Controlled synthesis of 2D-2D conductive metal-organic framework/g-CN heterojunctions for efficient photocatalytic hydrogen evolution
Designing photocatalysts with efficient charge separation and electron transport capabilities to achieve efficient visible-driven hydrogen production remains a challenge. Herein, 2D-2D conductive metal-organic framework/g-C 3 N 4 heterojunctions were successfully prepared by an in situ assembly. Com...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2024-02, Vol.53 (6), p.2534-254 |
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Zusammenfassung: | Designing photocatalysts with efficient charge separation and electron transport capabilities to achieve efficient visible-driven hydrogen production remains a challenge. Herein, 2D-2D conductive metal-organic framework/g-C
3
N
4
heterojunctions were successfully prepared by an
in situ
assembly. Compared to pristine g-C
3
N
4
, the ratio-optimized Ni-CAT-1/g-C
3
N
4
exhibits approximately 3.6 times higher visible-light H
2
production activity, reaching 14 mmol g
−1
. Through investigations using time-resolved photoluminescence, surface photovoltage, and wavelength-dependent photocurrent action spectroscopies, it is determined that the improved photocatalytic performance is attributed to enhanced charge transfer and separation, specifically the efficient transfer of excited high-energy-level electrons from g-C
3
N
4
to Ni-CAT in the heterojunctions. Furthermore, the high electrical conductivity of Ni-CAT enables rapid electron transport, contributing to the overall enhanced performance. This work provides a feasible strategy to construct efficient dimension-matched g-C
3
N
4
-based heterojunction photocatalysts with high-efficiency charge separation for solar-driven H
2
production.
Dimension-matched Ni-CAT-1/g-C
3
N
4
heterojunctions are synthesized with exceptional visible-light photoactivity for hydrogen evolution. The high electrical conductivity of Ni-CAT-1 enables rapid electron transport and facilitates charge separation. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/d3dt03894g |