Revealing Electron Transfer Dynamics in a ZnIn2S4/PDA S-scheme Photocatalyst via Fs-TAS
Chenrui Hu , Songyu Yang , Bowen He , Bei Cheng , Haiyan Tan , Jianjun Zhang , Jiaguo Yu
Transactions of Tianjin University ›› : 1 -13.
Single-component ZnIn2S4 (ZIS) exhibits rapid charge recombination, resulting in low photocatalytic efficiency. To address this issue, the construction of an S-scheme heterojunction is a feasible strategy. Herein, a ZIS/dopamine (PDA) S-scheme heterojunction photocatalyst was successfully fabricated by depositing PDA onto the surface of ZIS nanoflowers. The optimized ZIS/PDA composite shows a significantly improved H2 production rate compared to pure ZIS and PDA. In situ irradiated X-ray photoelectron spectroscopy provides steady-state spectral evidence of S-scheme electron transfer from ZIS to PDA upon photoexcitation. Furthermore, transient spectral evidence for the ZIS/PDA S-scheme heterojunction is revealed via femtosecond transient absorption spectroscopy. Analysis of the charge dynamics in the ZIS component identifies an additional ultrafast lifetime component in the ZIS/PDA composites. This newly identified component is primarily attributable to the S-scheme interfacial electron transfer channel. The S-scheme electron transfer process gradually accelerates with increasing PDA concentration, ultimately reaching an optimal interfacial electron transfer lifetime of 0.9 ps. This ultrafast electron transfer dynamics facilitates the participation of photogenerated charge carriers in photocatalytic H2 evolution. Overall, this study provides new insights into the transient spectral analysis of S-scheme photocatalysts.
S-scheme heterojunction / Photocatalysis / Transient absorption spectroscopy / Electron transfer dynamics / Interfacial electron transfer
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The Author(s) under exclusive licence to Tianjin University
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