Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163471
Title: Cobalt quaterpyridine complexes for highly efficient heterogeneous CO₂ reduction in aqueous media
Authors: Sun, Libo
Reddu, Vikas
Xi, Shibo
Dai, Chencheng
Sheng, Yuan
Su, Tan
Fisher, Adrian C.
Wang, Xin
Keywords: Engineering::Chemical engineering
Issue Date: 2022
Source: Sun, L., Reddu, V., Xi, S., Dai, C., Sheng, Y., Su, T., Fisher, A. C. & Wang, X. (2022). Cobalt quaterpyridine complexes for highly efficient heterogeneous CO₂ reduction in aqueous media. Advanced Energy Materials, 12(34), 2202108-. https://dx.doi.org/10.1002/aenm.202202108
Project: M4012076 RG118/1 
A1983c0026 
Journal: Advanced Energy Materials 
Abstract: Ligands play a critical role in the electrocatalytic CO2 reduction reaction (CO2RR) based on heterogeneous molecular catalysts. Previous research on heterogeneous molecular electrocatalysis has mainly dealt with N4 ligands with pyrrole as subunits (porphyrin, phthalocyanine, etc.), while ligands constructed from pyridine subunits remain uncommon. The examples for comparing active configurations are few and far between. Herein, the development of new N4 cobalt complexes based on pyridine subunits is explored. After anchoring onto carbon nanotubes, they can exhibit CO2RR activity at a low overpotential of 140 mV, and high activity from -0.30 to -0.60 V versus reference hydrogen electrode with a selectivity of above 98%. Excellent performance at large current densities can also be observed in a flow cell. In situ attenuated total reflectance-Fourier transform infrared spectroscopy proves that such electrocatalysts exhibit CO production at lower overpotential and moderate CO adsorption ability over a wide potential range. From density functional theory calculations, it is shown that a pyridine-based cobalt complex on a carbon substrate can reduce the Gibbs free energy for reactions further than its counterpart pyrrole-based ones. Further analysis proves that the semimetal behavior of optimized d-orbitals may facilitate charge transfer and increase the activity. This provides a new insight for understanding catalytically active moieties in heterogeneous molecular catalysts with ligands constructed from pyridine subunits.
URI: https://hdl.handle.net/10356/163471
ISSN: 1614-6832
DOI: 10.1002/aenm.202202108
Rights: © 2022 Wiley-VCH GmbH. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MSE Journal Articles
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