Lee Jin-Hyoek, Jeong Sang-Yun, Son Young-Don, Lee Sang-Wha
Chemical and Biological Engineering Department, Gachon University, Seongnam-si 13120, Republic of Korea.
Department of Biomedical Engineering, College of IT Convergence, Gachon University, Seongnam-si 13120, Republic of Korea.
Nanomaterials (Basel). 2023 May 6;13(9):1565. doi: 10.3390/nano13091565.
TiO₂ semiconductors exhibit a low catalytic activity level under visible light because of their large band gap and fast recombination of electron-hole pairs. This paper reports the simple fabrication of a 0D/2D heterojunction photocatalyst by anchoring TiO₂ quantum dots (QDs) on graphite-like C₃N₄ (g-C₃N₄) nanosheets (NSs); the photocatalyst is denoted as TiO₂ QDs@g-C₃N₄. The nanocomposite was characterized via analytical instruments, such as powder X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, t orange (MO) under solar light were compared. The TiO₂ QDs@g-C₃N₄ photocatalyst exhibited 95.57% MO degradation efficiency and ~3.3-fold and 5.7-fold higher activity level than those of TiO₂ QDs and g-C₃N₄ NSs, respectively. Zero-dimensional/two-dimensional heterojunction formation with a staggered electronic structure leads to the efficient separation of photogenerated charge carriers via a Z-scheme pathway, which significantly accelerates photocatalysis under solar light. This study provides a facile synthetic method for the rational design of 0D/2D heterojunction nanocomposites with enhanced solar-driven catalytic activity.
由于TiO₂半导体的带隙较大且电子-空穴对的复合速度较快,它们在可见光下表现出较低的催化活性水平。本文报道了一种通过将TiO₂量子点(QDs)锚定在类石墨C₃N₄(g-C₃N₄)纳米片(NSs)上简单制备0D/2D异质结光催化剂的方法;该光催化剂被标记为TiO₂ QDs@g-C₃N₄。通过粉末X射线衍射、X射线光电子能谱、扫描电子显微镜、透射电子显微镜等分析仪器对该纳米复合材料进行了表征。比较了其在太阳光下对甲基橙(MO)的光催化降解性能。TiO₂ QDs@g-C₃N₄光催化剂对MO的降解效率为95.57%,其活性水平分别比TiO₂ QDs和g-C₃N₄ NSs高约3.3倍和5.7倍。具有交错电子结构的零维/二维异质结的形成通过Z型途径导致光生电荷载流子的有效分离,这显著加速了太阳光下的光催化作用。本研究为合理设计具有增强的太阳能驱动催化活性的0D/2D异质结纳米复合材料提供了一种简便的合成方法。