯(GO)材料,在水溶液中作为光催化剂用于苯酚的氧化转化测试。在黑暗中,GO-B对苯酚的吸附容量(约35%)高于GO-H(约15%)。在近紫外/可见光照射下,GO-H在180分钟后能够去除21%的苯酚,主要是通过吸附。另一方面,使用能量较低的可见光照射时,GO-B在仅90分钟内就能去除高达95%的苯酚。通过对制备材料进行全面表征(扫描电子显微镜、高分辨率透射电子显微镜、热重分析、程序升温脱附、拉曼光谱、X射线衍射、X射线光电子能谱和光致发光),观察到的性能差异可以根据它们不同的表面化学性质来解释。GO-B的氧官能团浓度较低(特别是X射线光电子能谱显示的羰基),与GO-H相比,它具有相当高的光催化活性。液体分散体的光致发光(PL)和粉末的X射线衍射分析表明,相对于GO-H,GO-B的PL强度较低,层间距较小:这表明GO-B中电子-空穴复合较少,电子转移增强,支持了其增强的光催化活性。可重复使用性测试表明,在第二次使用循环后以及在可见光照射下进行三次运行后,效率没有损失,这与新鲜和使用过的GO-B材料的X射线光电子能谱相似性一致。此外,清除研究表明,空穴和羟基自由基是光催化过程中的主要活性物种。所获得的结果首次证实,通过Brodie法制备的GO是一种用于水溶液中苯酚降解的活性且稳定的未掺杂无金属光催化剂,为应用更具可持续性的无金属材料处理水处理解决方案开辟了新途径。