9 research outputs found
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Electronic Tuning of Active Sites in Bifunctional Covalent Organic Frameworks for Photoassisted CO<sub>2</sub> Electrocatalytic Full Reaction
Realizing simultaneously energy-efficiency improvement
and green
economic implementation remains a daunting challenge in addressing
the low-efficiency issues of CO2 electroreduction to meet
the sustainable development strategy. Here, we propose a series of
porphyrin-based COFs (TTCOF-M, M = Co, Ni, and Cu) as model catalysts to study the hybrid CO2 electrocatalytic
full reaction for the first time, during which the catalysts can simultaneously
accomplish photoassisted CO2 electroreduction and 4-nitrophenol
(4-NP) mineralization. As model catalysts, the effects of various
parameters have been intensively studied from typical tandem electro-reactions
to extended photoassisted ones. Specifically, TTCOF-Co can achieve the cathodic reduction efficiency increasing from 90
to 96% (−0.7 V) after illumination and simultaneously 5 times
shortened reaction time with a 4-NP degradation efficiency of ∼99%.
Notably, the 4-NP mineralization rate is calculated to be ∼93.51%
with ∼30.27 mmol/g/h CO2 production rate, and a
rarely investigated mechanism relating to the 4-NP electro-degradation
has been intensively studied
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Interpenetrating 3D Covalent Organic Framework for Selective Stilbene Photoisomerization and Photocyclization
The
selective photoisomerization or photocyclization
of stilbene
to achieve value upgrade is of great significance in industry applications,
yet it remains a challenge to accomplish both of them through a one-pot
photocatalysis strategy under mild conditions. Here, a sevenfold interpenetrating
3D covalent organic framework (TPDT-COF) has been synthesized
through covalent coupling between N,N,N,N-tetrakis(4-aminophenyl)-1,4-benzenediamine
(light absorption and free radical generation) and 5,5′-(2,1,3-benzothiadiazole-4,7-diyl)bis[2-thiophenecarboxaldehyde]
(catalytic center). The thus-obtained sevenfold interpenetrating structure
presents a functional pore channel with a tunable photocatalytic ability
and specific pore confinement effect that can be applied for selective
stilbene photoisomerization and photocyclization. Noteworthily, it
enables photogeneration of cis-stilbene or phenanthrene
with >99% selectivity by simply changing the gas atmosphere under
mild conditions (Ar, SeleCis. > 99%, SelePhen. 2, SeleCis. Phen. > 99%). Theoretical calculations prove that different
gas atmospheres possess varying influences on the energy barriers
of reaction intermediates, and the pore confinement effect plays a
synergistically catalytic role, thus inducing different product generation.
This study might facilitate the exploration of porous crystalline
materials in selective photoisomerization and photocyclization
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn
Modulated Connection Modes of Redox Units in Molecular Junction Covalent Organic Frameworks for Artificial Photosynthetic Overall Reaction
The precise tuning of components, spatial orientations,
or connection
modes for redox units is vital for gaining deep insight into efficient
artificial photosynthetic overall reaction, yet it is still hard achieve
for heterojunction photocatalysts. Here, we have developed a series
of redox molecular junction covalent organic frameworks (COFs) (M-TTCOF-Zn, M = Bi, Tri, and Tetra) for artificial photosynthetic
overall reaction. The covalent connection between TAPP-Zn and multidentate
TTF endows various connection modes between water photo-oxidation
(multidentate TTF) and CO2 photoreduction (TAPP-Zn) centers
that can serve as desired platforms to study the possible interactions
between redox centers. Notably, Bi-TTCOF-Zn exhibits
a high CO production rate of 11.56 μmol g–1 h–1 (selectivity, ∼100%), which is more
than 2 and 6 times higher than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn, respectively. As revealed by theoretical calculations, Bi-TTCOF-Zn facilitates a more uniform distribution of energy-level
orbitals, faster charge transfer, and stronger *OH adsorption/stabilization
ability than those of Tri-TTCOF-Zn and Tetra-TTCOF-Zn