Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction/Photocatalytic CO2 reduction under varied conditions: Difference between revisions

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< Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction
investigation
Molecular process, Photocatalytic CO2 conversion experiments
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{{Photocatalytic CO2 conversion experiments
{{Photocatalytic CO2 conversion experiments
|experiments={{Photocatalytic CO2 conversion
|experiments={{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|e-D=Molecule:100508
|e-D=Molecule:100508
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806
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|include=Yes
|include=Yes
}}{{Photocatalytic CO2 conversion
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100650
|catalyst=Molecule:100823
|cat conc=0.1
|cat conc=0.1
|PS=Molecule:100806
|PS=Molecule:100806

Revision as of 11:36, 28 November 2023

cat cat conc [µM] PS PS conc [mM] e-D e-D conc [M] H-D H-D conc [M] solvent A solvent B solvent C solv A/B/C additives additives conc [M] feedstock gas feedstock volume intensity pH T [°C] λexc [nm] t [h] TON CO TOF CO Φ CO [%] TON CH4 TOF CH4 Φ CH4 [%] TON H2 TOF H2 Φ H2 [%] TON HCOOH TOF HCOOH Φ HCOOH [%] TON MeOH TOF MeOH Φ MeOH [%] selectivity [%] [CO;CH4;H2;HCOOH;MeOH] Φ all [%] Details include

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



TEA solar spectrum 10.6 n/a


Yes

Molecule:100673

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



TEA solar spectrum 0.1 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


DMF



TEA solar spectrum 9 n/a


Yes

Molecule:100673

0.1

Molecule:100806

0.1

BIH

0.011


DMF



TEA solar spectrum 0.5 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



solar spectrum 1.8 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



proton sponge solar spectrum 5.6 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



TfOH solar spectrum 0.9 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1


BIH

0.011


MeCN



TEA solar spectrum 0.6 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1



MeCN



TEA solar spectrum 0.3 n/a


Yes

Ni(4O(-)py)-(MeNHC)2Cl

0.1

Molecule:100806

0.1

BIH

0.011


MeCN



N2 solar spectrum 0.2 n/a


Yes