Encapsulating fullerene into Ti-based metal-organic frameworks with anchored atomically dispersed Pt cocatalysts for efficient hydrogen evolution.

J Colloid Interface Sci

School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, China; South China University of Technology-Zhuhai Institute of Modern Industrial Innovation, Zhuhai 519175, China. Electronic address:

Published: November 2024

Ti-based Metal-organic frameworks (Ti-MOF) have been extensively investigated for producing hydrogen via solar water splitting, while their intrinsic activities are still retarded by the poor performance of photocarriers separation and utilization. Herein, a donor-acceptor (D-A) supramolecular photocatalyst is successfully constructed via encapsulating fullerene (C) into MIL-125-NH and meanwhile depositing individual Pt atoms as cocatalyst. The as-prepared C@MIL-125-NH-Pt exhibits remarkable activity in photocatalytic water splitting, with a H formation rate of 1180 μmol g h, which is ∼ 12 times higher than that of the pristine MIL-125-NH. Further investigations indicate that the host-guest interactions between C and MIL-125-NH strengthen the built-in electric field, which greatly facilitates the separation and migration of photogenerated charge carriers. In addition, the cocatalyst of individual Pt atoms not only further promotes the separation and transport of carriers but also enhances the contact between water and the catalyst. All of these factors directly contribute to the superior activity of C@MIL-125-NH-Pt. This work provides a new perspective for constructing D-A supramolecular photocatalysts for enhanced charge separation and making full use of photoelectrons to realize efficient hydrogen production.

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Source
http://dx.doi.org/10.1016/j.jcis.2024.06.077DOI Listing

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