An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor: Difference between revisions

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< An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
investigation
Molecular process, Photocatalytic CO2 conversion experiments
(Created page with "{{Photocatalytic CO2 conversion experiments |experiments={{Photocatalytic CO2 conversion |catalyst=Molecule:100760 |PS=Molecule:100808 |e-D=Molecule:100507 |solvent A=Molecule:100529 |solvent B=Molecule:100507 |solvent-ratio=4:1 |include=No }} }}")
 
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|solvent B=Molecule:100507
|solvent B=Molecule:100507
|solvent-ratio=4:1
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=4.25
|TON HCOOH=25
|Φ HCOOH=85
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100529
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=5.75
|TON HCOOH=25.75
|Φ HCOOH=82
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100529
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=5.25
|TON HCOOH=27
|Φ HCOOH=84
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100529
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=5.75
|TON HCOOH=19
|Φ HCOOH=77
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100505
|solvent A=Molecule:100529
|solvent B=Molecule:100505
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=2
|TON HCOOH=12.5
|Φ HCOOH=86
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100505
|solvent A=Molecule:100529
|solvent B=Molecule:100505
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=2.75
|TON HCOOH=14.5
|Φ HCOOH=84
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100505
|solvent A=Molecule:100529
|solvent B=Molecule:100505
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=1
|TON HCOOH=10.25
|Φ HCOOH=91
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100505
|solvent A=Molecule:100529
|solvent B=Molecule:100505
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=16.25
|TON HCOOH=11.25
|Φ HCOOH=41
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100531
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=3.25
|TON HCOOH=20.5
|Φ HCOOH=86
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100531
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=water
|λexc=405 nm
|irr time=24
|TON H2=3.5
|TON HCOOH=24
|Φ HCOOH=87
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100531
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=7.75
|TON HCOOH=30
|Φ HCOOH=79
|include=No
}}{{Photocatalytic CO2 conversion
|catalyst=Molecule:100760
|PS=Molecule:100808
|e-D=Molecule:100507
|solvent A=Molecule:100531
|solvent B=Molecule:100507
|solvent-ratio=4:1
|additives=phenol
|λexc=405 nm
|irr time=24
|TON H2=9
|TON HCOOH=34.75
|Φ HCOOH=79
|include=No
|include=No
}}
}}
}}
}}

Revision as of 17:37, 23 January 2024

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

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMF

TEOA


4:1 water 405 nm 24 4.25 25 85 0%; 0%; 14.5%; 85.5%; 0%

85

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMF

TEOA


4:1 water 405 nm 24 5.75 25.75 82 0%; 0%; 18.3%; 81.7%; 0%

82

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMF

TEOA


4:1 phenol 405 nm 24 5.25 27 84 0%; 0%; 16.3%; 83.7%; 0%

84

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMF

TEOA


4:1 phenol 405 nm 24 5.75 19 77 0%; 0%; 23.2%; 76.8%; 0%

77

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEA


DMF

TEA


4:1 water 405 nm 24 2 12.5 86 0%; 0%; 13.8%; 86.2%; 0%

86

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEA


DMF

TEA


4:1 water 405 nm 24 2.75 14.5 84 0%; 0%; 15.9%; 84.1%; 0%

84

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEA


DMF

TEA


4:1 phenol 405 nm 24 1 10.25 91 0%; 0%; 8.9%; 91.1%; 0%

91

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEA


DMF

TEA


4:1 phenol 405 nm 24 16.25 11.25 41 0%; 0%; 59.1%; 40.9%; 0%

41

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMA

TEOA


4:1 water 405 nm 24 3.25 20.5 86 0%; 0%; 13.7%; 86.3%; 0%

86

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMA

TEOA


4:1 water 405 nm 24 3.5 24 87 0%; 0%; 12.7%; 87.3%; 0%

87

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMA

TEOA


4:1 phenol 405 nm 24 7.75 30 79 0%; 0%; 20.5%; 79.5%; 0%

79

No

[Re(bpy)2(CO)2][OTf]

[Ru(bpy)3][PF6]

TEOA


DMA

TEOA


4:1 phenol 405 nm 24 9 34.75 79 0%; 0%; 20.6%; 79.4%; 0%

79

No