Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction: Difference between revisions

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DOI 10.1039/d0cc05047d
Authors Yanan Wang, Xue-Wang Gao, Junli Li, Duobin Chao,
Submitted 03.09.2020
Published online 2020
Licenses http://rsc.li/journals-terms-of-use,
Subjects -
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In this study, the experiments were done with the sacrificial electron donor TEA ({{#moleculelink:|link=ZMANZCXQSJIPKH-UHFFFAOYSA-N|image=false|width=300|height=200}}).
In this study, the experiments were done with the sacrificial electron donor TEA ({{#moleculelink:|link=ZMANZCXQSJIPKH-UHFFFAOYSA-N|image=false|width=300|height=200}}).
====Additives====
====Additives====
In this study, no additives were tested. Control experiments with other photosensitizers (Ru(bpy)<sub>3</sub>, Fluorescein and Eosin Y) and catalysts (FeCl3) were conducted.
In this study, no additives were tested. Control experiments with other photosensitizers (Ru(bpy)<sub>3</sub>, Fluorescein and Eosin Y) and catalysts (FeCl<sub>3</sub>) were conducted.

Latest revision as of 12:14, 16 May 2024


Abstract[edit | edit source]

Summary[edit | edit source]

The photochemical reduction of CO2 to CO was shown using the iron complex Fe(tpy-tol)Cl3 in combination with the organic photosensitizer 4CzIPN. Turnover numbers (TONs) of up to 2250 and a selectivity of 99.3% for CO were reached in DMF/H2O. The experiments were conducted under visible-light irradiation (λ > 420 nm) with TEA (see section SEDs below) as sacrificial electron donor.

Advances and special progress[edit | edit source]

The presented study contains the first example for the use of an organic thermally activated delayed fluorescence (TADF) compound as a photosensitizer in CO2 reduction.

Additional remarks[edit | edit source]

Content of the published article in detail[edit | edit source]

The article contains results of a study for the reduction of CO2 to CO using an iron complex and an organic TADF photosensitizer. The catalytic system performs best (referring to the TON of CO production) in DMF.

Catalyst[edit | edit source]

Fe(tpy-tol)Cl3

Photosensitizer[edit | edit source]

4CzIPN

Investigation[edit | edit source]

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent A...λexc [nm].TON CO.
1.

Fe(tpy-tol)Cl3

0.01

4CzIPN

0.05

TEA

0.28

DMF

420-6502250
2.

Fe(tpy-tol)Cl3

0.01

4CzIPN

0.01

TEA

0.28

DMF

420-650133
3.

Fe(tpy-tol)Cl3

0.01

4CzIPN

0.05

TEA

0.28

DMF

420-650244
4.

Fe(tpy-tol)Cl3

0.01

4CzIPN

0.1

TEA

0.28

DMF

420-650246
5.

Fe(tpy-tol)Cl3

0.01

FeCl3

0.05

TEA

0.28

DMF

420-6506
6.

Ru(bpy)3

0.01

4CzIPN

0.05

TEA

0.28

DMF

420-65017
7.

Molecule:100955

0.01

4CzIPN

0.05

TEA

0.28

DMF

420-6500
8.

Eosin Y

0.01

4CzIPN

0.05

TEA

0.28

DMF

420-6500
Investigation-Name: photocatalytic reduction of CO2 to CO

Sacrificial electron donor[edit | edit source]

In this study, the experiments were done with the sacrificial electron donor TEA (TEA).

Additives[edit | edit source]

In this study, no additives were tested. Control experiments with other photosensitizers (Ru(bpy)3, Fluorescein and Eosin Y) and catalysts (FeCl3) were conducted.

Investigations