Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center

Abstract

Summary

A photochemical reduction of CO₂ to CO or formic acid was shown using the iron complexes [Fe(pabop)Cl2][CLO4] (100755) or [Co(pabop)][ClO4]2 (100759) as catalysts in combination with the iridium-based photosensitizer Ir(ppy)3 (100843). Turnover numbers (TONs) over xx and a selectivity of xx% for CO were reached in xx. The experiments were conducted under visible-light irradiation (λ = xx nm) using TEA as sacrificial reductants (see section SEDs below).

Content of the published article in detail

The article contains results for the reduction of CO₂ to CO and formic acid under visible-light catalysis using iron complexes as catalysts. The catalytic system performs best (referring to the TON of CO production) in xx.

Catalyst

[Fe(pabop)Cl2][CLO4] (100755) [Co(pabop)][ClO4]2 (100759)

Photosensitizer

Ir(ppy)3 (100843)

Investigation

		cat	cat conc [µM]	PS	PS conc [mM]	e-D	solvent A	.	.	λexc [nm]	.	TON CO	TON HCOOH	.	.
(edit)	1.	[Co(pabop)][ClO4]2	0.05	Ir(ppy)3	0.2	TEA	MeCN			>460		270
(edit)	2.	[Fe(pabop)Cl2][CLO4]	0.05	Ir(ppy)3	0.2	TEA	MeCN			>420			5

Investigation-Name: Table 1

Sacrificial electron donor

In this study, the experiments were done with the sacrificial electron donor TEA (100505).

Additives

In this study, no additives were tested.