Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer: Difference between revisions

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DOI 10.1016/j.apcata.2016.04.035
Authors Jun-Xiao Zhang, Chang-Ying Hu, Wei Wang, Hui Wang, Zhao-Yong Bian,
Submitted 08.05.2016
Licenses https://www.elsevier.com/tdm/userlicense/1.0/,
Subjects Process Chemistry and Technology, Catalysis
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{{#doiinfobox: 10.1016/j.apcata.2016.04.035}}
{{DOI|doi=10.1016/j.apcata.2016.04.035}}
[[Category:Photocatalytic CO2 conversion to CO]]
[[Category:Photocatalytic CO2 conversion to CO]]
[[Category:Photocatalytic CO2 conversion to HCOOH]]
[[Category:Photocatalytic CO2 conversion to HCOOH]]
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=== 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 CO and HCOOH using different ratios of the catalyst and photosensitizer. The catalytic system performed best for the catalyst:photosensitizer ratio of 4:1.  
The article contains results for the reduction of CO<sub>2</sub> to CO and HCOOH using different ratios of the catalyst and photosensitizer. The catalytic system performed best (referring to the TONs of CO and HCOOH production) for the catalyst:photosensitizer ratio of 4:1.  


==== Catalyst====
==== Catalyst====
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==== Additives ====
==== Additives ====
In this study, no additives were used.
In this study, no additives were used.[[Category:Publication]]

Latest revision as of 10:37, 11 April 2024


Abstract[edit | edit source]

Summary[edit | edit source]

A photochemical reduction of CO2 was shown using the manganese catalyst Mn(bpy)(CO)3Br and the zinc photosensitizer ZnTPP. Turnover numbers (TONs) of 64 and 16 were reached after 180 min of irradiation for CO and formic acid, respectively. The experiments were performed using a Xenon lamp as the light source.

Advances and special progress[edit | edit source]

Photochemical CO2 conversion in an environmentally friendly and sustainable photocatalytic system using earth abundant metal complexes efficiently yielded CO and HCOOH in aqueous acetonitrile solution.

Additional remarks[edit | edit source]

The manganese catalyst and the zinc photosensitizer were used in different ratios, resulting in different TONs for CO and HCOOH production.

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

The article contains results for the reduction of CO2 to CO and HCOOH using different ratios of the catalyst and photosensitizer. The catalytic system performed best (referring to the TONs of CO and HCOOH production) for the catalyst:photosensitizer ratio of 4:1.

Catalyst[edit | edit source]

Mn(bpy)(CO)3Br

Photosensitizer[edit | edit source]

ZnTPP

Investigation[edit | edit source]

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

Mn(bpy)(CO)3Br

2

ZnTPP

0.5

TEA

0.1

MeCN

xenon lamp11919
2.

Mn(bpy)(CO)3Br

1.5

ZnTPP

0.5

TEA

0.1

MeCN

xenon lamp9718
3.

Mn(bpy)(CO)3Br

0.5

ZnTPP

0.25

TEA

0.1

MeCN

xenon lamp6416
4.

Mn(bpy)(CO)3Br

0.5

ZnTPP

0.5

TEA

0.1

MeCN

xenon lamp1210
5.

Mn(bpy)(CO)3Br

0.5

ZnTPP

1

TEA

0.1

MeCN

xenon lamp86
6.

Mn(bpy)(CO)3Br

0.5


TEA

0.1

MeCN

xenon lamp21
7.


ZnTPP

0.5

TEA

0.1

MeCN

xenon lamp
Investigation-Name: Table 1

Sacrificial electron donor[edit | edit source]

In this study, triethylamine (TEA) was used as sacrificial electron donor.

Additives[edit | edit source]

In this study, no additives were used.

Investigations

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