Department of Chemistry & Pharmacy and Interdisciplinary Center for Molecular Materials, Friedrich Alexander University Erlangen-Nuremberg, Egerlandstrasse 3, 91058 Erlangen, Germany.
Nanoscale. 2017 Jun 14;9(23):7911-7921. doi: 10.1039/c7nr00759k.
A new insight into photoinduced charge transfer processes across carbon nanotube@TiO interfaces has been gained based on experimental details from transient absorption spectroscopy. We show that photoinduced, interfacial hole transfer to carboxylic acid-functionalized multiwalled carbon nanotubes (oxMWCNTs) from TiO results in hole-doped oxMWCNTs and reduced TiO. The latter is inferred from femto- and nanosecond transient absorption spectroscopy performed with oxMWCNT@TiO dispersions and complemented with investigations using methyl viologen and N,N,N',N'-tetramethyl-p-phenylenediamine as an electron scavenger and a hole scavenger, respectively. The results of ultraviolet photoemission spectroscopy (UPS) of the compounds corroborate the findings, highlighting the strong coupling between oxMWCNTs and TiO in these hybrids.
基于瞬态吸收光谱的实验细节,我们对碳纳米管@TiO 界面上光诱导电荷转移过程有了新的认识。我们表明,从 TiO 到羧酸功能化多壁碳纳米管(oxMWCNTs)的光诱导界面空穴转移导致空穴掺杂的 oxMWCNTs 和还原的 TiO。后者是通过 oxMWCNT@TiO 分散体进行的飞秒和纳秒瞬态吸收光谱推断出来的,并辅以使用甲基紫精和 N,N,N',N'-四甲基对苯二胺分别作为电子捕获剂和空穴捕获剂的研究。这些化合物的紫外光电子能谱(UPS)的结果证实了这一发现,突出了这些杂化物中 oxMWCNTs 和 TiO 之间的强耦合。