4.7 Article

Constructing tightly integrated conductive metal-organic framework/covalent triazine framework heterostructure by coordination bonds for photocatalytic hydrogen evolution

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 633, Issue -, Pages 233-242

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.11.094

Keywords

Covalent triazine frameworks; Conductive MOF; Photocatalytic hydrogen evolution; Charge separation; Z-Scheme heterostructure

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Through a novel coordinating connection mode, a covalent triazine framework (CTF-1) is tightly integrated with a conductive two-dimensional metal-organic framework (Ni-CAT-1), resulting in significantly enhanced visible-light-driven hydrogen evolution. The conductive 2D Ni-CAT-1 effectively facilitates the separation of photogenerated carriers and leads to a remarkable improvement in photocatalytic hydrogen evolution activity. This work provides a novel strategy for constructing tightly integrated MOF/COF hybrid materials.
The construction of tightly integrated heterostructures with metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) has been confirmed to be an effective way for improved hydrogen evolution. However, the reported tightly integrated MOF/COF hybrids were usually limited to the cova-lent connection of COFs with aldehyde groups and NH2-MOF via Schiff base reaction, restricting the development of MOF/COF hybrids. Herein, a covalent triazine framework (CTF-1), a subtype of crystalline COFs, was integrated with a conductive two-dimensional (2D) MOF (Ni-CAT-1) by a novel coordinating connection mode for significantly enhanced visible-light-driven hydrogen evolution. The terminal ami-dine groups in the CTF-1 layers offer dual N sites for the coordination of metal ions, which provides the potential of coordinating connection between CTF-1 and Ni-CAT-1. The conductive 2D Ni-CAT-1 in Ni-CAT-1/CTF-1 hybrids effectively facilitates the separation of photogenerated carriers of CTF-1 compo-nent, and the resultant hybrid materials show significantly enhanced photocatalytic hydrogen evolution activity. In particular, the Ni-CAT-1/CTF-1 (1:19) sample exhibits the maximum hydrogen evolution rate of 8.03 mmol g-1h-1, which is about four times higher than that of the parent CTF-1 (1.96 mmol g-1h-1). The enhanced photocatalytic activity of Ni-CAT-1/CTF-1 is mainly attributed to the incorporation of con-ductive MOF which leads to the formation of a Z-Scheme heterostructure, promoting the electron transfer in hybrid materials. The coordinating combination mode of Ni-CAT-1 and CTF-1 in this work provides a novel strategy for constructing tightly integrated MOF/COF hybrid materials.(c) 2022 Elsevier Inc. All rights reserved.

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