A novel BODIPY-based MOF photocatalyst for efficient visible-light-driven hydrogen evolution
Considerable attention has been paid to promising applications of photoactive metal-organic frameworks (MOFs) in visible-light-enhanced hydrogen production. In this study, a pillared-paddlewheel type metal-organic framework [Zn 2 (BODIPY)(BPDC) 2 ]·H 2 O (denoted as CCNU-1) featuring BODIPY struts,...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (17), p.1439-1445 |
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Sprache: | eng |
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Zusammenfassung: | Considerable attention has been paid to promising applications of photoactive metal-organic frameworks (MOFs) in visible-light-enhanced hydrogen production. In this study, a pillared-paddlewheel type metal-organic framework [Zn
2
(BODIPY)(BPDC)
2
]·H
2
O (denoted as CCNU-1) featuring BODIPY struts, and capable of efficiently absorbing visible light from 200 to 800 nm, has been fabricated, which is thought to be the first BODIPY-based MOF decorated with Pt nanoparticles as the co-catalyst for efficient photocatalytic H
2
generation under visible-light illumination. Impressively, Pt/CCNU-1 exhibited a remarkable H
2
production rate as high as 4680 μmol g
−1
h
−1
with the use of
l
-ascorbic acid as a sacrificial reagent from an aqueous medium, and a high apparent quantum efficiency of 9.06% at 420 nm. To our knowledge, Pt/CCNU-1 is the most visible-light photoactive Pt/MOF composite for H
2
generation from water hitherto, highlighting the promising future of MOF materials in solar-to-chemical energy conversion. This work provides significant insights into the development of MOF-based systems for visible-light-responsive photocatalysts for water reduction.
The first BODIPY-based MOF decorated with a Pt co-catalyst exhibited efficient photocatalytic H
2
evolution under visible-light illumination, representing the most visible-light photoactive MOF material for H
2
evolution from water thus far. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c9ta02357g |