Visible-Light Photocatalytic Conversion of Carbon Dioxide by Ni(II) Complexes with N4S2 Coordination: Highly Efficient and Selective Production of Formate: Difference between revisions

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DOI 10.1021/jacs.0c08145
Authors Sung Eun Lee, Azam Nasirian, Ye Eun Kim, Pegah Tavakoli Fard, Youngmee Kim, Byeongmoon Jeong, Sung-Jin Kim, Jin-Ook Baeg, Jinheung Kim,
Submitted 19.10.2020
Published online 19.10.2020
Licenses https://doi.org/10.15223/policy-029, https://doi.org/10.15223/policy-037, https://doi.org/10.15223/policy-045,
Subjects Colloid and Surface Chemistry, Biochemistry, General Chemistry, Catalysis
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{{#doiinfobox: 10.1021/jacs.0c08145}}
{{DOI|doi=10.1021/jacs.0c08145}}
===Abstract===
===Abstract===
====Summary====
====Summary====
A photochemical reduction of CO<sub>2</sub> to formate was shown using the nickel complexes {{#moleculelink:|link=CLQAFMRCKIGWOF-UHFFFAOYSA-L|image=false|width=300|height=200}} or {{#moleculelink:|link=BDPUYSVREMMVBP-UHFFFAOYSA-L|image=false|width=300|height=200}} as catalysts in combination with the organic photosensitizer {{#moleculelink:|link=SEACYXSIPDVVMV-UHFFFAOYSA-L|image=false|width=300|height=200}}. Turnover numbers (TONs) of  up to 14000 and a selectivity of >99% for formate were reached in ethanol/water. The experiments were conducted under visible-light irradiation (λ > 400 nm) using TEOA as sacrificial electron donor (see section SEDs below).
A photochemical reduction of CO<sub>2</sub> to formate was shown using the nickel complexes {{#moleculelink:|link=CLQAFMRCKIGWOF-UHFFFAOYSA-L|image=false|width=300|height=200}} or {{#moleculelink:|link=BDPUYSVREMMVBP-UHFFFAOYSA-L|image=false|width=300|height=200}} as catalysts in combination with the organic photosensitizer {{#moleculelink:|link=SEACYXSIPDVVMV-UHFFFAOYSA-L|image=false|width=300|height=200}}. Turnover numbers (TONs) of  up to 14000 and a selectivity of >99% for formate were reached in ethanol/water. The experiments were conducted under visible-light irradiation (λ > 400 nm) using TEOA as sacrificial electron donor (see section SEDs below).
====Advances and special progress====
====Advances and special progress====
A set of novel nickel complexes have been developed and shown to possess remarkably high efficiencies as catalysts in CO<sub>2</sub> reduction.
A set of bioinspired nickel complexes have been developed and shown to possess remarkably high efficiencies and selectivities as catalysts in CO<sub>2</sub> reduction, being the (at that time) best early transition metal complexes for photocatalytic CO<sub>2</sub> conversion.


====Additional remarks====
====Additional remarks====
The nickel complexes were also active catalysts for hydrogen photoreduction under argon atmosphere.
===Content of the published article in detail===
===Content of the published article in detail===
The article contains results for the reduction of CO<sub>2</sub> to formate under visible-light catalysis using nickel complexes and an organic photosensitizer. The catalytic system performs best (referring to the TON of formate production) in ethanol/water with complex {{#moleculelink:|link=CLQAFMRCKIGWOF-UHFFFAOYSA-L|image=false|width=300|height=200}} as a catalyst.
The article contains results for the reduction of CO<sub>2</sub> to formate under visible-light catalysis using nickel complexes and an organic photosensitizer. The catalytic system performs best (referring to the TON of formate production) in ethanol/water with complex {{#moleculelink:|link=CLQAFMRCKIGWOF-UHFFFAOYSA-L|image=false|width=300|height=200}} as a catalyst.
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==== Additives ====
==== Additives ====
In this study, different additives were used.  
In this study, no additives were tested.  
[[Category:Photocatalytic CO2 conversion to HCOOH]]
[[Category:Photocatalytic CO2 conversion to HCOOH]][[Category:Publication]]

Latest revision as of 10:37, 11 April 2024


Abstract[edit | edit source]

Summary[edit | edit source]

A photochemical reduction of CO2 to formate was shown using the nickel complexes Ni(pbi)(pyS)2 or Ni(pbt)(pyS)2 as catalysts in combination with the organic photosensitizer Eosin Y. Turnover numbers (TONs) of up to 14000 and a selectivity of >99% for formate were reached in ethanol/water. The experiments were conducted under visible-light irradiation (λ > 400 nm) using TEOA as sacrificial electron donor (see section SEDs below).

Advances and special progress[edit | edit source]

A set of bioinspired nickel complexes have been developed and shown to possess remarkably high efficiencies and selectivities as catalysts in CO2 reduction, being the (at that time) best early transition metal complexes for photocatalytic CO2 conversion.

Additional remarks[edit | edit source]

The nickel complexes were also active catalysts for hydrogen photoreduction under argon atmosphere.

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

The article contains results for the reduction of CO2 to formate under visible-light catalysis using nickel complexes and an organic photosensitizer. The catalytic system performs best (referring to the TON of formate production) in ethanol/water with complex Ni(pbi)(pyS)2 as a catalyst.

Catalyst[edit | edit source]

Ni(pbi)(pyS)2 Ni(pbt)(pyS)2

Photosensitizer[edit | edit source]

Eosin Y

Investigation[edit | edit source]

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

Ni(pbi)(pyS)2

0.004

Eosin Y

2

TEOA

0.4

H2O

14000
2.

Ni(pbt)(pyS)2

0.004

Eosin Y

2

TEOA

0.4

H2O

13100
Investigation-Name: Table 1

Sacrificial Electron Donor[edit | edit source]

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

Additives[edit | edit source]

In this study, no additives were tested.

Investigations

  • Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)