Investigation of the local photothermal effects by fabricating a CQDs/Au/TiO2 photoelectrode in a PEC water splitting system. Issue 6 (4th February 2022)

• Record Type: Journal Article
• Authors: Cao, Angran; Sang, Lixia; Yu, Zexin; Zhao, Yue; Wang, Xudong; Wang, Chong; Ma, Mengnan
• Is Part Of: Catalysis science & technology. Volume 12:Issue 6(2022)
• Page Start: 1859
• Page End: 1868
• Publication Date: 2022-02-04
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/d1cy02113c
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Au nanoparticles (Au NPs) and carbon quantum dots (CQDs) have been proved to generate strong local photothermal effects in a PEC water splitting system. Abstract : The high efficiency of the photoanode material is of great significance for photoelectrochemical (PEC) water splitting. Herein, a CQDs/Au/TiO2 nanorod array composite photoanode was constructed with special attention to local photothermal effects. The intensity and characteristics of the local thermal effect generated by the photothermal conversion of plasmonic Au nanoparticles (Au NPs) and carbon quantum dots (CQDs) are accurately represented by an equivalent simplified temperature field model constructed innovatively. Further studies demonstrated that the local thermal effect not only stimulates the activity of the small polaron semiconductor TiO2, but also accelerates the charge transfer and surface dynamic reaction from the aspects of kinetics and thermodynamics. Simulation and experimental results also showed that the surface plasmon resonance (SPR) effect of Au NPs and the up-conversion fluorescence characteristics of CQDs can cooperate to improve the carrier concentration. Meanwhile, the formation of a Schottky heterojunction between Au and TiO2, and CQDs as hole collectors synergistically promoted the bulk charge separation. Therefore, the CQDs/Au/TiO2 photoanode achieved a remarkable H2 evolution rate of 641.9 μL h −1 cm −2 under AM 1.5 illumination, five times higher than that of the pure TiO2 photoanode.