A first
example of an sp2 carbon-conjugated three-dimensional
(3D) covalent organic framework (COF) (BUCT-COF-4) is synthesized
via the Knoevenagel condensation of the saddle-shaped aldehyde-substituted
cyclooctatetrathiophene and 1,4-phenylenediacetonitrile. Ascribed
to the extended π-conjugation and long-range ordered structures,
BUCT-COF-4 displays high Hall electron mobility of 1.97 cm2 V–1 s–1 at room temperature.
After it is doped with iodine, the material not only exhibits an enhanced
electron mobility up to 2.62 cm2 V–1 s–1 in ambient air but also presents an unexpected metal-free
ferromagnetic phase transition arising from the formation of aligned
spins unidirectional across the whole sp2 carbon-conjugated
3D framework. This is the first report of a ferromagnetic phenomenon
in 3D COF materials, which would broaden promising applications and
open a new frontier in COF materials.
Lanthanide-based luminescent sensors have been widely used for the detection of the anthrax biomarker dipicolinic acid (DPA). However, mainly based on DPA sensitization to the lanthanide core, most of them failed to realize robust detection of DPA in bacterial spores. We proposed a new strategy for reliable detection of DPA by perturbing a tandem energy transfer in heterobinuclear lanthanide coordination polymer nanoparticles simply constructed by two kinds of lanthanide ions, Tb and Eu, and guanosine 5'-monophosphate. This smart luminescent probe was demonstrated to exhibit highly sensitive and selective visual luminescence color change upon exposure to DPA, enabling accurate detection of DPA in complex biosystems such as bacterial spores. DPA release from bacterial spores on physiological germination was also successfully monitored in real time by confocal imaging. This probe is thus expected to be a powerful tool for efficient detection of bacterial spores in responding to anthrax threats.
The application of three-dimensional (3D) covalent organic frameworks (COFs) in renewable energy fields is greatly limited due to their nonconjugated skeletons. Here, we design and successfully synthesize a thiophene-enriched fully conjugated 3D COF (BUCT-COF-11) through an all-thiophene-linked saddle-shaped building block (COThTh-CHO). The BUCT-COF-11 exhibits excellent semiconducting property with intrinsic metal-free oxygen reduction reaction (ORR) activity. Using the COF as cathode catalyst, the assembled anion-exchange membrane fuel cells (AEMFCs) exhibited a high peak power density up to 493 mW cm À 2 . DFT calculations reveal that thiophene introduction in the COF not only improves the conductivity but also optimizes the electronic structure of the sample, which therefore boosts the ORR performance. This is the first report on the application of COFs as metal-free catalysts in fuel cells, demonstrating the great potential of fully conjugated 3D COFs as promising semiconductors in energy fields.
The application of three‐dimensional (3D) covalent organic frameworks (COFs) in renewable energy fields is greatly limited due to their non‐conjugated skeletons. Here, we design and successfully synthesize a thiophene‐enriched fully conjugated 3D COF (BUCT‐COF‐11) through an all‐thiophene‐linked saddle‐shaped building block (COThTh‐CHO). The BUCT‐COF‐11 exhibits excellent semiconducting property with intrinsic metal‐free oxygen reduction reaction (ORR) activity. Using the COF as cathode catalyst, the assembled anion‐exchange membrane fuel cells (AEMFCs) exhibited a high peak power density up to 493 mW cm−2. DFT calculations reveal that thiophene introduction in the COF not only improves the conductivity but also optimizes the electronic structure of the sample, which therefore boosts the ORR performance. This is the first report on the application of COFs as metal‐free catalysts in fuel cells, demonstrating the great potential of fully conjugated 3D COFs as promising semiconductors in energy fields.
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