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N-Promoted Ru1/TiO2 single-atom catalysts for photocatalytic water splitting for hydrogen production: a density functional theory study

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Abstract

We propose a universal dimer-doping strategy to improve the photocatalytic water splitting activity of Ru1/TiO2 single-atom catalysts, in which the N atom is simultaneously doped. First-principles calculations show that the N dopants promote the substitution of Ti with Ru on the anatase TiO2(101) surface by chemical bonding between Ru and N, and increase the stability of the system. Isolated Ru1 atoms act as active sites for the reduction of protons, and Ru1–N1/TiO2 has a hydrogen evolution activity comparable to that of Pd. The impurity bands within the band gap lead to a significant red-shift of the absorption edge towards the visible region, improving the photoabsorption and photocatalytic performance of TiO2 under sunlight. The reason is the charge compensation effect localized to the doped Ru–N dimers. We expect that this generic scheme that simultaneously realizes band-structure tailoring and reaction control also applies to other single-atom loaded oxide-based photocatalytic systems.

Graphical abstract: N-Promoted Ru1/TiO2 single-atom catalysts for photocatalytic water splitting for hydrogen production: a density functional theory study

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Supplementary files

Article information


Submitted
19 Feb 2020
Accepted
14 Apr 2020
First published
14 Apr 2020

Phys. Chem. Chem. Phys., 2020, Advance Article
Article type
Paper

N-Promoted Ru1/TiO2 single-atom catalysts for photocatalytic water splitting for hydrogen production: a density functional theory study

Z. Luo, Z. Wang, J. Li, K. Yang and G. Zhou, Phys. Chem. Chem. Phys., 2020, Advance Article , DOI: 10.1039/D0CP00929F

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