4.7 Article

Selective adsorption of cysteamine molecules on Au/TiO2 boosts visible light-driven photocatalytic hydrogen evolution

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 633, Issue -, Pages 1033-1041

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.12.011

Keywords

Hydrogen evolution reaction; Surface plasmon; Plasmonic nanoparticle; Surface functionalization; Plasmon-molecule interface

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Photocatalytic evolution of hydrogen is an important research area, and the efficiency of visible light-driven photocatalysis can be enhanced by functionalizing Au/TiO2 nanocomposite with cysteamine molecules.
Photocatalytic evolution of hydrogen is becoming a research hotspot because it can help to produce clean energy and reduce environmental pollution. Titanium dioxide (TiO2) and its composites are photocatalysts that are widely used in hydrogen evolution because of their high abundance in nature, low price, and high photo/chemical stability. However, their catalytic performances still need to be further improved, particularly in the visible light spectrum. Herein, visible light-driven photocatalytic evolution of hydrogen on Au/TiO2 nanocomposite is enhanced ti 10 folds by selectively functionalizing the nanocomposite with cysteamine molecules. It is revealed that the amine group (-NH2) in cysteamine favors the transfer and separation of photo-generated hot carriers. The rate of hydrogen produced can be further tuned by varying the ionization of the functionalized molecules at different pH values. This work provides a simple, convenient, and effective method that can be used to improve the photocatalytic evolution of hydrogen. This method can also be used for many other nanocatalysts (e.g., Au-MoS2, AuBiVO4) and catalytic reactions (e.g., carbon dioxide reduction, nitrogen reduction). (c) 2022 Elsevier Inc. All rights reserved.

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