F− surface modified ZnO for enhanced photocatalytic H2O2 production and its fs-TAS investigation
Year: 2024
Type: article
Abstract: Pure ZnO exhibits low photocatalytic H 2 O 2 production activity due to the rapid charge recombination. To realize the spatial separation of photogenerated electrons and holes, constructing an electron transfer channel on the ZnO surface is an effective approach. This study successfully modified the surface of ZnO using F − (ZnO/F) by introducing NH 4 F in an aqueous phase photocatalytic system. The F − is adsorbed on the ZnO surface by Coulombic force and significantly improves the photocatalytic H 2 O 2 production performance of ZnO, with the highest efficiency of 4137.2 μmol⋅g −1 ·L −1 ·h – 1 . The photocatalytic performance enhancement mechanism of ZnO/F is explained in terms of electron transfer dynamics by femtosecond transient absorption spectroscopy (fs-TAS) measurements. F − surface modification constructs a new ultrafast electron transport pathway from the ZnO CB to F − , and the optimal ZnO/F exhibits the fastest interfacial electron transfer lifetime of 5.8 ps. The F − surface modification effectively facilitates the charge separation, thereby increasing the number of electrons available for photocatalytic H 2 O 2 reaction. This study has revealed the roles of F − surface modification in the photocatalytic H 2 O 2 production by ZnO and provides guidance for ionic modification to improve photocatalytic performance. • The optimal F − modified ZnO achieves a H 2 O 2 production rate of 4137.2 μmol⋅g −1 ⋅L −1 ⋅h −1 . • F − effectively facilitates the separation and transfer of electrons in ZnO. • Interfacial electron transfer dynamics of F − modified ZnO is revealed by femtosecond transient absorption spectroscopy. • F − is adsorbed on the ZnO surface by Coulombic force.
Source: Journal of Materiomics
Authors: Xin Zhou, Chenbin Ai, Xiaojing Wang, Zhen Wu, Jianjun Zhang
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,750
OpenAlex ID: W4404538266
