Volume 57, Issue 19
Communication

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

Zongwei Chen

Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui, 230026 China

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Prof. Dr. Qun Zhang

Corresponding Author

Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui, 230026 China

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Prof. Dr. Yi Luo

Corresponding Author

Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui, 230026 China

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First published: 08 March 2018
Citations: 28

Abstract

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.

Number of times cited according to CrossRef: 28

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