4.8 Article

Rational design of isostructural 2D porphyrin-based covalent organic frameworks for tunable photocatalytic hydrogen evolution

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-021-21527-3

Keywords

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Funding

  1. National Natural Science Foundation of China [21971251, 21572170, 21772149, 21975188]
  2. Fundamental Research Funds for Central Universities [2042020kf0213]
  3. National Key Research and Development Program of China [2017YFB0702100, 2017YFA0206903]

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Covalent organic frameworks show promise in photocatalytic hydrogen generation from water, with the incorporation of different transition metals allowing for tuning of the hydrogen evolution rate.
Covalent organic frameworks have recently gained increasing attention in photocatalytic hydrogen generation from water. However, their structure-property-activity relationship, which should be beneficial for the structural design, is still far-away explored. Herein, we report the designed synthesis of four isostructural porphyrinic two-dimensional covalent organic frameworks (MPor-DETH-COF, M=H-2, Co, Ni, Zn) and their photocatalytic activity in hydrogen generation. Our results clearly show that all four covalent organic frameworks adopt AA stacking structures, with high crystallinity and large surface area. Interestingly, the incorporation of different transition metals into the porphyrin rings can rationally tune the photocatalytic hydrogen evolution rate of corresponding covalent organic frameworks, with the order of CoPor-DETH-COF

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