Releasing Au Electrons to Mo Site for Weakened Mo<i>─</i>H Bond of Mo<sub>2</sub>C MXene Cocatalyst Toward Improved Photocatalytic H<sub>2</sub> Production

Mo<sub>2</sub>C MXene (Mo<sub>2</sub>CT<sub>x</sub>) is one of the most promising noble-metal-free cocatalysts for photocatalytic H<sub>2</sub> production because of its excellent electron transport capacity and abundant Mo sites. However, Mo<sub>2</sub>CT<sub>x</sub> typically exhibits a strong Mo─H<sub>ads</sub> bond, resulting in that the produced H<sub>2</sub> difficultly desorbs from the Mo surface for the limited activity. To effectively weaken the Mo─H<sub>ads</sub> bond, in this paper, a regulation strategy of electron donor Au releasing electrons to the d-orbitals of Mo sites in Mo<sub>2</sub>CT<sub>x</sub> is proposed. Herein, the Mo<sub>2</sub>CT<sub>x</sub>-Au/CdS photocatalysts are prepared through a two-step process, including the initial loading of Au nanoparticles on the Mo<sub>2</sub>CT<sub>x</sub> surface and the subsequent in situ growth of CdS onto the Mo<sub>2</sub>CT<sub>x</sub>-Au surface. Photocatalytic measurements indicate that the maximal H<sub>2</sub>-production rate of Mo<sub>2</sub>CT<sub>x</sub>-Au/CdS reaches up to 2799.44 µmol g<sup>-1</sup> h<sup>-1</sup>, which is 30.99 and 3.60 times higher than that of CdS and Mo<sub>2</sub>CT<sub>x</sub>/CdS, respectively. Experimental and theoretical data corroborate that metallic Au can transfer free electrons to Mo<sub>2</sub>CT<sub>x</sub> to generate electron-enriched Mo<sup>δ-</sup> sites, thus causing the increased antibonding-orbital occupancy state and the weakened Mo─H<sub>ads</sub> bond for the boosted H<sub>2</sub>-production efficiency. This research provides a promising approach for designing Mo<sub>2</sub>CT<sub>x</sub>-based cocatalysts by regulating the antibonding-orbital occupancy of Mo sites for improved photocatalytic performance.

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Publication Details

Journal
Small
Published
2024-08-30
DOI
https://doi.org/10.1002/smll.202405378
Citations
19
Primary Topic
MXene and MAX Phase Materials
Type
article
Field-Weighted Citation Impact
2.23

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article

Releasing Au Electrons to Mo Site for Weakened Mo─H Bond of Mo2C MXene Cocatalyst Toward Improved Photocatalytic H2 Production

Huogen Yu, Xiaochun Ke, Xuefei Wang, Ping Wang et al.
19 citations
Small
MXene and MAX Phase Materials
2.23
article

Releasing Au Electrons to Mo Site for Weakened Mo─H Bond of Mo2C MXene Cocatalyst Toward Improved Photocatalytic H2 Production

Huogen Yu, Xiaochun Ke, Xuefei Wang, Ping Wang, Feng Chen
article en
19 citations

Abstract

Mo<sub>2</sub>C MXene (Mo<sub>2</sub>CT<sub>x</sub>) is one of the most promising noble-metal-free cocatalysts for photocatalytic H<sub>2</sub> production because of its excellent electron transport capacity and abundant Mo sites. However, Mo<sub>2</sub>CT<sub>x</sub> typically exhibits a strong Mo─H<sub>ads</sub> bond, resulting in that the produced H<sub>2</sub> difficultly desorbs from the Mo surface for the limited activity. To effectively weaken the Mo─H<sub>ads</sub> bond, in this paper, a regulation strategy of electron donor Au releasing electrons to the d-orbitals of Mo sites in Mo<sub>2</sub>CT<sub>x</sub> is proposed. Herein, the Mo<sub>2</sub>CT<sub>x</sub>-Au/CdS photocatalysts are prepared through a two-step process, including the initial loading of Au nanoparticles on the Mo<sub>2</sub>CT<sub>x</sub> surface and the subsequent in situ growth of CdS onto the Mo<sub>2</sub>CT<sub>x</sub>-Au surface. Photocatalytic measurements indicate that the maximal H<sub>2</sub>-production rate of Mo<sub>2</sub>CT<sub>x</sub>-Au/CdS reaches up to 2799.44 µmol g<sup>-1</sup> h<sup>-1</sup>, which is 30.99 and 3.60 times higher than that of CdS and Mo<sub>2</sub>CT<sub>x</sub>/CdS, respectively. Experimental and theoretical data corroborate that metallic Au can transfer free electrons to Mo<sub>2</sub>CT<sub>x</sub> to generate electron-enriched Mo<sup>δ-</sup> sites, thus causing the increased antibonding-orbital occupancy state and the weakened Mo─H<sub>ads</sub> bond for the boosted H<sub>2</sub>-production efficiency. This research provides a promising approach for designing Mo<sub>2</sub>CT<sub>x</sub>-based cocatalysts by regulating the antibonding-orbital occupancy of Mo sites for improved photocatalytic performance.

SmallVol. 20(48)
Wuhan University of Technology (CN), China University of Geosciences (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province
Openalex Percentile: Top 8%
MXene and MAX Phase Materials
2.23
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