Boosting CO<sub>2</sub> Electroreduction via the Synergistic Effect of Tuning Cationic Clusters and Visible-Light Irradiation.
basic_science · Level V
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- Record sourced from PubMed, PMID 34050558.
- Also identified by DOI 10.1002/adma.202101886.
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Abstract
Introducing an external light field can increase the intrinsic activity and energy efficiency for electrochemical CO<sub>2</sub> reduction. Herein, a synergistic strategy that introduces photosensitive components and visible light into a stable system is reported to improve the performance for CO<sub>2</sub> reduction. The catalytic kinetics studies indicate that the synergistic effect of implantation of cationic Ti and additional light driving is the primary responsibility for accelerating the first electron transfer to form a *COO<sup>-</sup> intermediate. This leads to a satisfactory CO<sub>2</sub> -to-CO conversion for Zr/Ti-NB-Co in terms of high selectivity (Faradaic efficiency of 93.6% at -0.7 V), remarkable catalytic activity (production rate up to 546 mmol g<sup>-1</sup> h<sup>-1</sup> at -1.1 V), excellent long-term stability (without performance decay over 11 h), and large turnover frequency of 1028 h<sup>-1</sup> at -1.1 V under visible light. These results imply that the photodriven Ti-based porphyrin catalyst not only can deliver more electrons, but also can act as a photoswitch to adjust the electron transfer pathway.