Liu Shuanghong, Huang Guan, Wang Jiefei, Bao Jianshuai, Wang Mengyue, Wei Yaqun, Zhong Yong, Bai Feng
Key Laboratory for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-Efficiency Display and Lighting Technology, School of Materials Science and Engineering, Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng 475004, China.
International Joint Centre for Biomedical Innovation, School of Life Sciences, Henan University, Kaifeng 475004, China.
Nanomaterials (Basel). 2023 Feb 8;13(4):660. doi: 10.3390/nano13040660.
Surface plasmon resonance (SPR) photocatalysts have attracted considerable attention because of their strong absorption capacity of visible light and enhanced photogenic carrier separation efficiency. However, the separate production of metal nanoparticles (NPs) and semiconductors limits the photogenic charge transfer. As one of the most promising organic photocatalysts, porphyrin self-assemblies with a long-range ordered structure-enhance electron transfer. In this study, plasmonic noble metal-based porphyrin hexagonal submicrowires composites (M-HW) loaded with platinum (Pt), silver (Ag), gold (Au), and palladium (Pd) NPs were synthesized through a simple in situ photocatalytic method. Homogeneous and uniformly distributed metal particles on the M-HW composites enhanced the catalytic or chemical properties of the organic functional nanostructures. Under the same loading of metal NPs, the methyl orange photocatalytic degradation efficiency of Ag-HW [k (0.043 min)] composite was three times higher than that of HW, followed by Pt-HW [k (0.0417 min)], Au-HW [k (0.0312 min)], and Pd-HW [k (0.0198 min)]. However, the rhodamine B (RhB) and eosin B photocatalytic degradations of Pt-HW were 4 times and 2.6 times those of HW, respectively. Finally, the SPR-induced electron injection, trapping, and recombination processes of the M-HW system were investigated. These results showed that M-HW plasmonic photocatalysts exhibited excellent photocatalytic performances, making them promising materials for photodegrading organic pollutants.
表面等离子体共振(SPR)光催化剂因其对可见光的强吸收能力和增强的光生载流子分离效率而备受关注。然而,金属纳米颗粒(NPs)和半导体的单独生产限制了光生电荷转移。作为最有前途的有机光催化剂之一,具有长程有序结构的卟啉自组装体增强了电子转移。在本研究中,通过简单的原位光催化方法合成了负载铂(Pt)、银(Ag)、金(Au)和钯(Pd) NPs的基于等离子体贵金属的卟啉六边形亚微线复合材料(M-HW)。M-HW复合材料上均匀分布的金属颗粒增强了有机功能纳米结构的催化或化学性质。在相同的金属NP负载量下,Ag-HW [k (0.043 min)]复合材料对甲基橙的光催化降解效率是HW的三倍,其次是Pt-HW [k (0.0417 min)]、Au-HW [k (0.0312 min)]和Pd-HW [k (0.0198 min)]。然而,Pt-HW对罗丹明B(RhB)和曙红B的光催化降解分别是HW的4倍和2.6倍。最后,研究了M-HW系统的SPR诱导电子注入、俘获和复合过程。这些结果表明,M-HW等离子体光催化剂表现出优异的光催化性能,使其成为光降解有机污染物的有前途的材料。