Experimental Identification of Ultrafast Reverse Hole Transfer at the Interface of the Photoexcited Methanol/Graphitic Carbon Nitride System

被引:100
作者
Chen, Zongwei [1 ]
Zhang, Qun [1 ]
Luo, Yi [1 ]
机构
[1] Univ Sci & Technol China, Synerget Innovat Ctr Quantum Informat & Quantum P, Dept Chem Phys, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
关键词
hole scavenging; methanol; photocatalysis; photoexcited hole dynamics; ultrafast transient absorption spectroscopy; ELECTRON-TRANSFER; LEVEL ALIGNMENT; TRAPPED HOLES; METHANOL; HYDROGEN; TIO2; DYNAMICS; FORMALDEHYDE; SURFACE;
D O I
10.1002/anie.201713102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An experimental scrutiny of the photoexcited hole dynamics in a prototypical system is presented in which hole-scavenging methanol molecules are chemisorbed on a graphitic carbon nitride (g-C3N4) substrate. A set of comparison and control experiments by means of femtosecond time-resolved transient absorption (fs-TA) spectroscopy were conducted. The elusive reverse hole transfer (RHT) process was identified, which occurs on a timescale of a few hundred picoseconds. The critical role of interfacially chemisorbed methoxy (instead of methanol) as the dominant species responsible for hole scavenging was confirmed by a control experiment using protonated g-C3N4 as the substrate. A hot-hole transfer effect was revealed by implementing different interband photoexcitation scenarios. The RHT rate is the key factor governing the hole-scavenging ability of different hole scavengers.
引用
收藏
页码:5320 / 5324
页数:5
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