Species heterogeneity and synergy to boost photocatalytic hydrogen evolution

Zhang, Jiankang, Qiao, Panzhe, Tan, Hao, Cui, Lin, Zhou, Zhan, Lin, Dong, Tuo, Yongxiao and Qin, Yong 2024. Species heterogeneity and synergy to boost photocatalytic hydrogen evolution. ACS Catalysis 14 (20) , pp. 15699-15712. 10.1021/acscatal.4c03593 Item availability restricted.

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Abstract

Integrating different reaction sites, such as single atom (SA), nanocluster (NC), and oxygen vacancy (Ov), in a specific photocatalyst affords a new prospect to break through the limitations of SA catalysis. However, the intrinsic influence mechanisms of cocatalyst size and Ov on the photocatalytic performance and synergy are still not well unraveled. Herein, we report the synthesis and investigation of atomically dispersed Pt-based photocatalysts surface-confined in Ov-containing porous TiO2 nanoflowers via atomic layer deposition. The SA–NC coexisting PtSA+NC@TiO2 photocatalysts exhibit optimized hydrogen evolution activity (2260 h–1), which is 3.6-fold higher than that of PtSA@TiO2 counterparts. Moreover, the activity can be further remarkably enhanced to 3645 h–1 by engineering the cocatalyst size and Ov concentration. We identify the ad-/desorption sites of the reacting molecules and unravel the synergistic catalytic mechanisms of the active speciesthrough characterizations and density functional theory calculations: Pt NC is responsible for the adsorption–dissociation of H2O molecules preferentially adsorbed on Ti sites and meanwhile lowers the d-band center of Pt SA responsible for the desorption of H2 molecules, and the adjacent Ov can stabilize the cocatalysts and modify the electronic energy distribution of Pt NC, achieving the optimized adsorption state toward the *OH intermediate. The present multiple-site engineering concept and mechanistic insights are expected to shed light on the rational design of atomically dispersed photocatalysts.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Publisher:	American Chemical Society
ISSN:	2155-5435
Date of First Compliant Deposit:	13 November 2024
Date of Acceptance:	27 September 2024
Last Modified:	13 Nov 2024 10:00
URI:	https://orca.cardiff.ac.uk/id/eprint/172981

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